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Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process?.Our Client, a global leading Biotech company is looking for a Clinical Specialist/Junior Clinical Research Associate.Conduct site evaluation and setup for SCENESSE® commercial distr

Purpose Describe the primary goals objectives or functions or outputs of this position. The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages. The Study Project Manager I is responsible for and ensures clinical research studies are executed with quality and efficiency on-time within budget and meet company objectives. The Study Project Manager I achieves these objectives by bringing scientific acumen strategic thinking innovation experience in clinical study operations management and stakeholder management to address risks and challenges. The Study Project Manager I serves as leader of one or more cross functional Clinical Study Teams leading clinical operations from planning through to execution in a cross functional matrix environment. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. • On a given study responsible for (but not limited to) : • the development of the clinical study design and associated systems tools and documents, • study budget creation and oversight, • vendor selection scope development management and oversight of external vendors, • Proactively identifying risks and address and/or escalate study related issues and opportunities for efficiency, • Empowered decision maker on operational aspects of study execution. • creating an inclusive and innovative environment where staff and studies/programs will succeed, • Provide leadership to Study Management Associates lead delegate and support activities to deliver on study milestones Qualifications : Qualifications List required and preferred qualifications (up to 10). Include education skills and experience. • Bachelors Degree or equivalent degree is required 6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required. Preferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience Additional Information : Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. * This job is eligible to participate in our long-term incentive programs Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary The Manager R&D Data Stewardshipsupports the implementation of data stewardship activities by maintaining data standards monitoring data quality and managing stewardship tools and documentation. Works closely with data owners IT and scientific teams to ensure consistent application of data quality rules and high-quality data management practices. Main Responsibilities: * Maintain and update data dictionaries metadata repositories and data management documentation. * Perform data curation and wrangling activities to deliver accurate standardized and metadata enriched data for downstream scientific/data science analytics or integration into data platforms. * Resolve data issues discrepancies and prevent duplication or corruption. * Perform regular data quality checks track issues and support remediation efforts. * Curate metadata and business glossaries to make data meaningful and discoverable. * Provide training and guidance on data management best practices. * Provide end-user support for data management tools (e.g. central data repositories metadata catalogue data quality dashboards). * Collaborate with IT and data owners to ensure smooth integration of data management practices into data platforms and scientific systems. * contribute to process improvements by identifying opportunities for enhanced data quality or efficiency. Qualification: * Bachelors degree in Life Sciences Information Sciences or related field. * 4-6 years of experience biomedical R&D data management or related roles. * Experience managing data across Research Clinical Safety and/or Regulatory domains. * Understanding of FAIR data principles and regulatory requirements. * Understanding of data quality concepts and metadata management and governance principles. * Experience working with data and scientific platforms and basic data analysis tools. * Strong attention to details documentation and communication skills. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Associate Director Site Management & Monitoring Oversight Lead is responsible for clinical operations strategic leadership to ensure conduct and oversight of monitoring and site management of clinical programs in the designated region following our strategy appropriate international regulatory standards and within the agreed timeframe and budget. This role will be the strategic interface between therapeutic areas and study management to ensure the quality of the delivery of the clinical program(s) at the site level. The Associate Director will oversee the permanent and functional service provider site management staff and build a strategic relationship with service providers and CROs at a regional level. Main Responsibilities and Accountabilities Strategic Leadership & Oversight • Lead regional clinical operations strategy aligned with global clinical development goals., • Ensure monitoring and site management activities meet international regulatory standards timelines and budget targets., • Oversee the quality and consistency of clinical program execution at the site level. Vendor & CRO Management • Build and maintain strategic relationships with service providers and CROs., • Oversee permanent and functional service provider staff involved in site management. Operational Excellence • Drive continuous improvement in site performance and monitoring practices., • Identify and mitigate risks to ensure smooth clinical trial execution. Cross-Functional Collaboration • Collaborate with internal stakeholders across clinical development regulatory and data management., • Ensure alignment between regional execution and global clinical strategy. Compliance & Governance • Ensure adherence to GCP ICH and applicable regulatory requirements., • Support audit readiness and inspection preparedness across regional sites. In addition • Act as the primary point of contact both internally and externally (e.g. vendors) as applicable for anything study related., • Maintain up to date knowledge of the therapeutic area/product candidate(s) clinical practice competitors and regulatory considerations., • Support audits/inspections and resolutions of findings., • Support in the development of new SOPs guidelines etc and/ or participate in working groups about new processes., • Functional leadership and mentorship of junior staff required; Act in advisory capacity to other clinops colleagues within and across TAs., • When accountable to a set of studies and/or program (s) provides oversight and direction ensuring appropriate delegation and delivery inter-program efficiencies and applied learnings. Job Qualifications and Experience Requirements Education At minimum bachelors degree or equivalent in life science nursing pharmacy medical laboratory technology or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g. diploma or associate degree RN certified medical technologist). Experience • As a guide a minimum of 10 years relevant clinical research (or related) experience within the pharmaceutical industry., • Previous experience in leading and managing a team of professional staff., • A solid understanding of the drug development process and specifically each step within the clinical trial process., • Experience in site management and monitoring and overseeing large and/or complex global clinical trials., • Robust budget forecasting and management experience., • Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Competencies • Demonstrated ability to lead teams and work in a fast-paced team environment., • Experienced in working within a Matrix Environment and ability to work through interpersonal difficulties and resolve conflicts with a Matrix Environment, • Successfully demonstrated the ability to mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities., • Ability to evaluate judge and make decisions regarding staff. Ability to teach/coaching and setting an example of best practice., • Excellent interpersonal and decision-making skills., • Demonstrates innovation. Possesses drive energy and enthusiasm to deliver the program objectives., • Skilled at independently navigating new or novel indications study/program approaches and unique challenges., • Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report., • Ability to plan and ensure execution and completion of clinical program(s) to the highest ethical and scientific standards., • Extensive and comprehensive knowledge of ICH guidelines/ GCP Maintains current medical/scientific/regulatory knowledge., • Demonstrated project management skills including simultaneous management of multiple projects. Possesses excellent planning time management & coordination skills., • Demonstrated ability to problem solve and use clear judgment in relation to interactions with external parties timelines and complex clinical programs., • Excellent written and oral communication skills and maintains computer literacy in appropriate software. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

• Office based in Maidenhead (hybrid working model 3 days in office), • Reporting to the Head of Medical Operations In this role you will provide leadership oversight and be accountable for the generation of high-quality real-world evidence studies to optimise and enhance the product and/or therapeutic value propositions across the AbbVie portfolio. Strong cross-functional alignment with the Medical Market Access (including HTA Health Economists Asset leads Strategic Partnership Leads) Brand Teams both within affiliate and Globally will be required to generate high quality evidence to demonstrate value for AbbVie medicines. The Medical and Outcomes Research Lead will proactively collaborate and engage with external parties (NHS and vendors) as well as representing AbbVie on all RWE related engagements. Key Responsibilities • Lead and oversee all research projects within the UK Affiliate Local Evidence Team, • Manage and develop a team of Medical Outcomes and Research Managers/Specialists to generate real world data, • Shape and optimize processes policies and methods for conducting effective real-world evidence (RWE) studies, • Maintain and provide up-to-date expertise in RWE across AbbVie products and therapeutic areas; deliver training to stakeholders, • Source generate interpret and disseminate high-quality evidence to internal and external customers and support product submissions to external agencies (e.g. NICE SMC), • Design and manage RWE and outcomes research studies from concept through approval to execution in collaboration with medical advisors and operations, • Facilitate clear communication with cross-functional teams on study progress and challenges, • Ensure research studies are delivered on time and within budget in line with operational plans, • Support alignment of study protocols from Global and European teams with UK affiliate needs and timelines, • Foster strong relationships with Global/Europe teams lead or contribute to regional outcomes research initiatives and support publication and dissemination strategies for RWE findings Qualifications : Experience Required • Graduate qualification in Evidence Based Medicine Real World Evidence Outcomes Research Epidemiology Public Health Medical or a life Science degree preferred or professional scientific background, • Experience in pharmaceutical/biotechnological industry in a scientific/medical or Market Access role with experience in RWE Outcomes Research Epidemiology, • Knowledge of Good Clinical Practice (GCP) pharma industry standards global & local Standard Operating Procedures (SOPs), • Solid understanding of clinical and statistical research methods; searching collating analyzing and interpreting data from various data sources to supplement clinical trial data sets, • Working knowledge of primary data collection methodologies such as prospective data registries or longitudinal cohort studies patient and caregiver surveys or pragmatic clinical trialsExcellent medical knowledge in relevant therapeutic areas of AbbVie products, • Experience of and strong ability to work collaboratively across matrix functions, • Establish strong professional relationships with all stakeholders inside the company, • Capability to manage complex information and work to strict timelines, • Ability to translate complex concepts into simple language and communicate with non-experts, • Rapidly adaptable to a fast-changing environment and willingness to assess and implement new ideas and opportunities, • Sound judgment strong planning and organizational skills and the ability to get things done, • Leadership line management and development of direct reports, • Looks outside AbbVie for new ideas to stimulate innovation, • Rapidly build strong strategic partnerships outside AbbVie, • Lead with a strong compliance mindset to meet our SOP requirements Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The role Were looking for a Drug Development Project Manager someone who understands how discovery turns into development and development turns into real therapies for patients. This is not a generic project management position; its about driving the scientific technical and operational progress that determines whether a potential medicine succeeds. Youll be the connection between scientific strategy and operational delivery coordinating complex global programmes that draw on expertise from discovery clinical regulatory CMC and commercial functions. Your focus will be keeping teams aligned assessing scenarios and making decisions in a timely fashion. This ensures that every milestone moves us closer to patients who need new treatment options. Why this job This role sits along the central axis of some of CSLs most strategically important development programmes the kind of projects where coordination and clarity make the difference between momentum and delay. Its an opportunity to work at the point where science strategy and execution meet; to see the bigger picture while ensuring every moving part is in sync. For an experienced drug development project manager this is the chance to apply your skills where they truly shape outcomes not just track them. CSL is at an inflection point. Were undergoing a massive transformation in R&D. It represents a tremendous opportunity to be involved to work with key decision makers and have influence on project progression. We have exciting new assets coming out of our research portfolio as well as an existing portfolio of medicines which were looking into further transforming to improve the quality of patients lives What youll do • Translate project strategy into executable plans with clear timelines budgets and risk management., • Lead and motivate multidisciplinary teams across discovery clinical regulatory and CMC., • Anticipate challenges evaluate scenarios and keep teams aligned on critical path activities., • Present concise updates and recommendations to senior stakeholders., • Coach and mentor colleagues in project management best practice and delivery discipline. What youll bring • Bachelors degree or equivalent in science engineering or related discipline (advanced degree preferred)., • 7 years in biotech or pharmaceutical R&D including 5 years managing cross-functional programmes., • Broad understanding of drug development clinical CMC and regulatory processes., • Demonstrated success in delivering projects on time within budget and to agreed quality standards., • Excellent communication and influencing skills; ability to work effectively across cultures and time zones., • Strong proficiency in project management tools and methodologies (e.g. Microsoft Project PMP certification advantageous). Join us if you want to combine scientific curiosity with disciplined delivery helping shape the therapies that make a lasting difference for patients around the world. CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits from health care to financial protection so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family need help paying for emergency back up care or summer camp looking for mental health resources planning for your financial future or supporting your favorite charity with a matching contribution CSL has many benefits to help achieve your goals. Please take the time to review our ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Senior Site Management and Monitoring Oversight Lead is accountable for the strategic and operational oversight of investigational site management and monitoring activities across assigned clinical studies or programs. This role ensures that clinical trials are executed with high quality regulatory compliance and operational efficiency in alignment with global clinical development strategies. Operating within a matrix environment this role partners with internal stakeholders and external service providers to develop and implement study-specific oversight plans monitor site performance and proactively identify and mitigate risks. The role is pivotal in maintaining sponsor oversight validating the effectiveness of site-level activities and ensuring that monitoring plans and tools adequately address protocol-specific risks. Main Responsibilities and Accountabilities: Site Oversight Execution • Ensure effective sponsor oversight of investigational sites by reviewing monitoring visit reports site communications and issue resolution documentation. Monitoring Plan Implementation • Support the development and execution of study-specific monitoring plans ensuring alignment with protocol requirements and risk-based monitoring strategies. Performance Tracking • Monitor site-level performance metrics (e.g. enrollment data quality protocol adherence) and escalate concerns to study leadership as needed. Vendor Collaboration • Partner with CROs and external service providers to ensure consistent and compliant site management practices across assigned studies. Compliance & Inspection Readiness • Contribute to audit and inspection preparedness by validating site documentation ensuring timely issue resolution and maintaining oversight logs. In addition • Act as the primary point of contact both internally and externally (e.g. vendors) as applicable for anything study related., • Maintain up to date knowledge of the therapeutic area/product candidate(s) clinical practice competitors and regulatory considerations., • Support audits/inspections and resolutions of findings., • Support in the development of new SOPs guidelines etc and/ or participate in working groups about new processes., • Mentor and training more junior staff on processes and procedures. Job Qualifications and Experience Requirements: Education At minimum bachelors degree or equivalent in life science nursing pharmacy medical laboratory technology or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g. diploma or associate degree RN certified medical technologist). Experience • As a guide a minimum of 7 years relevant clinical research (or related) experience within the pharmaceutical industry., • Previous experience in leading and managing a team of professional staff., • A solid understanding of the drug development process and specifically each step within the clinical trial process., • Experience in site management and monitoring and overseeing large and/or complex global clinical trials., • Robust budget forecasting and management experience., • Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Competencies • Demonstrated ability to lead teams and work in a fast-paced team environment., • Experienced in working within a Matrix Environment and ability to work through interpersonal difficulties and resolve conflicts with a Matrix Environment, • Successfully demonstrated the ability to mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities., • Ability to evaluate judge and make decisions regarding staff. Ability to teach/coaching and setting an example of best practice., • Excellent interpersonal and decision-making skills., • Demonstrates innovation. Possesses drive energy and enthusiasm to deliver the program objectives., • Skilled at independently navigating new or novel indications study/program approaches and unique challenges., • Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report., • Ability to plan and ensure execution and completion of clinical program(s) to the highest ethical and scientific standards., • Extensive and comprehensive knowledge of ICH guidelines/ GCP Maintains current medical/scientific/regulatory knowledge., • Demonstrated project management skills including simultaneous management of multiple projects. Possesses excellent planning time management & coordination skills., • Demonstrated ability to problem solve and use clear judgment in relation to interactions with external parties timelines and complex clinical programs., • Excellent written and oral communication skills and maintains computer literacy in appropriate software. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

