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UK Intern - Medical Governance Associate. At Kyowa Kirin International (KKI), our purpose is to make people smile.

We are looking to recruit a Social Worker – Support and Safeguarding Team within the Children’s Social Care industry in Windsor & Maidenhead on a permanent basis paying £44,799-£48,932 P/Annum.

About Loveday Ensure all your application information is up to date and in order before applying for this opportunity. Loveday is the UKs leading provider of luxury senior living and care. We are proud to combine world-class hospitality with exceptional clinical expertise, creating residences that not only feel like five-star hotels but also deliver truly personalised support. xrnqpay Our residences in Kensington, Belgravia, Abbey Road and Esher are designed with elegance, comfort and dignity at their core. E... JBLK1_UKTJ

This is a great opportunity for aspiring psychologists, teachers or therapists.

To enable vulnerable people with mental health needs to maximise independent living skills and opport. We're looking for a kind, confident and compassionate Support Worker to join our Mental health Services in Slough.

Apply now to join our great team of Care Assistants.Care Outlook to help improve the lives of the vulnerable and elderly in our extra care schemein Slough SL1 3FT.As a healthcare assistant, you will be providing personal care, building relationships, and making a big difference to those who need it

Support Workers will provide support to customers to help them develop the life skills they require to meet the assessed needs of the customers of the service. These aren't token gestures - we've thought long and hard about how best to support our team. We're looking for 3 kind, compassionate and r

Aspiring Educational Psychologist role. Would you like to build your experience working with Complex Needs and work alongside trained therapists, counsellors and psychologists?. This is a FANTASTIC opportunity for the mental health assistant to work alongside the therapists and psychologists based o

We are looking to recruit a Social Worker – Support and Safeguarding Team within the Children’s Social Care industry in Windsor & Maidenhead on a permanent basis paying £44,799-£48,932 P/Annum Responsibilities include: Safeguard and promote the welfare of children in

No experience is required and full training will be provided on the Job to enable you to become a qualified Dental Nurse and registered with the GDC (General Dental Council). As a Trainee Dental Nurse you will be required to pay for your training programme with flexible interest free payment option

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!

RF Ref #: 272Date: 20 October 2025Are you looking for your next step in Optometry This is your chance to join a leading modern practice located in the heart of Windsor one of the UKs most desirable places to live and work. With incredible transport links a brand-new refit and an environment built around clinical excellence and professional development this opportunity offers the perfect mix of career growth lifestyle and stability.Whether you prefer a 4-day or 5-day week these roles offer flexibility with Saturdays preferred (Sundays already covered) a supportive team and access to the latest optical technology. Why This Opportunity Stands Out Up to 33 days annual leave recharge properly 30-minute direct train to London city access without the city stress GOC & College fees fully paid Recognised as a Great Place to Work enhanced sick pay parental leave & wellbeing benefits Generous eyecare & hearcare perks (220 glasses allowance free eye tests free OCT & more) Pension contribution Parking fees covered Free Nespresso all day Major store refit completed in November 2023 modern stylish and future-ready Option to work across two high-performing stores Clear pathway for clinical progression & professional accreditation Latest technology throughout including OCT phoropters & autorefractors Supportive friendly team culture with excellent admin and pre-test support About the Role • Part-time (4 days) and full-time (5 days) roles available, • Saturdays preferred Sundays fully covered, • Mix of private and NHS patients with longer appointment times available, • Opportunity to expand into enhanced services IP pre/post-op care and more, • Be part of a forward-thinking team where your clinical input is valued and supported Why Windsor, • A historic and vibrant town with royal heritage riverside walks boutique shopping and top-rated dining, • Perfect base for professionals seeking London access without London living