We at TFP are looking for brilliant minds and passionate hearts to help us shape the future of fertility. We are one of the largest fertility service providers in Europe operating our IVF clinics and egg/sperm freezing banks in the UK Poland and Netherlands. We have embarked on the mission to use technology to provide patients with a memorable best-in-class fertility journey that leads to the best outcome starting a family! At TFP we offer all our patients the care understanding and expertise that help to bring dreams to life. We are passionate about what we do which reflects our commitment to creating lives and changing lives. Science research and innovation are key to how we work and have led to us pioneering fertility treatment for more than 35 years. Many of our clinicians are internationally renowned specialists and we regularly share knowledge across our clinics to further improve our success. Join us at TFP Fertility where your passion and expertise can contribute to our legacy of excellence. The Role: The post-holder will be one of a group of specialist nurses working within the fertility clinic. Treatments range from IVF and ICSI Ovulation Induction Egg donation and Sharing Egg Recipiency and Surgical Sperm Retrieval. This role is full time working 37.5 hour per week- weekends on rotation are required Part time options will be considered for the successful candidate if required The Location: Thames Valley Fertility (TVF) was established in 2017 and due to the passion expertise and reputation of our team has already grown into a leading fertility clinic. Providing treatment to both NHS and private patients TVF performs approximately 550 fresh cycles and 450 frozen cycles per year. Offering a full suite of treatment and diagnostic services including PGT. Conveniently located on the outskirts of Maidenhead adjacent to junction 8/9 of the M4 there is ample free parking for staff and patients at the front of the building. TVF also has a 5/5 inspection rating from the HFEA Key Responsibilities: * To develop a satisfactory level of clinical competence in ART skills e.g. plan and co-ordinate treatment cycles to undertake specific investigations such as endocrine profiles. * To assist in the management and support of sub-fertile couples before during and after treatment cycles developing a therapeutic environment to meet the individual needs of the couples. * To undertake patient consultations before during and post treatment cycles. * To ensure that informed consent is given and the appropriate unit and Human Fertilisation Embryology Authority consent forms are completed for the treatment cycle discussing the risks associated with ART and potential usage of gametes for research. * To demonstrate excellent communication skills providing information and implications counselling to enable couples to make informed choices regarding their treatment * To demonstrate use of excellent communication skills to support patients and families in highly stressful situations (e.g. breaking bad news diagnosis of ectopic or miscarriage managing bereavement and anger management) both face to face and over the telephone. * To ensure through the process of implications counselling that all couples are aware of the risk of iatrogenic disease such as ovarian hyper-stimulation multiple pregnancy (with risk of prematurity and death) and the complex issue of research on gametes/embryos and the ethical and moral issues that this raises. * To explain and complete consent forms for the storage of frozen gametes and the posthumous use thereof for all couples freezing spare gametes with the implications of disposal of property in the event of separation or divorce. * To keep accurate records for each patient of all communication both and clinical activity relevant to his/her treatment in line with NMC regulations. To help with the production of written information to meet the changing expectation of the needs of the couples/patients. * To assist with the collation of all data resulting from the procedures and transfer this to the records on the computer and into the patient notes to satisfy HFEA regulations. * In conjunction with senior nursing staff to be responsible for the booking of the patients treatment cycle planning drug prescribing and liaising with GPs. * To explain the individualised treatment schedule including the potential side effects of the drug treatment and demonstration of injection technique with the use of subcutaneous injection pen. * To co-ordinate oocyte retrieval and embryo transfer/intrauterine insemination donor insemination provide appropriate counselling support and advice with cycle outcome. * To demonstrate skill at interpreting complex clinical information/data anticipating potential problems taking action to prevent/minimise these responding to any changes promptly and effectively and developing specialised plans of care / following the relevant protocols. * To demonstrate dexterity accuracy and attention to detail in the preparing of specialist equipment for procedures to be undertaken within the unit/ward whilst adhering to Local policies e.g. intravenous drug administration. Taking blood samples catheterisation etc and to ensure that staff are trained and supported to develop these skills. To promote the highest standards of cleanliness and sterility of all equipment used in the IVF guided egg retrieval saline ultrasound embryo transfer and intra-uterine insemination procedures in line with HFEA practice. * To supervise and assist in the preparation and care of the patient and her partner before during and after the above procedures. * To demonstrate initiative and provide support in assisting medical staff with procedures e.g. performing transvaginal ultrasound guided oocyte retrieval. * To work within the legal framework as laid out by the 1990 Human Fertilisation and Embryology Act of Parliament and Care Quality Commission * To manage difficult situations with competence taking appropriate action utilising relevant protocols and supporting the patient their relatives and members of the multidisciplinary team as required. * To ensure that procedures/policies are in place so that emergency /crisis situations are managed with competence and that patients/ relatives and staff members are adequately supported during and after the event. * To ensure COSHH Infection Control Risk Management and maintenance of health and safety within the department is implemented according to unit policy and that every effort is made to identify and minimise potential risks/hazards. * To ensure that all record keeping on the unit is accurate and legible and maintains patient confidentiality according to Trust and HFEA policy. * In conjunction with senior nursing staff to ensure all complaints and grievances are dealt with competently and effectively in line with the units complaints procedure. * To support senior nursing staff with the maintenance of the pharmacy drug stores including controlled drugs in line with Trust policy and Home Office legislation. Experience: * 1st level registration with NMC * Interest in womens health * Computer skills * Phlebotomy * Theatre and recovery Desirable previous experience in the fertility or womens health setting educated to degree level teaching/mentoring qualification sonography experience Salary: Competitive (Depending on experience) Location:TFP Thames Valley Fertility - Maidenhead Working Hours:37.5 hours per week - part time options considered Weekends required at 1:4 Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days Bank holidays Your application has been successfully submitted!