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 ___

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 ___

AQP (Appropriately Qualified Person) Signatory for the UK Affiliate in line with the ABPI Code of Practice. Supporting both compliant meeting arrangements approvals for both UK and overseas meetings and the approval of specific non promotional materials for the UK Affiliate in line with the Code of Practice. RESPONSIBILITIES: • Provide cross therapy area meetings approval support examining UK meetings and certifying overseas meetings and travel arrangements, • Provide materials approval support for materials examining in line with company quality standards and the Code, • Attend Brand Team Meetings to ensure meetings plans/agenda focuses are communicated and understood, • Attend ad-hoc brand team meetings functional Medical meetings for compliance with company approvals standards, • Advise commercial and medical team project owners on compliant meetings planning, • Support the continued implementation of a Code Compliant system for all promotional and non-promotional activities throughout AbbVie and the marketplace ensuring the company is in line with the Association of British Pharmaceutical Industry (ABPI) standards the MHRA blue guide for advertising and promotion and all applicable international Codes of Practice (EFPIA IFPMA and respective National Codes and National Regulatory Bodies) at all times., • Provision of workable compliant solutions to support business development opportunities/product launches and contribute to the development of marketing campaigns, • Independent timely accurate review and approval of materials in accordance with the relevant Codes of Practice., • Make appropriate evaluations when undertaking material reviews taking into account the risk profile in decision making, • Provide Guidance on UK Code requirements to Global/overseas affiliates and UK Affiliate as and when required, • Actively participate in cross-functional Medical Review Projects to build Medical Review standard practices and solutions to meet business needs, • Support evaluation of Materials exception reports and recommendations for corrective actions, • Adhere to the ABPI Code of Practice for the Pharmaceutical Industry in all aspects of work, • Confidently present PMCPA Code cases to encourage team learning To adhere to the ABPI Code of Practice for the Pharmaceutical Industry in all aspects of work. To be cognisant of and agree to adhere to Medical Division SOPs and Guidelines. To provide compliant solutions to meet business needs. Accountable directly to the Medical Review & Code Training Lead. GENERAL ACCOUNTABILITIES: To comply with the companys policies and procedures to meet statutory quality and business requirements within the overall strategy and objectives AbbVie Ltd. Qualifications : BACKGROUND/EDUCATION: • Life science degree essential, • 3 years of approvals experience with ABPI Code quality standards with up-to-date detailed knowledge of the Code, • Experience in understanding analysing and communicating complex pharmacy pharmacology and medical issues relating to a range of different therapeutic areas, • Experience in approving meetings in line with quality standards and the Code including Certification of overseas meetings, • Experience in reviewing non-promotional materials including corporate advertising press releases market research material, • Demonstrated experience in reference checking and copy approval 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 ___

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. Learn more about some of the ___

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. You will oversees all areas of single case processing in the global pharmacovigilance database from all sources. This includes ensuring that the vendor performs case processing in accordance with regulatory guidelines PV agreements and the Companys SOPs as well as responding to specific questions or queries about cases. This role develops standards and processes with a focus on global compliance and process optimization. Oversees Medical Evaluators responsible for medical review of ICSRs. Key Responsibilities Oversight of Case Management Processes activities Oversight of Medical Evaluator role which completes medical review of the following ICSRs: All serious cases from all sources Non-serious cases from company-sponsored clinical study if required Legal ICSRs (serious and non-serious) Reportable cases of combination products with device issue(s) / malfunction (serious and non-serious) Non-serious ICSRs are processed by Case Managers and reviewed for correct seriousness on an aggregate basis by Medical Evaluator Medical review includes: Review of seriousness listedness and causality assessments Review of event terms and MedDRA coding Review of narrative for medical accuracy and consistency Assessment of the need for Quality Investigations Generation of medical follow up queries / Targeted Questionnaires Drive department-wide planning: resource budget and org. strategy Own case management dashboards and governance scorecards Prepare for internal and external inspections including coordination of creation of presentations Lead transformation initiatives (e.g. vendor transitions digital tools) Monitor regulatory trends and represent PV case management in global initiatives Coordinate departmental leadership meetings and communication Pilot innovations (e.g. RPA AI triage tech integration) Align with Clinical QA Regulatory and Safety Science functions Coordinate creation and update of SOPs Retain product and process knowledge Skills and Education Required Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance (PV) experience with 5 years of managerial/leadership experience Global pharmacovigilance database knowledge is required along with proficient knowledge of global and local regulatory rules and regulations Qualifications and Education Required BS/BA RN Pharmacist or similar 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 ___

We are seeking a skilled and dedicated Social Worker to join the Duty & Assessment Team providing vital support to children young people and families across Windsor & Maidenhead. In this frontline role you will manage a diverse caseload involving Child Protection Child in Need and Looked After Children. You will conduct statutory assessments direct work with families undertake Section 47 enquiries and contribute to multi-agency safeguarding arrangements. This is a fast-paced and rewarding team where social workers are supported to deliver high-quality practice that protects children promotes positive outcomes and upholds their right to safety and wellbeing. • Undertake Child and Family Assessments in line with Section 17 and Section 47 requirements., • Visit children and families to assess risk strengths and protective factors., • Develop safety plans and implement interventions to safeguard children., • Lead and contribute to strategy discussions and multi-agency meetings., • Manage a caseload of CIN/CP/LAC cases ensuring timely progression and effective outcomes., • Prepare and present reports for statutory meetings including Initial Child Protection Conferences Core Groups and CIN meetings., • Support looked-after children through care planning and placement work., • Maintain detailed and accurate case records in line with local policy and statutory requirements., • Prepare high-quality court reports including Section 7 and Section 37 reports., • Present cases to Legal Panel and contribute to PLO processes., • Complete viability assessments family network assessments and applications for emergency/temporary orders., • Work collaboratively with schools health services police voluntary agencies and other safeguarding partners., • Participate in family network meetings and support joint-working arrangements., • Build strong relationships with children young people and carers., • Work in accordance with Social Work England standards and statutory guidance., • Participate in supervision development sessions and reflective practice opportunities., • Contribute to a culture of high-quality practice learning and improvement., • Social Work qualification (CQSW DipSW BA/MA Social Work or equivalent)., • Active Social Work England registration., • Evidence of continuing professional development., • Experience working with CIN/CP/LAC caseloads., • Strong ability to build effective relationships with children and families., • Confident in assessing risk and applying evidence-based decision making., • Experience preparing detailed reports for courts conferences and panels., • Knowledge of childrens safeguarding legislation and statutory frameworks., • Ability to manage complex caseloads and work under pressure., • Proficiency with ICT systems including case management tools., • Full driving licence and access to a vehicle for work purposes., • Compassionate resilient and child-centred approach., • Strong communication and negotiation skills., • Ability to work flexibly independently and with professional curiosity., • Commitment to positive outcomes for children and young people., • Enhanced DBS Check, • Proof of Right to Work in the UK, • Professional registration verification (Social Work England), • Satisfactory references, • Driving licence and vehicle access (for practice requirements), • Make a meaningful difference to children and families at critical points in their lives., • Join a supportive team committed to high-quality relationship-based practice., • Access ongoing training supervision and professional development opportunities.

Are you a qualified Dental Nurse looking for an exciting new opportunity Are you ready to step into a new challenge in a friendly and modern setting If so weve got a vacancy at our welcoming Windsor Centre for Advanced Dentistry in Windsor. • Full-time hours, • Typical shifts: 07:30 16:00 or 08:30 17:00 Monday to Friday (Early finish on Fridays), • Competitive hourly rate from: 14.50, • 5-surgery specialist private practice in specialist dentistry general dentistry aesthetic cosmetic restorative dentistry and implants, • Modern and well-equipped surgeries working alongside Specialists hygienists & therapists with a passion for learning and development. Wed love to receive your application to our Dental Nurse vacancy if you have the following skills and experience: • A recognised Dental Nursing qualification and active GDC registration, • A caring and empathetic approach with strong communication skills, • A team player who thrives on providing great service and building relationships with colleagues and patients In addition to a competitive salary our benefits package also includes: • Professional Fees Covered: GDC Indemnity and CPD costs fully covered, • Wellbeing Support: 24/7 Employee Assistance Programme offering confidential helpline and counselling services, • Health & Lifestyle Perks: Wellness hub with discounts on gym memberships online GP appointments and lifestyle coaching, • Smart Tech Benefits: Access to Techscheme spread the cost of the latest tech with convenient salary deductions PortmanDentex is a leading dental group where your skills and ambitions make a real difference. We support over 370 practices across the UK and Ireland. Were united by a shared commitment to exceptional dentistry patient-first care and helping each other thrive in work and beyond. Were united by a passion for great dentistry putting patients first and helping each other grow both at work and beyond. Application process When you click apply well just need your CV and contact details plus answers to a few quick questions and thats it! Youll hear back from us as soon as we can whatever the outcome. Ready to join us Click apply to take the next step in your Dental Nursing career. LI-ML1 IND001 Additional Information : We are an equal opportunity employer and value diversity equity and inclusion in our workplace. We are committed to creating an environment of mutual respect and are dedicated to providing equal employment opportunities regardless of race religion or belief sex sexual orientation gender reassignment pregnancy or maternity marital or civil partner status disability age or nationality. Remote Work : No Employment Type : Full-time Key Skills EMR Systems,Time Management,Dentrix,Organizational skills,Communication skills,Infection Control Training,Chairside Assisting,OSHA,Front Desk,Medical Imaging,Dental Assisting Experience: years Vacancy: 1