• Home or office based (Maidenhead HQ), • Reporting to Director Health Literacy This position leads strategic development of behavioral science initiatives with cross functional stakeholders in support of health literacy activities for AbbVie Patient Safety to promote clinical trial safety excellence and safe medication use. This includes developing original research protocols to evaluate patient safety data from medication errors product complaints and non-serious adverse events with use of AbbVie products in clinical development and post-market to devise strategies to systemically reduce the incidence of medication errors and improve adherence. This position will act as a health literacy expert for the Product Safety Teams (PSTs) Medical Device Safety Area Product Leads and other functions on the application of health literacy and human factors. This position will be included in strategic decision making on AbbVie products plans to demonstrate real world safety and usability including presenting to senior management. Key Responsibilities • Lead cross-functional teams in the development of novel health literacy programs in collaboration with PSTs Clinical Sciences Clinical Development and other AbbVie functions, • Develop strategy for human-centered design (health literacy activities) and safety assessments to product teams and leadership to inform on necessary medication error reduction, • Evaluate multiple patient level data from multiple sources (clinical trials post-marketing product complaints usability studies) to identify potential gaps that can impact patient safety and develop appropriate mitigations, • Utilizes expert judgment to determine the impact of the safety issue on the products benefit-risk profile including participating in use risk analyses health literacy evaluations and human factors studies to inform product and safety information design, • Lead Patient Safety participation in key product safety activities including clinical trial lay summaries human factors summaries of known use errors and health literacy evaluations of patient-facing materials, • Synthesize evolving global regulatory obligations on medication errors to determine the need for prospective safety data to support new product submissions; work with Asset Strategy Teams to ensure product submission success, • Leads patient-focused drug development and safety-related activities/initiatives for Patient Safety Qualifications : • Degree in a Health Sciences or equivalent clinical/pharma experience, • Demonstrated ability to serve as an expert in behavioral science to cross-functional colleagues by soliciting input and providing strategic guidance, • Experience conducting user testing interviews and analyzing qualitative data, • Proficient in pharmacovigilance regulations guidelines qualitative research and company standard operating procedures Demonstrated effectiveness in working in a multidisciplinary matrix team situation, • Effective oral and written communication skills with the ability to manage multiple projects simultaneously, • Proficient in qualitative research methods Able to work independently with minimal direct supervision Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

Join Our Team and Shape the Future of Clinical Research! At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confidentiality agreements and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency. In this role you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative life-changing medications. Key Responsibilities: In this role you will: * Prepare negotiate and manage site agreements confidentiality agreements and letters of indemnification for clinical trials. * Ensure compliance with SOPs regulatory guidelines and contractual obligations. * Track update and maintain contract status in relevant systems ensuring transparency and timely execution. * Identify and escalate contractual issues to management as needed. * Support the internal review revision and approval process of contracts before forwarding them to external parties. * Collaborate with clinical study teams legal and project management to ensure seamless contract execution. * Maintain electronic and paper contract files ensuring accuracy and accessibility. * Assist in the continuous improvement of departmental processes and procedures. * Provide regular status updates to management and study teams. Required Qualifications: To succeed in this role you should have: * Bachelors degree (LLB JD BA or BS) preferred; a university-level law degree is highly desirable (UK/EU). * Fortrea may consider equivalent relevant experience in lieu of educational requirements. * 24 years of experience in contract negotiation clinical research or a related field. * Strong understanding of ICH GCP guidelines and clinical research processes. * Excellent negotiation communication and organizational skills. * Ability to work independently and manage multiple priorities in a fast-paced environment. * Proficiency in Microsoft Office and contract tracking systems. What We Offer: * Competitive salary and performance-based incentives. * Flexible work arrangements (remote/hybrid options). * Professional growth opportunities in a collaborative and innovative environment. * The opportunity to work on cutting-edge clinical research projects. Ready to Make an Impact Take the next step in your career and join us in driving innovation in clinical research. Apply today! Applications are reviewed on a rolling basisdont miss this opportunity! #LI-Remote #LI-Hybrid Learn more about our ___

Join Our Team and Drive Clinical Research Success! At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory submissions are completed efficiently. Your expertise will help bring life-changing treatments to patients faster. In this role you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative life-changing medications. Key Responsibilities: In this role you will: * Serve as the primary contact for investigative sites during start-up and maintenance activities. * Collect review and organize essential documents required for regulatory submissions (EC/IRB/Third Body/Regulatory Authority). * Ensure compliance with ICH/GCP guidelines regulatory requirements and sponsor specifications. * Prepare and submit regulatory documents including country-specific application forms and informed consent forms. * Track submission timelines and proactively address potential delays. * Collaborate with internal and external stakeholders including vendors clinical teams and regulatory authorities. * Ensure all documentation is audit-ready and systems are consistently updated. * Assist in the negotiation of site contracts and budgets if applicable. * Provide mentorship and training to new hires and less-experienced colleagues. Required Qualifications: To succeed in this role you should have: * University/College degree (life sciences preferred) or certification in a related allied health profession. * Minimum 2 years of experience in clinical research regulatory submissions or site activation. * Strong knowledge of ICH/GCP guidelines RA IRB/IEC regulations and start-up processes. * Ability to review and adapt patient informed consent forms to meet local and protocol-specific requirements. * Experience interacting with regulatory authorities and site start-up teams. * Excellent organizational problem-solving and communication skills. * Proficiency in Microsoft Office and document management systems. * Fortrea may consider relevant and equivalent experience in lieu of educational requirements. What We Offer: * Competitive salary and performance-based incentives. * Flexible work arrangements (remote/hybrid options). * Professional growth opportunities in a collaborative and innovative environment. * The opportunity to work on cutting-edge clinical research projects. Ready to Make an Impact Join us in shaping the future of clinical research. Apply today! Applications are reviewed on a rolling basisdont miss this opportunity! #LI-Remote #LI-Hybrid Learn more about our ___

We at TFP are looking for brilliant minds and passionate hearts to help us shape the future of fertility. We are one of the largest fertility service providers in Europe operating our IVF clinics and egg/sperm freezing banks in the UK Poland and Netherlands. We have embarked on the mission to use technology to provide patients with a memorable best-in-class fertility journey that leads to the best outcome starting a family! At TFP we offer all our patients the care understanding and expertise that help to bring dreams to life. We are passionate about what we do which reflects our commitment to creating lives and changing lives. Science research and innovation are key to how we work and have led to us pioneering fertility treatment for more than 35 years. Many of our clinicians are internationally renowned specialists and we regularly share knowledge across our clinics to further improve our success. TFP has a national donor sperm bank its own quality assurance scheme and own training scheme for junior addition we are proud to say that we offer a clear career framework support continuing professional development and provide opportunities for staff to travel to other TFP clinics further their learning and support career progression. The Locations: Thames Valley Fertility (TVF) was established in 2017 and due to the passion expertise and reputation of our team has already grown into a leading fertility clinic. Providing treatment to both NHS and private patients TVF performs approximately 550 fresh cycles and 450 frozen cycles per year. Offering a full suite of treatment and diagnostic services including PGT. Conveniently located on the outskirts of Maidenhead adjacent to junction 8/9 of the M4 there is ample free parking for staff and patients at the front of the building. Our state- of-the-art laboratory was purpose built in 2017 and is equipped with the latest laboratory equipment and monitoring systems that support us in achieving excellent outcome KPIs. TVF also has a 5/5 inspection rating from the HFEA. Boston Place was established in 2013 and provides treatment to private patients in contemporary surroundings. Boston Place performs approximately 300 fresh cycles and 200 frozen cycles per year and offers a full suite of treatment and diagnostic services whilst specialising in PGT. The clinic is conveniently located adjacent to Marylebone Station in central London. Our state-of-the-art laboratory was purpose built in 2013 and is equipped with the latest laboratory equipment and monitoring systems that support us in achieving excellent outcome KPIs. Boston Place also has a 5/5 inspection rating from the HFEA. The Role: This is an exciting opportunity for a trained Embryologist to join our team of highly skilled and dedicated scientists. As well as providing a significant contribution to the clinical workload the successful candidate will have opportunities to be involved in training junior embryologists internal quality control donor recruitment organising imports/exports and supporting in the management of stored gametes/embryos. This is a full time role working 37.5 hours per week - weekend rotation will be required at approximately 1:4 As part of your role there will be requirement to work between Thames Valley Fertility and Boston Place on a split rota each week. This will be on a 3:2 ratio. Key Responsibilities: Full range of clinical procedures including ICSI & vitrification Communicating with patients about treatment options and results Quality Management assisting with audit & quality control/quality assurance Monitoring/maintaining consumables and equipment. Assisting with the donor recruitment process imports/exports and management of stored gametes/embryos Assisting in training and induction of new and junior staff Regulatory Compliance Qualifications and Experience: Minimum of a degree in Life Sciences an MSc or PhD is preferable HCPC Registered (or immediately eligible) Minimum of 3 years of clinical experience Fully trained in all clinical laboratory procedures preferably including biopsy Good knowledge of the UK Regulatory Framework Must be self-motivated eager to learn and have excellent time management skills. High level of attention to detailed and focused Excellent communication skills Salary: Competitive (Depending on experience) Location:TFP Thames Valley Fertility - Maidenhead TFP and Boston Place Fertility - Marylebone Working Hours:37.5 Monday to Friday 3 days at Thames Valley - 2 days at Boston Place Weekend Working at approximately a 1:4 (renumerated with TOIL/overtime) On-Call: Working approximately a 1:4 in coordination with your weekend (remunerated with a daily rate of pay in addition to your basic salary) Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days Bank holidays (pro rata) Your application has been successfully submitted!

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The incumbent will be responsible for the quality and delivery of high-quality clinical development documents and oversight of clinical study delivery across the portfolio in collaboration with strategic CRO partners. Responsible for overseeing the recruiting staffing and development of the clinical scientists and medical writing specialists in the group. Serve as the decision support lead for the SVP Portfolio Development (PD) and ensure excellence throughout the Portfolio Development organization. Oversight of Individuals * Recruiting staffing training and development of clinical scientists and medical writing specialists in the group to maintain a dynamic and cutting-edge level of medical scientific expertise and advanced drug development approaches Ensuring delivery of high-quality clinical development content including: * Clinical development plans protocols study reports common technical document modules and publications in academic journals * Regulatory submissions and meetings * Stage-gate and benefit risk evaluations and assessments * Presentations at scientific and technical review committees * Implementation of clinical recommendations from all advisory and governance committees Internal interfaces and collaboration * Oversight of and collaboration with partnering functions e.g. Research GRA & Safety POE TES CROs and Medical Writing Vendors * Effecting extensive and collaborative dialogue with TA co-leads to optimize project strategy * Working with Head Clinical Operations to ensure appropriate resourcing to support TA activities and to ensure project planning and execution is aligned with TA Priorities * Maintaining effective oversight of quality in conjunction with appropriate Quality functions External-scientific * Enhancing the reputation of the Company through a culture of scientific integration of the department with academia and other partners through visible publication record KOL Interactions presence at scientific conferences membership of consortia and similar medico-scientific groups builds networks with scientific experts * Ensures that the patient and physician voice is at the forefront in TA strategy development Building a culture of risk taking innovation and peer review across the clinical function Providing clinical scientific leadership throughout CSL Providing support and insight into business development opportunitiesas required Qualifications & Experience Requirements * Experience across all phases of development FIH POC late-stage development and life cycle management * Strong track record of oversight of successful drug development programs * Experience across a wide range of regulatory interactions e.g. filings Ad coms etc * 10yrs of pharma experience in clinical development * Strong personal leadership skills * High level of self-awareness and the awareness of personal impact * Enhanced organizational awareness and the ability to interact and influence from the team level to senior management * Succinct and clear communication style * Extensive experience of leading teams and/or line managing a group(s) We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

Worth Recruiting Property Industry Recruitment Job Title: LETTINGS MANAGER Residential Lettings Location: Maidenhead SL6 Salary: OTE 50000 per annum Position: Permanent Full-Time Reference: WR59400 Join a respected and thriving independent estate agency in Maidenhead as a Lettings Manager. This is a key leadership role for an experienced property professional looking to drive growth manage a high-performing team and oversee all aspects of residential lettings within a sought-after market. Why This Role • Work for a reputable independent agency in a premium market, • Lead a motivated and experienced lettings team, • Strong earning potential with performance-based incentives, • Opportunity to shape the growth of the lettings department, • Manage and grow the residential lettings portfolio, • Lead support and motivate the lettings team, • Conduct valuations and secure new landlord instructions, • Ensure high levels of customer service and compliance, • Drive marketing strategies and local business development, • Handle negotiations tenancy agreements and renewals, • Proven experience in residential lettings at senior level, • Strong leadership and team management skills, • Confident in valuations and winning instructions, • Knowledge of current lettings legislation and compliance, • Exceptional organisational and customer service skills, • Professional driven and results-focused, • Competitive salary with commission/bonus structure, • Autonomy and influence over department direction, • Ongoing training and development, • Work in a prestigious and high-demand area If you are interested in this Lettings Manager role please contact the Property Recruitment Team at Worth Recruiting today quoting reference: WR59400. About Your Application: • Response Time: We receive a great many applications and respond as quickly as possible. If you have not heard from us within 48 working hours please assume that on this occasion your application has not been successful., • Data Protection: Worth Recruiting is acting as a recruitment agency in relation to this position. By submitting your application you consent to Worth Recruiting processing and storing your data for the purposes of your job search. For more information please see our privacy policy on our website., • Confidentiality: All communications with Worth Recruiting are completely confidential. We will always need to speak with you before we are able to submit your CV to our client. Job Reference: WR59400 Lettings Manager Required Experience: Manager Key Skills Google Analytics,Access Control System,Clinical Research,Graphics Design,CSS,Documentation Employment Type : Full-Time Experience: years Vacancy: 1 Yearly Salary Salary: 30000 - 50000

Purpose Provides specialist medical/scientific strategic and operational input for our UK Migraine affiliate into core medical affairs activities such as: healthcare professional/provider interactions (Payers Patients Prescribers and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education data guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities). Works closely with sales marketing and commercial teams to provide strategic medical input into core brand (product) strategies and to support medical/marketing activities (promotional material generation/product launches) and market access. Responsibilities • In cooperation with affiliate / Area Medical teams Marketing RA Clinical and other functional areas provides leadership oversight and support for assigned products/projects., • Establishes and approves scientific methods for hypotheses rational design of affiliate/Area/Global protocols and their reports., • Participation in design and execution of clinical trial safety product safety and risk management plans. May also carry responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review assess and report applicable Adverse Events (AEs) and Serious Adverse Events (SAEs) if assigned to AbbVie conduct on clinical studies., • Oversees the conduct of clinical trials and is medically and scientifically accountable for resolution of safety (AEs & SAEs) issues interpretation of statistical analyses for clinical significance PI selection scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities. NB: All clinical research / development activities for products under development and for post approval commitments such as regulatory agency mandated trials, • or those intended to support product registration or to generate data for label inclusion remain the primary responsibility of TA development teams. Initiates medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy., • Provide scientific/medical education to investigators clinical monitors and Global Project Team members related to therapeutic area or disease specific information. Keeps a breast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource., • Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as the scientific team interface for key regulatory discussions, • May lead cross functional sub teams responsible for discrete projects within the therapeutic area (individual publications or study collaborations), • Initiate research projects and drive them to completion resulting in high quality publications. Ensures budgets timelines compliance requirements are factored into programs scientific activities Qualifications : • Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D. meet requirements) with relevant therapeutic specialty in an academic or hospital environment. Completion of residency and/or fellowship is preferred., • Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3 years of experience is preferred. Proven leadership skills in a cross-functional global team environment. Ability to interact externally and internally to support global business strategy. Ability to run a clinical study or medical affairs team independently with little supervision., • Knowledge of clinical trial methodology regulatory requirements governing clinical trials and experience in development strategy and the design of protocols., • Expert knowledge in a relevant therapeutic specialty., • Ability to interact externally and internally to support global business strategy. Must possess excellent oral and written English communication skills., • For clusters of countries multi-lingual skills of language is preferred. Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

• Office based in Maidenhead (hybrid working model 3 days in office), • Reporting to the Head of Medical Operations The Medical Operations Lead will provide leadership and oversight to ensure medical projects are delivered on time and executed compliantly. • Provides strategic leadership in study operations fostering strong internal and external partnerships to drive and execute innovative ideas across all therapy areas, • Acts as an Affiliate Subject Matter Expert in clinical research and study management collaborating with key stakeholders to deliver Real World Evidence projects that address research gaps, • Oversees resource allocation vendor relationships and financial management for research and publications while continually enhancing user experience and operational efficiency through feedback-driven improvements, • Partner with affiliate Medical Teams to project manage study documents and execute clinical research projects, • Collaborate cross-functionally to translate evidence gaps into Real World Evidence projects from setup to publication, • Manage and develop a team aligning activities with medical priorities and providing training and support, • Allocate resources and oversee workload planning based on team needs, • Supervise development implementation and follow-up of affiliate clinical studies and academic partnerships, • Ensure quality control by defining monitoring and reporting on key quality indicators and driving continuous improvements, • Provide operational input on protocol design eCRF and statistical analysis and support feasibility and ethics submissions, • Oversee data management vendor relationships compliance study tracking and deliverables reporting, • Manage study budgets contracts drug shipments and ensure on-time on-budget delivery through negotiation and process development, • Lead implementation and monitoring of early and compassionate access programs ensuring compliance with regulations and timely protocol reviews Qualifications : Experience Required • Life Sciences Degree or equivalent experience with Project Management qualification desirable, • Experience in a clinical operations function experience working in the pharmaceutical industry, • As an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage, • Understanding of ICH clinical guidelines Business Acumen: • Ability to engage with business partners in a business outcomes and challenges conversation and not just a technical conversation., • Anticipates and recommends technical solutions to business problems., • Establish and maintain high-quality relationships with all levels across the company., • Identified and acknowledged as the single point of contact for UK Medical Research Project needs, • Responsible for maintaining relationships with our third-party vendors and internal and external stakeholders., • Experience in line management Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Director Clinical Operations Lead is accountable for the development of the operational strategy for a clinical study(ies) and/or a clinical program (s) as well as the end-to-end study management and delivery of all operational activities and budget management relating to assigned clinical study (ies)/program(s). Responsibilities encompass support to the development of the operational strategy for our most complex studies and ensuring achievement of all program goals within established timelines budget and quality standards and according to the TA strategies. This role must be experienced in working in a matrix environment (internal and external partners) with cross-functional responsibilities associated with trial execution and overall therapeutic area clinical development planning. Strong communication and presentation skills are required. Main Responsibilities and Accountabilities: • Clinical Operations Strategy: Design and implement operational strategies study management plans and supporting documentation to drive study efficiency and quality (most complex studies). Continuously assess and improve clinical operations processes. Provide early input in CDP and study outline., • Project Management & CRO oversight: Lead cross-functional study teams coordinate with functional area representatives and ensure timely execution of all study-related activities. Responsible for vendor selection/management/oversight issue escalation and inspection readiness., • Stakeholder Management & Team Leadership: Lead and coordinate cross-functional teams fostering collaboration among internal and external stakeholders (including vendors investigators and regulatory authorities). Act as the primary point of contact for all study-related matters build and maintain strong relationships mentor and support team members and represent the study team in communications with senior management. Act in an advisory capacity to other clinops colleagues and ensure knowledge sharing across therapeutic areas. Be the clinops voice at PST/TALT., • Budget Forecasting and Performance Management: Forecast manage and report on study budgets and key performance metrics including study start-up enrollment and data collection timeliness/quality. Engage with key project stakeholders including GPLS TALT leads Finance POE. Drive accuracy and reliability in terms of budget., • End-to-End Clinical Study Management: Plan manage and execute our most complex global clinical studies from protocol development through to Clinical Study Report (CSR) completion and Trial Master File (TMF) archiving. Oversee timelines budgets regulatory/GCP compliance feasibility country strategy enrollment plans and risk mitigation., • Act as the primary point of contact both internally and externally (e.g. vendors) as applicable for anything study/program/asset related., • Provide regular study status updates including critical issues to senior leadership as needed while providing support to the study team with stakeholder management and issue escalation. Portray strong and confident communication and presentation skills. Audiences will include those both internal and external partners., • Support audits/inspections and resolutions of findings., • Contribute to the leadership of the Clinops function in key areas of change and continuous improvement. May be asked to lead cross functional change initiatives. Support in the development of new SOPs guidelines etc and/ or participate in working groups about new processes and change initiatives., • Functional leadership and mentorship of junior staff required; Act in advisory capacity to other clinops colleagues within and across TAs., • Acts as an integral resource for clinops members and ensures that cross-functional process efficiencies are identified and maximized in accordance with project goals and that compliance is maintained. Job Qualifications and Experience Requirements Education At minimum bachelors degree or equivalent in life science nursing pharmacy medical laboratory technology or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g. diploma or associate degree RN certified medical technologist). Experience • As a guide a minimum of 12 years relevant clinical research (or related) experience within the pharmaceutical industry., • Previous experience in leading and managing a team of professional staff., • A solid understanding of the drug development process and specifically each step within the clinical trial process., • Experience in overseeing large and/or complex global clinical trials., • Robust budget forecasting and management experience., • Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Competencies • Demonstrated ability to lead teams and work in a fast-paced team environment., • Experienced in working within a Matrix Environment and ability to work through interpersonal difficulties and resolve conflicts with a Matrix Environment, • Successfully demonstrated the ability to mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities., • Ability to evaluate judge and make decisions regarding staff. Ability to teach/coaching and setting an example of best practice., • Excellent interpersonal and decision-making skills., • Demonstrates innovation. Possesses drive energy and enthusiasm to deliver the program objectives., • Skilled at independently navigating new or novel indications study/program approaches and unique challenges., • Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report., • Ability to plan and ensure execution and completion of clinical program(s) to the highest ethical and scientific standards., • Demonstrated ability to comprehend complex scientific concepts and data. Proficient in reviewing and assessing clinical data., • Extensive and comprehensive knowledge of ICH guidelines/ GCP Maintains current medical/scientific/regulatory knowledge., • Demonstrated project management skills including simultaneous management of multiple projects. Possesses excellent planning time management & coordination skills., • Demonstrated ability to problem solve and use clear judgment in relation to interactions with external parties timelines and complex clinical programs., • Excellent written and oral communication skills and maintains computer literacy in appropriate software. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