IP Optometrist Vacancy - Eye Academy Were proud to be an independent practice where patient care always comes first and joining us as our new Optometrist means being part of a team that values clinical freedom supports your development and encourages you to bring your personality and expertise to the role. We offer a welcoming people first environment across our different locations where your contributions are heard and your individuality is celebrated. Whether youre looking for the next step in your career or a fresh start in an independent group that genuinely puts patients and people before numbers this could be the right place for you. We offer a range of benefits designed to support your wellbeing development and work-life balance. Independent Prescribing Optometrist- Eye Academy Windsor An exciting opportunity has arisen for an Independent Prescribing (IP) Optometrist to join Eye Academy our luxury independent practice in the historic town of Windsor. At Eye Academy were known for blending premium eyewear collections with specialist clinical services. Across our award-winning practices we pride ourselves on offering patients the very best: from cutting edge diagnostics to luxury frames sourced from around the world. Our Windsor clinic also holds an NHS Ophthalmology Contract managing glaucoma and acute eye conditions making it the perfect setting for an Optometrist wanting to practise advanced care in a high-end environment. The Role • Provide expert care in glaucoma management and acute eye conditions under our NHS ophthalmology contract, • Conduct comprehensive eye examinations using state-of-the-art technology, • Independently manage and prescribe treatment plans as an IP Optometrist, • Independent Prescribing (IP) qualification (essential), • Diploma in Glaucoma (or working towards it) highly desirable, • Hospital Eye Service experience preferred, • Clinically driven with a passion for exceptional patient care, • Competitive salary and benefits package, • Ongoing support for further clinical development and professional qualifications, • A beautiful fully equipped practice with an experienced friendly team Windsor is a world-famous town steeped in history and home to Windsor Castle. Beyond the heritage its a vibrant hub of restaurants boutiques and green spaces by the River Thames. For commuters Windsor is well connected with direct trains to London Paddington and Waterloo (around 30 minutes) and easy access to the M4 M25 and Heathrow Airport. Its the ideal place to enjoy both professional growth and a fantastic lifestyle. If youre an IP Optometrist seeking the perfect combination of clinical challenge career development and luxury practice in a beautiful location wed love to hear from you. Click apply now and a member of our recruitment team will be in touch GBP 75000.00GBP 60000.00 Key Skills Children Activity,Criminal Justice,Customer Service,Accomodation,CAD,LTE Employment Type : Unclear Experience: years Vacancy: 1

Are you a Family Safeguarding Social Worker eager to join a team that truly values work-life balance and quality practice? Our client, a proactive local authority in South West England, is seeking dedicated social workers to make a meaningful impact on children's lives while enjoying a supportive an

Clinical Psychologist ADHD/ASD Assessments (London).

Join our award-winning team at Portman Dental and Implant Clinic a thriving 14-surgery practice renowned for its patient-focused care and clinical excellence. Were delighted to offer an exciting opportunity for a Dental Hygienist to become part of our friendly multi-disciplinary team. This position is initially offered as maternity cover with the potential for a permanent role for the right person someone who shares our commitment to exceptional dentistry and outstanding patient experiences. Youll be joining a talented team that includes a Specialist Orthodontist Specialist Endodontist Dentists with Special Interests in Periodontics and Cosmetic Restorative Dentistry Implant Specialists and Oral Surgery experts providing you with the perfect environment to grow and collaborate. Whats on offer: • Working: Monday Thursday Friday and every second Saturday, • Staring in January 2026, • Taking on a well-established and loyal patient base, • A supportive experienced and fully qualified clinical team What do you get in return By joining PortmanDentex youll be part of a 370 practice business which is predominantly focused on private dentistry. We are here to reimagine group dentistry and wellness using our scale and commitment to make this a reality. Our values of celebrating individuality aiming higher and growing together enable happier and healthier futures for all our clinicians colleagues and patients. Youll have access to our large network of like-minded clinicians as well as being surrounded by skilled practice teams wholl partner with you to deliver exceptional patient care. The support doesnt end there though we also offer: • Full clinical freedom meaning you can use your preferred equipment materials labs and referral pathways to deliver the best level of care to your patients. Well champion you as a self-employed clinician and ensure you always retain your unique identity, • Access to first class marketing branding and business support enabling you to maximise your diary utilisation, • Mentoring and CPD we can connect you with clinical mentors to guide and advise you as well as running regular CPD events with some of our best-in-class dentists and specialists #LI-SD1 Additional Information : We are an equal opportunity employer and value diversity equity and inclusion in our workplace. We are committed to creating an environment of mutual respect and are dedicated to providing equal employment opportunities regardless of race religion or belief sex sexual orientation gender reassignment pregnancy or maternity marital or civil partner status disability age or nationality. Remote Work : No Employment Type : Part-time Key Skills EMR Systems,Dentrix,Communication skills,HIPAA,Computer Skills,Infection Control Training,Chairside Assisting,Dental Office Experience,OSHA,Medical Imaging,Outside Sales,Eaglesoft Experience: years Vacancy: 1

Scroll down for a complete overview of what this job will require Are you the right candidate for this opportunity.At Colten Care we are proud to offer career development opportunities and a range of pay enhancements across our roles.Were looking for an enthusiastic and dedicated individual to join

A leading veterinary care provider in the UK is seeking a Veterinary Care Assistant to join their team in Wexham Court. Successful candidates will work well in a team, remain calm under pressure, and be flexible learners.