Make a meaningful impact by shaping how CSL partners with clinical research sites worldwide. At CSL were driven by a single purpose: to deliver innovative therapies that improve patients lives. The Site Engagement Group plays a key role in achieving this mission by positioning CSL as a sponsor of choice - building strong collaborative and sustainable partnerships with the global clinical sites that make our research possible. As an Associate Director Site Engagement Lead you will be the strategic bridge between CSL and our investigational sites leading initiatives that enhance site satisfaction strengthen collaboration and accelerate clinical trial delivery. Key Responsibilities • Lead site engagement strategy for assigned programs or studies ensuring sites experience seamless coordinated interactions with CSL., • Cultivate strong lasting relationships with key institutions investigators and partner sites to position CSL as a preferred sponsor., • Identify and onboard new strategic sites aligned with CSLs pipeline and country-specific priorities., • Analyze and share site intelligence - turn data into actionable insights that inform feasibility site selection and recruitment strategies., • Evaluate and enhance site satisfaction using feedback to continuously improve engagement approaches and operational processes., • Provide deep market and clinical insights into standards of care patient pathways healthcare systems and regional regulatory landscapes., • Partner cross-functionally with Clinical Trial Management Clinical Development Site Management Feasibility & Start-up Medical Affairs and other internal teams to optimize study execution and strengthen CSLs reputation among HCPs. About You • Advanced degree in life sciences pharmacy or a related health field (PhD or PharmD preferred)., • 12 years of relevant clinical research or related experience (e.g. Clinical Operations Medical Affairs or MSL roles)., • At least 2 years of international Clinical Trial Management experience within a sponsor or CRO environment., • Proven ability to analyze complex data extract key insights and present them compellingly to senior stakeholders., • Skilled in building partnerships across diverse cultures and geographies., • Strong understanding of the full drug development lifecycle and operational realities of clinical trial delivery., • Creative & strategic thinker with hands-on problem-solving ability - comfortable operating in a dynamic fast-paced global environment., • Influential communicator and collaborator who thrives in cross-functional settings., • High ethical standards integrity and a team-oriented mindset., • Willingness to travel (up to 30% regional and international). Why Join CSL At CSL youll have the opportunity to: • Be part of a global mission-driven organization that values science integrity and collaboration., • Shape how CSL engages with clinical research sites improving experiences for investigators and patients alike., • Work with passionate experienced professionals across the globe in a culture that values innovation and continuous improvement., • Grow your impact through leadership strategy and data-driven decision-making in a vital area of clinical development. Join us and help make CSL the partner of choice - for sites for investigators and for patients everywhere. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

Join Us as a Clinical Trial Manager Were seeking aClinical Trial Managerto drive the clinical delivery of research trials with precision and purpose. The role will oversee trials in the UK Ireland and the Nordics. If you thrive in a fast-paced collaborative environment and have a passion for clinical excellence - this role is for you! Location Requirement This role requires working inthe client Uxbridge office 50% of the time. Key Responsibilities • Leads local study team and acts as the main point of contact for the Northern European Cluster with the global study team, • Responsible for study oversight and delivery management (time budget quality) at country level from start-up to closure., • Develops country level patient recruitment strategy & risk mitigation, • Leads problem solving and resolution efforts including management of risk contingencies issue resolution and escalation to the appropriate stakeholder/s, • Manages trial budgets and vendor coordination, • Ensure inspection readiness of assigned trials within country. What You Bring • Minimum4-5 years of experiencein Clinical Research., • Strong background inClinical Trial Operations; experience in leading and participating as an active member of cross functional teams, • PriorCRA experience in the UK(preferred)., • PriorStart Up experience in the UK(preferred)., • Strong organization and time management skills and ability to effectively manage multiple competing priorities, • Excellent leadership communication and independent decision-making ability., • Familiarity withICH-GCPand global regulatory standards. Qualifications • Minimum - Degree in life sciences or allied health (or equivalent experience)., • Fluent in English both written and verbal. Learn more about our ___

The purpose of Medical Affairs is to provide and gather scientific insights to/from internal and external stakeholders and generate data that translates into clear compelling and strategic scientific exchange and medical education programs. These will impact recommendations guidelines and medical practice in order to have a positive impact on health. The Medical Manager (MM) is responsible for scientific exchange providing medical & scientific information medical education as well as medical insight generation for the influenza and respiratory vaccine landscape as well as Seqirus late-stage portfolio of vaccines. The region of responsibility will focus primarily on the UK and Republic of Ireland. The MM will support the Brand strategy in developing and executing the medical parts of strategy. The role interfaces with other functions within Medical Affairs and across the organisation in Commercial Regulatory Policy Government Affairs Market Access and other cross functional teams to ensure collaborative connectivity and a focused medical approach to supporting country and regional business objectives. The MM will contribute to the implementation of objectives by supporting development and execution of the tactics related to the medical strategy for one or more products within the portfolio. The MM will work collaboratively with the commercial team on material and activities development and will conduct review of materials and activities to ensure they are Code compliant. The MM will perform other delegated tasks within the area of Medical Affairs in line with the companys vision and strategic imperatives including ad hoc projects. This role requires a high ability to understand interpret and clearly communicate clinical and scientific data and information and maintain a high level of collaboration with medical and commercial operations functions. All activities should be in line with Seqirus UK and Republic of Ireland medical strategic objectives at all times and ensure to act in compliance and respect of all national laws and regulations and Seqirus compliance standards. This role aims to build credible and durable relationships with health care professionals (in particular key opinion leaders) and other relevant external stakeholders. The role requires a high degree of proactivity both within Medical Affairs and the broader organisation demonstrated by actively contributing to medical activities within projects and cross-functional teams in the delivery of process improvements and brand associated projects. Flexibility in the role is expected to support the broader cross-functional objectives which may change where needed. Responsibilities include: - External facing • Communicate new and other important approved medical content to targeted Health Care Professionals (HCPs) in local regional or national capacities including Vaccines HCP decision-makers national and regional Key Opinion Leaders (KOLs) national and regional professional associations JCVI government organizations primary care key stakeholders at regional level and any other HCP who may be considered an influencer for flu protection., • Provide externally truthful accurate and scientifically supported information in response to unsolicited medical requests from HCPs and other stakeholders in a manner that complies with all applicable ethical governmental and Seqirus guidelines policies and procedures (e.g. medical inquiries scientific congress participation etc.)., • Provide internal product and indication expertise to any Seqirus/CSL colleague (e.g. field force training develop and update medical slides medical review and copy clearance etc.)., • Deliver presentations to relevant stakeholders in accordance with the designated medical strategy established by the country EMEA and Global Medical Affairs team., • Facilitate communication between HCPs and Health Care Organizations (HCOs) any healthcare decision maker and Medical Affairs colleagues., • Facilitate both Seqirus sponsored clinical trials collaborative research and investigator-initiated research activities as determined by Medical Affairs and in accordance with Seqirus SOPs (Seqirus sponsored research site/investigator interactions IIR inquiries etc.)., • Facilitate and support Medical Affairs contribution to awareness and education of all stakeholders in close collaboration with internal functions., • Search actively for customer insights that contribute to the development of product medical strategies and provide these to Seqirus as appropriate. Internal facing and Cross-Functional Collaboration • Work closely in the local medical team to ensure generated insights are captured shared and escalated as needed., • Provide internal product and indication expertise for any Seqirus/CSL colleague (e.g. field force training develop and update medical slides medical review and copy clearance etc.)., • Engage and collaborate with Marketing Market access Policy Sales Team Customer Services Communications at a local level and Medical Affairs teams at regional EMEA and when necessary at a global level., • Develop and maintain in-depth medical science expertise for designated disease area and products including analysis of current literature opinion and recommendations., • Be a proactive and strategic member of designated brand/business cross-functional teams., • Work with marketing and other relevant staff to contribute to brand strategies and supporting materials for designated products in local and global markets (as required)., • Be a proactive and strategic Member of designated brand/business cross-functional teams., • Provision of medical and clinical support to brand team in product launches issues management competitor complaints and recall situations., • Provision of expertise to submissions and presentations to local and global government authorities where relevant to achieve recommendations of Seqirus products., • Contribute to development and execution of medical plan departmental and cross-functional projects issues management, • Initiate and/or lead designated departmental and functional and/or cross functional projects., • Identify issues and collaborate with relevant stakeholders to resolve., • Manage the review and approval process for funding of study research proposals from external investigators as required., • Ensure compliance with all internal and external policies procedures and regulations e.g. Code of Practice financial processes, • Participate to all compliance training in line with timelines and Code of Practice requirements, • Contribute to internal signatory/approval process, • This role reports to the Medical Director UK and Ireland., • Maintain close coordination with medical counterparts to ensure activities are aligned with overall medical priorities as described in medical operating plans strategies initiatives and projects as appropriate., • Maintain close collaboration with the medical and commercial operations organization including marketing market access sales and customer services and other interacting Seqirus functions., • Actively drive support engage and contribute to external meetings (e.g. with HCP such as F2F or Advisory Boards) as well as internal meetings., • Drive plan and execute medical education programs and initiatives in the influenza travel or other vaccine landscape., • Contribute to the medical planning for asset/asset team projects and activities and work with medical leadership to develop and implement the Field Medical team medical plan for Seqirus products., • Serve as a project lead and/or support for assigned Medical Affairs projects. Contribute to development and execution of key projects. Qualifications Skills and Experience: - • A Master in Biological Science Medical or Clinical discipline or Pharmacy with complementary experience in the pharmaceutical/ biotechnology/ healthcare industry preferably in vaccines; PhD in relevant field or MD preferred, • Experience in clinical and/or health services education or research (preferably in the pharmaceutical industry)., • Experience with clinical research and/or pharmaceutical industry as MSL Medical Advisor or other relevant position, • Experience in influenza infectious diseases epidemiology vaccines public health and the health care system, • Holds a driving license, • Willing to travel across UK and Republic of Ireland and internationally according to business needs, • Required to be flexible in working hours CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. 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Worth Recruiting Property Industry Recruitment Job Title: LETTINGS MANAGER / LISTER Residential Lettings Location: West Drayton UB7 Salary: 50000 per annum Position: Permanent Full-Time Reference: WR65143 A highly regarded Estate & Lettings Agency is seeking an experienced and ambitious Lettings Manager / Lister to oversee their operations in the West Drayton and Ruislip area. This role involves generating new business securing instructions managing a proven lettings team and ensuring excellent customer service. The ideal candidate will combine strong leadership and mentoring skills with a proven record of valuing and converting instructions. What Youll Be Doing (Key Responsibilities): • Leading and managing the lettings office and team, • Carrying out valuations and securing new instructions, • Driving business growth and market share in the local area, • Mentoring motivating and developing staff performance, • Overseeing day-to-day lettings operations and compliance, • Delivering exceptional customer service to landlords and tenants, • Building strong local presence and community connections, • Significant estate agency and lettings experience (essential), • Proven track record in listing and winning business, • Experience managing and motivating a lettings team, • Excellent sales conversion skills, • Strong communication and interpersonal abilities, • Highly organised ambitious and proactive, • Professional articulate and well-presented, • Exceptional customer service skills, • Competitive salary & OTE, • Generous basic salary plus commission, • Career progression within a respected local firm, • Supportive dynamic team environment, • Five-day working week If you are interested in this Lettings Manager / Lister role please contact the Property Recruitment Team at Worth Recruiting today quoting reference: WR65143. About Your Application: • Response Time: We receive a great many applications and respond as quickly as possible. If you have not heard from us within 48 working hours please assume that on this occasion your application has not been successful., • Data Protection: Worth Recruiting is acting as a recruitment agency in relation to this position. By submitting your application you consent to Worth Recruiting processing and storing your data for the purposes of your job search. For more information please see our privacy policy on our website., • Confidentiality: All communications with Worth Recruiting are completely confidential. We will always need to speak with you before we are able to submit your CV to our client. Job Reference: WR65143 Lettings Manager / Lister Required Experience: Manager Key Skills Google Analytics,Access Control System,Clinical Research,Graphics Design,CSS,Documentation Employment Type : Full-Time Experience: years Vacancy: 1 Yearly Salary Salary: 25000 - 50000

Fortrea 2026 University Internship Program Clinical Costing Department Location: UK remote Full-time 12-month Start Date: July 2026 KICKSTART YOUR CAREER IN LIFE SCIENCES At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internshipits a launchpad for your future. As an Internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll work on meaningful projects learn from experienced professionals and see firsthand how clinical research and healthcare innovation change lives. We dont expect you to know it all. What matters most is your potential your drive to learn and your willingness to grow. With hands-on experience mentorship and structured development well help you build the skills and confidence to succeed. Your journey to pioneering tomorrows breakthroughs starts here. About the Team: The Clinical Costing Team is part of the Enterprise Client Solutions function and is responsible for developing the clinical monitoring and resourcing strategy for all late-stage request for proposals from our clients. This team is responsible for ensuring that the budget solutions we provide to our clients are not only competitive but also operationally sound and feasible. Internship Assignment Summary: • Attend training sessions to learn the drug development process and how clinical research is planned conducted and reported., • Familiarize yourself with the various tools and processes that the clinical costing team utilizes to develop the budgets for clinical studies., • Support the team with special projects and analytics which get an opportunity to present to senior management for more informed decision making., • Engage and learn with the senior team members by shadowing them in their daily activities and learn the strategy behind the operations of clinical research to enhance your knowledge and skills into this exciting domain. Education/Qualifications/Skills: • Working towards bachelors or masters degree in life sciences bio-medical pharmacy nursing medicine STEM or equivalent., • Candidates should still be students enrolled into placement in their 2nd year taking a gap year for a 12 months internship as part of their Bachelors degrees., • Has experience delivering projects in an academic setting., • Ability to collaborate and communicate well with various stakeholders and internal/external colleagues., • Embraces diverse and innovative ways of thinking through various forms of collaboration and partnership., • Good analytical and informatics technology/ computing skills To ensure a strong application we kindly ask that you submit your CV along with a cover letter detailing your motivations for pursuing a Costing internship with our team. Physical Demands/Work Environment: Work Environment: * * Work is performed in an office environment with exposure to electrical office equipment. * Occasional drives to site locations with occasional travel both domestic and international. Physical Requirements: * * Frequently stationary for 6-8 hours per day. * Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists. * Occasional crouching stooping with frequent bending and twisting of upper body and neck. * Ability to access and use a variety of computer software developed both in-house and off-the-shelf. * Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. * Regular and consistent attendance. * Varied hours may be required. Learn more about our ___