Job Description ABOUT THE ROLE As a Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve. As a Care Assistant, you could be doing anything from supporting residents with their food and drink and following ca

Job Description ABOUT THE ROLE As a Senior Care Assistant at a Barchester care home, you'll look after the different needs of our residents to enable us to deliver quality, person-centred care and support. Many of our Senior Carer Assistants progress into Care Practitioner, Regional Carer or nursin

Job Description Explore a rewarding career path as a Veterinary Surgeon at a prestigious veterinary practice near Slough.

Join Mountain Healthcare, one of the UK's leading providers of forensic healthcare and sexual assault referral services.

Job Description ABOUT THE ROLE As a Bank Activities Coordinator at a Barchester care home, you'll help to create a stimulating environment that enables us to deliver exceptional all-round care and support for our residents. Meanwhile, your infectious enthusiasm and creative approach will inspire ou

Job Description UK Intern - Medical Affairs (Medical Operations) at Kyowa Kirin International plc Marlow, Buckinghamshire (hybrid) WE PUSH THE BOUNDARIES OF MEDICINE. LEAPING FORWARD TO MAKE PEOPLE SMILE At Kyowa Kirin International (KKI), our purpose is to make people smile.

Job Description ABOUT THE ROLE As a Bank Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve. ABOUT YOU To join us as a Bank Care Assistant you'll need to have some experience of caring for older people, a

Sanctuary Personnel, an innovative and committed recruitment agency has a new permanent position available for a Social Worker within the Safeguarding Pod Team to work full time based in Maidenhead.

Consultant Radiologist - Breast.

A healthcare service provider in Slough seeks Advanced Mental Health Practitioners to enhance children's mental health care.Candidates should have relevant qualifications and experience with mental health assessments.This full-time role involves urgent care responsibilities, team collaboration, and

A leading healthcare provider in the UK is seeking an Advanced Mental Health Practitioner to join their Rapid Response Team in Slough.The role involves assessing urgent mental health needs in children and young people, providing tailored care, and collaborating with various agencies.Candidates shoul

This is a fantastic opportunity to start your career in a hands‑on Technical Apprenticeship within our Materials Laboratory team.You'll be based on site, working alongside experienced technicians who will support you as you learn how to sample, test and report on the quality of our sand, aggregate

Berkshire Healthcare NHS Foundation Trust is a specialist mental health and community health services trust. Free parking across Trust sites. Act as the link between the Trust Drug and Alcohol Specialist, community drug and alcohol teams and the acute hospital specialist.

We are seeking an experienced and compassionate Band 6 Lung Cancer Clinical Nurse Specialist (CNS) to join our multidisciplinary lung cancer team. You will work closely with the lung cancer MDT, including respiratory consultants, oncologists, radiologists, specialist nurses, allied health profession

A leading community healthcare provider is seeking a Community Sister/Charge Nurse to support a team delivering excellent care.The role involves managing a diverse caseload of patients while providing leadership and clinical guidance.Ideal candidates will have a nursing qualification and experience

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and

A leading healthcare provider in Slough is looking for Consultant Dermatologists to deliver high-quality care in dermatology clinics.This part-time position offers flexibility and autonomy, allowing you to structure your own clinics.You'll manage various dermatological conditions while participating

Join a dedicated team focused on tackling NHS waiting lists and delivering high-quality outpatient services.

Previous experience of working as a Clinical Nurse Specialist. We are seeking an experienced and compassionate Band 6 Lung Cancer Clinical Nurse Specialist (CNS) to join our multidisciplinary lung cancer team. Registered Nurse with current NMC Registration.

The East Berkshire Psychological Medicine Service is part of the Berkshire urgent care pathway, and we are keen to develop staff to ensure the service comprises highly skilled and competent professionals. You will work alongside both the working age team and the older adult team within the East Berk

Frimley Health NHS Foundation Trust is committed to being an inclusive and disability confident employer and has been awarded the Gold for the Armed Forces Employment Recognition Scheme. Access to staff wellbeing initiatives, flexible working options, and an excellent NHS benefits package.

Frimley Health NHS Foundation Trust serves a population of over 900,000 people across Berkshire, Hampshire, Surrey and South Buckinghamshire, and remains committed to improving the health and wellbeing of our communities. We continue to invest heavily in our services and facilities, including the ne