As the CSL Seqirus Head of Medical Affairs UK and Ireland you will report into the Regional Head of Medical Affairs EMEA; leading a team of highly talented team medical affairs colleagues that have both scientific and clinical expertise. You will lead the team to successfully execute all critical medical affairs functions which include developing and executing the strategic medical plans for UK and Ireland managing key thought-leader relationships publishing data from corporate-sponsored trials disseminating/presenting educational information on the portfolio answering questions from healthcare clinicians and disease experts regarding product safety or efficacy that is not addressed in a products label and supporting research initiatives outside labelled indications for marketed products. You will collaborate with the Regional Medical Head in developing medical strategy and ensuring consistency of approach and deliverables for UK and Ireland Medical Affairs activities. Responsibilities include: • Ensure CSL Seqirus Influenza and other respiratory viruses portfolios medical plans are successfully developed and executed to achieve short-and long-term objectives and support CSL Seqirus. Partners with commercial heads and ensures alignment on key strategies deliverables & communication. Serves as Influenza and other vaccines champion/expert effectively negotiating with & influencing key internal & external stakeholders. Develop and lead a committed and innovative UK and Ireland Influenza and other vaccines Medical Affairs Team with the following objectives:, • Provide quality and strategic medical input to achieve successful medical objectives for CSL Seqirus Influenza and other vaccines in UK and Ireland, • Engage with external experts research partners public health and government stakeholders to promulgate CSL Seqirus scientific platform and enhance company reputation, • Provide medical governance into decision-making and issue management and external communications, • Ensure local pharmacovigilance compliance, • Provide medical leadership for CSL Seqirus Vaccine Portfolio, • External Network Development & Management, • Identify key opinion leaders in infectious disease and cultivate a network of influenza experts within a given geography/nationally for key areas of scope vaccinology and antiviral therapies. Create an environment which serves to establish the medical team as the conduit for credible accurate and updated scientific and medical information between KOLs other investigators and CSL Seqirus internal functions, • Maintain excellent professional relationships with medical and public health experts government officials immunisation advisory committees such as JCVI partner companies. Accountable for engaging and cultivating relationships with leading KOLs to gain contribution/ participation in advisory boards greater understanding of influenza vaccines and insights into unmet patient needs, • Represents CSL Seqirus at scientific and medical forums including medical education forums scientific roundtables congresses and symposia, • Planning designing and managing or participating in local regional national and global medical Advisory Boards including working with vendor(, • s) in support of medical affairs strategies Strategy & Scientific Expertise • Develop and Design the UK and Ireland medical strategic plans for Influenza and other vaccines and works closely with the Regional Head of Medical Affairs to ensure the implementation of the Med. Affairs strategy plan, • Provides medical leadership for scientific communications including core scientific statements standard responses Phase IV plans medical symposia medical education activities and publications, • Provide medical input and advice into development of commercial campaigns where applicable and ensure that timely support and accuracy for Medical Copy Clearance is accomplished for all CSL Seqirus vaccines in UK and Ireland, • Scientific Oversight of UK and Ireland Phase 4 studies: work with external experts and cross functional team to ensure Phase 4 studies for the region are completed to agreed timelines and budget., • Serve as authoritative source of clinical expertise on CSL Seqirus vaccines including primary responsibility for interaction with regulatory agencies for clinical product maintenance activities. People Management • Manage and develop field and office based medical team within the Influenza and other vaccines therapeutic area and/or geography including hiring training evaluation and motivation in alignment with CSL Seqirus corporate values medical strategies and objectives. Provide strong leadership to motivate the team and achieve outstanding results that align with department goals., • As a member of the Regional Medical Affairs leadership team work together to ensure consistency and compliance in medical decision-making and systems and processes for CSL Seqirus, • Implement and oversee compliant medical processes sign off promotional materials and management of Investigator-initiated clinical studies for UK and Ireland., • Develop monitor and accountable for the UK and Ireland Influenza and other vaccines Medical Affairs budget Qualifications Skills and experience: - • A degree in the Sciences such as a MD; PhD; PharmD; DrPH; or DSc, • Minimum 7-10 years experience in Pharmaceutical industry, • Experience in driving the medical strategy of products with excellent working knowledge of regulatory affairs pharmacovigilance research and clinical development programs, • Extensive experience with industry promotional codes and procedures, • Knowledge and understanding of drug development processes with specific expertise on vaccines, • Superior technical medical knowledge regarding influenza vaccines and pandemic vaccines, • Strong ability to critically review business plans and make recommendations, • Advanced scientific and/o medical degree with relevant or related experience preferably in vaccinology infectious disease epidemiology vaccine clinical development and medical affairs., • At least 10 years of experience in medical affairs scientific activities, • Ability to interact with KOLs and Government officials dealing with immunization programs/vaccine policy and vaccine recommendations at the highest levels., • Demonstrated experience in leading a matrixed team., • Demonstrated ability to lead across diverse cultures and geographies., • Significant cross-functional leadership/management experience. Demonstrated excellence in leadership behaviour., • Knowledge of immunization programs and an established network of KOLs within the vaccine field and relationships with established academic institutions, • Knowledge of the commercial and environmental issues that drive development vaccine projects., • Demonstrated ability in the design initiation and reporting of clinical studies as part of an integrated clinical plan., • Proven ability to influence and succeed through others and to form excellent relationships with key cross-functional stakeholders., • Documented ability to take a relevant vaccine or vaccine-preventable disease project from start to end including conception design protocol analytic plan implementation analysis and reporting and interpretation of results., • Able to review evaluate interpret and present complex data; understand the emerging safety and efficacy profile of CSL Seqirus Influenza vaccines, • Understand the critical data elements related to assessing the public health value of Influenza vaccines ability to oversee or conduct public health analyses of Influenza vaccine impact and ability to interpret data and data limitations for both CSL Seqirus and competitor Influenza vaccines., • Excellent verbal and written communication skills including scientific writing skills, • Proven ability to influence and succeed through others and to form excellent relationships with key cross-functional stakeholders., • Demonstrated strong work ethic and proven track record of delivering high quality within timelines., • Values and behaviours consistent with CSL Seqirus, • Ability to coach develop and direct those that report to Director of Medical Affairs CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. 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At AbbVie we turn science into medicine to improve patients lives. This role plays a key part in advancing our clinical pipeline by leading high-performing study start-up teams and fostering impactful partnerships with investigative sites. The successful candidate will drive operational excellence team development and strategic collaboration to position AbbVie as a preferred partner in clinical trials. Key Responsibilities Team Leadership & Development • Lead mentor and support a team of clinical research professionals focused on study startup activities., • Oversee hiring performance management coaching and career development., • Foster an inclusive and empowering team culture that encourages growth and accountability., • Ensure timely high-quality and budget-compliant delivery of assigned clinical studies., • Support ethics submissions accompanied site visits and audit readiness., • Monitor compliance with GCP ICH guidelines AbbVie SOPs and local regulations., • Build strong relationships with internal stakeholders (e.g. Medical Affairs affiliate teams) and external partners (e.g. KOLs investigators)., • Promote AbbVies reputation through coordinated and impactful site engagement., • Use AbbVie tools and systems to proactively manage performance metrics risks and resources., • Conduct gap analyses and trend assessments to identify training needs and drive continuous improvement., • Manage resource allocation in line with portfolio priorities., • Participate in global/local initiatives to streamline processes and enhance delivery. Qualifications : • Bachelors degree or equivalent in a health-related field (e.g. Medicine Pharmacy Nursing Life Sciences), • Minimum 3 years of clinical monitoring experience, • Strong interpersonal and cross-functional communication skills, • Experience in motivating and mentoring others with a growing capacity to lead teams effectively. Has the ability to provide transparent and timely feedback to raise the bar on individual and team performance., • Strategic mindset with solid planning and organizational skills, • Comfortable navigating ambiguity and making timely data-driven decisions, • Experience across multiple therapeutic areas and study phases is a plus, • High integrity and alignment with AbbVies leadership values, • Self-driven adaptable and proactive Additional Information : AbbVie Culture At AbbVie we care deeply about bringing innovative solutions to patients in need. By joining us as a Product Specialist youll be at the forefront of our mission working in a dynamic and supportive environment that encourages growth and collaboration. • All4OneAbbVie: Foster strong interpersonal relationships and teamwork., • Decide Smart & Sure: Navigate ambiguity and make informed decisions., • Agile & Accountable: Communicate a clear and inspiring vision., • Clear & Courageous: Provide honest and constructive feedback. US & Puerto Rico only - to learn more visit ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary The Senior Manager R&D Data Stewardshipprovides operational support for data stewardship initiatives by helping manage data standards track data quality and assist with stewardship tooling and documentation. Works closely with data stewards IT and scientific teams to support consistent and compliant data practices. Main Responsibilities: * Define and maintain data dictionaries metadata standards and data management workflows. * Manage data curation and wrangling activities to deliver accurate standardized and metadata enriched data for downstream scientific/data science analytics or integration into data platforms. * Support data quality monitoring activities & resolution of data issues discrepancies and prevent duplication or corruption * Support remediation activities and root cause analysis; track issues to ensure timely implementation of corrective and preventive actions. * Lead process improvement initiatives by identifying opportunities for enhanced quality or efficiency. * Engage with external stakeholders and partners to ensure data quality compliance with standards and adherence to contracts & data-sharing agreements. * Coordinate stewardship-related communications documentations training and change management activities. * Support data stewardship teams in onboarding and effective use of data management tools (e.g. central data repositories metadata catalogues data management platforms/portals). * Work with IT and platform teams to validate integration of data management processes into systems. Qualification: * Bachelors degree in Life Sciences Information Sciences or related field. * 7 years of experience biomedical R&D data management or related roles. * Experience managing data across Research Clinical Safety and/or Regulatory domains. * Knowledge of FAIR data principles and regulatory requirements. * Familiarity with data quality concepts and metadata management and governance principles. * Experience working with data and scientific platforms in a collaborative environment. * Detailed oriented with strong documentation and communication skills. We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Associate Director Global Feasibility Lead is responsible for leading the strategic planning and execution of global feasibility assessments across clinical development programs. This role ensures that feasibility activities are data-driven regionally informed and aligned with the broader clinical and operational strategy. Operating within a matrixed and cross-functional environment the Associate Director partners with therapeutic area leads clinical operations and external service providers to deliver robust feasibility insights that inform country and site selection enrollment forecasting and risk mitigation strategies. The role also oversees the development and deployment of feasibility tools manages feasibility data integrity and ensures timely delivery of feasibility outputs to support protocol finalization and study startup. This position plays a critical role in early engagement with investigators and sites shaping the feasibility narrative and contributing to the operational design of clinical trials. The Associate Director is expected to proactively identify feasibility risks propose mitigation strategies and escalate issues as needed to ensure successful trial execution. Main Responsibilities and Accountabilities • Feasibility Strategy Development: Lead the design and implementation of global feasibility strategies to support protocol optimization and country/site selection., • Cross-Functional Collaboration: Partner with clinical operations therapeutic area leads and external vendors to gather input and align feasibility outputs with study needs., • Data Analysis & Forecasting: Analyze historical data epidemiology and site performance metrics to generate enrollment forecasts and identify potential risks., • Feasibility Tool Management: Oversee the development and deployment of feasibility tools and templates to ensure consistency and quality across programs., • Stakeholder Engagement: Facilitate early engagement with investigators and sites to validate feasibility assumptions and support study startup planning., • Act as the primary point of contact both internally and externally (e.g. vendors) as applicable for anything study related., • Maintain up to date knowledge of the therapeutic area/product candidate(s) clinical practice competitors and regulatory considerations., • Support audits/inspections and resolutions of findings., • Support in the development of new SOPs guidelines etc and/ or participate in working groups about new processes., • Functional leadership and mentorship of junior staff required; Act in advisory capacity to other clinops colleagues within and across TAs., • When accountable to a set of studies and/or program (s) provides oversight and direction ensuring appropriate delegation and delivery inter-program efficiencies and applied learnings. Job Qualifications and Experience Requirements Education At minimum bachelors degree or equivalent in life science nursing pharmacy medical laboratory technology or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g. diploma or associate degree RN certified medical technologist). Experience • As a guide a minimum of 10 years relevant clinical research (or related) experience within the pharmaceutical industry., • A solid understanding of the drug development process and specifically each step within the clinical trial process., • Experience in running feasibility activities for large and/or complex global clinical trials., • Robust budget forecasting and management experience., • Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Competencies • Demonstrated ability to lead teams and work in a fast-paced team environment., • Experienced in working within a Matrix Environment and ability to work through interpersonal difficulties and resolve conflicts with a Matrix Environment, • Successfully demonstrated the ability to mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities., • Ability to evaluate judge and make decisions regarding staff. Ability to teach/coaching and setting an example of best practice., • Excellent interpersonal and decision-making skills., • Demonstrates innovation. Possesses drive energy and enthusiasm to deliver the program objectives., • Skilled at independently navigating new or novel indications study/program approaches and unique challenges., • Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report., • Ability to plan and ensure execution and completion of clinical program(s) to the highest ethical and scientific standards., • Extensive and comprehensive knowledge of ICH guidelines/ GCP Maintains current medical/scientific/regulatory knowledge., • Demonstrated project management skills including simultaneous management of multiple projects. Possesses excellent planning time management & coordination skills. We encourage you to make your well-being a priority. Its important and so are you. 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Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas including Hematology/Oncology and Ophthalmology. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a supportive fast-paced and innovative global CRO. National monitoring across the UK Oncology focus including solid tumor studies Prostate NSCLC Leukemia Breast Glioblastoma & Hematological Malignancies Exposure to multiple protocols across Neuroscience Cell/Gene Therapies Respiratory Cardiovascular Infectious Disease Nephrology Endocrinology & Gastroenterology Risk-based monitoring model for smarter trial management 8 on-site days per month At our global CRO we blend 30 years of expertise with innovation offering: Personalized development plans & career progression A supportive environment with flexible Line Managers Exciting collaborations with biotech & biopharma pioneers Make a real impact in clinical research while building your career with a company that invests in your growth and success! Ready to make a difference Lets connect! Learn more about our ___

CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. TheHead of Clinical Compliance and Specialty Operationsis a senior leadership role responsible for ensuring that clinical development activities are conducted in full compliance with global regulatory requirements internal policies and Good Clinical Practice (GCP) standards. This role also provides strategic and operational oversight for specialized clinical operations functions including clinical lab sample management TMF operations and the execution of studies via full-service outsourcing (FSO) models. Clinical Compliance Leadership * Lead the development implementation and continuous improvement of the clinical compliance framework across all therapeutic areas. * Serve as the primary point of contact for inspection readiness and regulatory audits. * Partner with Quality Assurance and Clinical Operations to identify assess and mitigate compliance risks. * Ensure harmonization of compliance practices across global teams and integration of acquired entities or business units. Oversight of Specialty Operations * Trial Master File (TMF):Oversee the TMF team to ensure timely accurate and inspection-ready documentation in alignment with ICH-GCP and internal SOPs. * Clinical Lab Sample Management:Provide strategic direction and operational oversight for the Center of Excellence (CoE) in lab sample management ensuring robust interfaces with research and clinical teams. * Full-Service Outsourcing (FSO):Provide strategic direction and ensure operational infrastructure is developed and implemented for FSO delivery models. Strategic Operations & Governance * Collaborate with the Head of Clinical Operations and other functional leaders to shape the future-state operating model including phased implementation plans (e.g. Day 1 Month 3 etc.). * Support the development of operational KPIs and dashboards to monitor compliance and operations performance. Qualifications & Experience Requirements * Degree (BSc/MSc/Diploma) in scientific/medical/pharmaceutical discipline is essential preferably combined with relevant clinical trial experience * Extensive understanding of the clinical research and drug development lifecycle * 10 years of professional work experience in a Clinical Development/Research environment * Thorough knowledge of ICH GCP FDA GCP Regulations and EU clinical trials directives * Ability to lead and influence programs of change across many groups not in the direct line of supervision * Proven leadership and global Clinical Operations experience is essential * Proven track record in leading global teams We encourage you to make your well-being a priority. Its important and so are you. Learn more about ___

The role Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is to be office based in central London for at least 3 days a week with the rest of the time being spent working from home. Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK. Much of the work will involve complex oncological clinical trials providing valuable opportunities to develop your skills and expertise. What Youll Do: Communicate with project teams and track study activities Maintain essential documentation and regulatory compliance Support site and study material preparation Assist with meeting coordination minute-taking and documentation Manage Trial Master File (TMF) documentation and quality control Liaise with vendors and coordinate study supply shipments Provide general administrative and systems support Requirements: • A minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - this is essential!, • Must be within commuting distance of Central London (office-based 3 days per week), • Basic understanding of biology and biological processes, • Good organizational and time management skills This role is a full time & permanent position to be employed through Fortrea. This is a great opportunity to gain hands-on experience in clinical research and contribute to high-quality clinical data production. If you thrive in a fast-paced environment and enjoy working with a dynamic team wed love to hear from you! Learn more about our ___

• Align with the Director to enhance the roadmap and develop the action plan to implement AbbVies Patient Inclusion strategy across the portfolio, • Collaborate with cross-functional partners to identify process improvements to disease area strategies and clinical trial lifecycle to increase representative patient participation, • Partner with regionally aligned counterparts in Patient Inclusion to develop a strategy to scale current patient inclusion framework to indication level plans that incorporate global considerations, • Identify relevant data sources that synthesize clinical epidemiological and real-world evidence on disease prevalence incidence burden and health disparities and extract meaningful data to support global patient access strategies., • Work in-region to support global expansion of Patient Inclusion capabilities and processes, • Influence leaders to champion internal behaviors to strengthen our understanding of disease disparities and the effects of representative populations, • Work with key stakeholders to develop TA/indication level strategies to increase representation in clinical trials, • Maximize external engagement by leveraging existing relationships and exploring new opportunities to collaborate with community partners patient advocate organizations institutions and key Health Care Practitioners to broaden knowledge about clinical research in underrepresented communities and support the patient care journey., • Reinforce alignment between the Patient Inclusion principles and AbbVies business strategy, • Monitor impact of Patient Inclusion strategies based on analytics to demonstrate improvement in trial representation Qualifications : • Bachelors Degree in a scientific field required Advanced degree is desirable., • Minimum of 8 years of pharma-related/clinical research experience or equivalent, • 6 years of patient recruitment project management and people management (preferred), • Advanced working knowledge of ICH and GCP guidelines required., • Operational understanding of the global regulatory environment is desirable., • Strong proficiency in authoring and reviewing scientific medical and regulatory documents to ensure consistency and strategic alignment with global submissions, • Skilled in managing the end-to-end development of regulatory-ready submission documents, • Excellent collaborator and articulate communicator easily builds relationships across geographic locations and gains cross functional alignment., • Strategic thinker with understanding of clinical development process and uses data to drive the business and continuous improvements. Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

Location: London (Hybrid) - 23 days/week on-site Were looking for an experienced Clinical Research Manager to lead country-level clinical trial operations. Youll ensure performance quality and compliance across assigned protocols manage vendors and sites and collaborate with internal teams (PV Regulatory GMA GHH). This is a customer-facing role with significant impact on trial delivery and country commitments. Key Responsibilities: • Oversee protocol execution timelines and budgets, • Ensure compliance with ICH-GCP and local regulations, • Lead quality oversight and training for CRAs/CTCs, • Build strong relationships with investigators and vendors, • Contribute to local and regional strategy Requirements: • 68 years clinical research experience (pharma/CRO/healthcare), • Strong knowledge of ICH-GCP and drug development, • Excellent communication and leadership skills, • Ability to manage multiple protocols and stakeholders, • London-based on-site 23 days/week Apply now and make an impact on the future of clinical development! Learn more about our ___

Role overview: The Medical Science Liaison (MSL) will provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts. This role will ensure a strong medical and scientific presence for AbbVie by facilitation of research and educational initiatives while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie. The MSL will also partner with Clinical Operations to assist in the initiation and oversight of clinical studies. Key Responsibilities: • Develop and maintain high level of knowledge regarding therapy area and AbbVie products including awareness of the competitive landscape, • Deliver presentations on clinical and scientific topics ensuring compliance approval., • Organise and participate in external education and training events as appropriate., • Facilitate and support AbbVies clinical trial programs., • Facilitate and support publication of clinical data in line with AbbVie Strategy., • Facilitate other research activities e.g. collection of real-world evidence and development of Investigator Study Proposals in line with AbbVie Strategy., • Identify collect and internally provide insights into medical and scientific field intelligence such as competitor research medical strategies educational activities, • Identify and develop new KOLs in line with AbbVie strategy., • Develop KOL advocacy through provision of scientific and clinical information and involvement in appropriate medical affairs activities., • Organise and deliver advisory board meetings and round-table-meetings with appropriate HCPs to gather business-relevant information and stimulate scientific exchange with HCPs., • Attend appropriate scientific congresses to interact with KOLs and develop knowledge regarding the wider therapy area and competitor information., • Contribute to scientific dossiers and reports where appropriate., • Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives, • Provide guidance regarding appropriate speakers for national/international congresses and workshops in order to spread and enhance scientific exchange., • Support the business unit by attending and contributing to national leadership meetings and working cross-functionally., • Organise clinical and scientific education as well as in-house training for sales reps and other appropriate staff as required. Qualifications : Advanced degree (e.g. PharmD. MD PhD) in a relevant scientific discipline is preferred an undergraduate degree in a relevant discipline with demonstrated experience will also be considered. • Experience in Medical Affairs within a Pharmaceutical company and/or experience working within Neuroscience is highly preferred, • Experience in developing and maintaining expert knowledge for the assigned therapeutic area and in medical research in general., • Ability to comprehensively learn about new subject areas and environments., • Excellent written and spoken communication and presentation skills with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders physicians and other healthcare decision makers., • Strong commitment to compliance with the relevant rules and procedures and to scientific quality and integrity. Additional Information : AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more visit ___

Are you looking to grow your career in clinical research Fortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs. • Be part of a global innovative organization driving advancements in clinical research., • Work on cutting-edge trials across a range of therapeutic areas., • Enjoy flexible career progression with opportunities at different CRA levels., • Benefit from a collaborative team environment that values mentorship and growth., • Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements., • Manage all aspects of site activities including site initiation monitoring visits and closeouts., • Ensure patient safety data integrity and adherence to GCP guidelines., • Support feasibility assessments investigator recruitment and vendor coordination., • Mentor junior team members and contribute to quality control efforts., • Track and report Serious Adverse Events (SAEs) as required., • Bachelors or Masters degree in Life Sciences or equivalent., • 3 years of relevant clinical research experience with at least 1 year of previous monitoring experience., • Ability to work independently and manage multiple priorities., • Basic knowledge of regulatory guidelines and the clinical trial process., • Strong communication organizational and problem-solving skills., • Valid drivers license and willingness to travel nationally (68 visits/month). Ready to take the next step in your CRA career Apply now and be part of groundbreaking clinical research at Fortrea! Learn more about our ___

Make a meaningful impact by shaping how CSL partners with clinical research sites worldwide.Find out if this opportunity is a good fit by reading all of the information that follows below.At CSL, were driven by a single purpose: to deliver innovative therapies that improve patients lives.The Site En

Now accepting applicants for Focus Group studies. Administrative Assistant Admin Work From Home - Part Time Remote Focus Group Panelists. Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments.

Administrative Assistant Admin Work From Home - Part Time Remote Focus Group Panelists. Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments. With most of our paid focus group studies, you have the opt

We at TFP are looking for brilliant minds and passionate hearts to help us shape the future of fertility. We are one of the largest fertility service providers in Europe operating our IVF clinics and egg/sperm freezing banks in the UK Poland and Netherlands. We have embarked on the mission to use technology to provide patients with a memorable best-in-class fertility journey that leads to the best outcome starting a family! At TFP we offer all our patients the care understanding and expertise that help to bring dreams to life. We are passionate about what we do which reflects our commitment to creating lives and changing lives. Science research and innovation are key to how we work and have led to us pioneering fertility treatment for more than 35 years. Many of our clinicians are internationally renowned specialists and we regularly share knowledge across our clinics to further improve our success. Join us at TFP Fertility where your passion and expertise can contribute to our legacy of excellence. The Role: The post-holder will work under the remit of the specialist nurses working within the clinic. Main duties are working with the nursing team to support patients on their fertility journey from assisting with initial investigations right through to being present at events following treatments. Other tasks includea wide range of administrative skills to book patients in for treatment generating treatment plans and ensuring all documentation is complete ensuring regulatory requirements are met. This role is also a very practical role requiring a dynamic individual who is competent to assist with procedures throughout that journey to include theatre running phlebotomy and many more tasks. This is a permanent part time position working 25 hours per week The Location: Thames Valley Fertility (TVF) was established in 2017 and due to the passion expertise and reputation of our team has already grown into a leading fertility clinic. Providing treatment to both NHS and private patients TVF performs approximately 550 fresh cycles and 450 frozen cycles per year. Offering a full suite of treatment and diagnostic services including PGT. Conveniently located on the outskirts of Maidenhead adjacent to junction 8/9 of the M4 there is ample free parking for staff and patients at the front of the building. Key Responsibilities: * You will be responsible and accountable for the delivery of high quality care to meet the needs of the patients * Under direction you will develop skills in the instruction advice and care of couples throughout their treatment process. This involves clinical theatre and recovery roles * Phlebotomy * Patient contact - in person on the telephone and via email * Complete patient and group paperwork on time and with accuracy * Assisting in theatre and recovery * Other duties as instructed by your line manager * Administration for management of patient treatment cycles and to assist nursing staff as required Qualifications and Experience: * Previous experience as a Health Care Assistant * IT literate * Interest in Womens Health * Good communication skills * Previous experience in Fertility Clinic or Outpatients department desirable * Phlebotomy skills desirable Location: TFP Thames Valley Fertility - Maidenhead Working Hours:25 Monday to Friday Weekend working required at approximately 1:4 Salary: Competitive (Depending on experience) Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days Bank holidays Your application has been successfully submitted!

A leading global biopharmaceutical company is seeking a Medical Science Liaison to provide scientific leadership and support educational initiatives. The ideal candidate will have an advanced degree and experience in Medical Affairs or neuroscience.

A compassionate, skilled nurse with advanced clinical and assessment expertise. Provide expert clinical assessment, management, and support for patients with lung cancer throughout their care pathway. Participate in clinical research and support recruitment where applicable.