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Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;. Clinical Trial Managers with expertise in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise. Medpace is the leading CRO for Biotech companies and is continuing to

The Clinical Scientist supports the design, execution, and analysis of clinical trials that are part of AIRNA’s RNA editing platform. Working closely with Clinical Development, Clinical Operations, and external clinical trial site staff, the clinical scientist will ensure scientific integrity and

The role of the Senior Clinical Trial Administrator (Sr CTA) is to perform daily administrative activities and support the Project Manager(s), Project Director(s) and cross-functional study team(s) through expert knowledge and effective use of the systems, tools and processes available with a focus

Keywords: Statistical, Genetics, Genomic, Data, Clinical, Trial, WGS, Omics, Pharmaceutical, Industry, Biotech, Research, Development, PRS, Polygenic, Scores, Analysis, Patient, Stratification, Selection, Bioinformatics, Project, Leader, Principal, Cross-functional, Teams, Stakeholder, Scientific, Q

We're currently partnering with a leading international pharmaceutical company to recruit a Junior CRA. Location: West London Hybrid: Twice a week in office DESCRIPTION OF THE ROLE • Site evaluation and setup for commercial distribution including training of dosing in collaboration with the Clinical Project Manager or designee, • Maintenance of contacts with sites for commercial distribution and sites which may be involved in clinical trials, • Collection of essential documents according to ICH-GCP E6 (R2) and applicable regulations, • Monitoring of data collection and pharmacovigilance/ safety reporting at the sites where a post authorisation study is conducted, • Site setup, initiation, close-out and management (including monitoring) of sites participating in clinical and post-authorisation studies on an as needs basis, • Site management including site supplies, site payment process, etc., • Study/clinical trial status tracking and progress update to team, • EC/IRB and regulatory submissions, • Participation in investigator meetings and other meetings as necessary, • Attendance of conferences as applicable, • Contribution to other tasks such as creation of newsletters as directed by the Clinical Project Manager or designee, • Assist with audits as required, • Contribute to initiatives and process improvements as required, • Contribute to Literature Reviews. KEY RESULT AREAS • Feasibility assessments/visit evaluations for clinical and post-authorisation studies, • Site setup for commercial distribution according to post-authorisation requirements, • Site setup for clinical trials (as needs basis), • Site management: investigating, following up and escalating site issues as needed., • Delivery of data accuracy through CRF review through on-site and remote monitoring according to the risk-based monitoring plan to ensure patient safety, compliance and decreased risks., • Assistance with pharmacovigilance, safety reporting management and investigations of quality complaints, • In-house/ on-site document quality management (including, but not limited to, trial master file, investigator site file). QUALIFICATIONS/EXPERIENCE • Graduate qualifications in Biological Sciences, Nursing, Pharmacy or related discipline, • Post-graduate qualifications desirable, • At least 2 years proven experience as a CRA, • Working knowledge of ICH GCP guidelines, • On-site experience, • Proven experience in managing clinical trials/projects WHAT'S ON OFFER • A competitive salary with benefits., • The chance to contribute and be part of team whose work directly benefits healthcare and strives to improve people's lives., • A real hands-on opportunity to gain a high degree of commercial exposure., • The chance to work alongside world-leading scientific experts., • Working with highly-talented and dedicated colleagues in a fast-growing company that combines a focus on cutting-edge science with commercial delivery. Interested in making a difference? Apply now or reach out to learn more about this exciting opportunity!

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide bio

We're currently partnering with a leading international pharmaceutical company to recruit a Senior Clinica Reasearch Assocaite. Location: West London Hybrid: twice a week in office Job Summary • Feasibility assessments/ visit evaluations for clinical trials., • Site setup for commercial distribution and for clinical trials, • Study management, • Site management investigating, following up and escalating site issues as needed., • Conduct remote and on-site visits in accordance with the protocols, GxP guidelines, applicable local and international regulations and company SOPs to ensure subjects rights, well-being and data reliability, ensuring audit readiness., • Relationship management with site staff, • Assistance with pharmacovigilance, safety reporting management, • In house/ onsite document quality management Responsabilties Include, but are not limited to: • Management of studies, • Site evaluation and setup for commercial distribution including site training, • Maintenance of contacts with sites for commercial distribution and sites which may be involved in clinical trials, • Collection of essential documents according to ICH-GCP, GVP and applicable regulations., • Monitoring of data collection and pharmacovigilance/ safety reporting at the sites where a study is conducted, • Site setup, training, initiation, close-out and management (including monitoring) of studies, • Site management including site payment process and reconciliation, • Study/clinical trial status tracking, QC and progress update to team, • Prepare or Review of site visit reports, • Participation in investigator meetings and other meetings as necessary, • Attendance of, and representation at, conferences as applicable, • Contribution to other tasks such as creation of newsletters as directed, • Assist with inspections/audits as required, • Contribute to the preparation of the CSR/publications, informed consents, protocols, and guidelines, sharing ideas with study members, • Prepare documents such as informed consent, monitoring plans and study operating manual for studies., • Assist in creating project specific training for more junior members and sites, • Takes initiative to identify areas for potential process improvements, bringing these to the attention of the Clinical Operations Manager, • Preparation of Literature Reviews and searches Senior Clinical Specialist, • Contribution to scientific discussions regarding therapeutic areas, treatments, study endpoints and investigational medicinal products. QUALIFICATIONS/EXPERIENCE • Graduate qualifications in Biological Sciences, Nursing, Pharmacy or related discipline, • Post-graduate qualifications desirable, • At least 4 years proven experience as a CRA, • On-site experience, • Working knowledge of ICH GCP guidelines, • Proven experience in managing clinical trials/projects WHAT'S ON OFFER • A competitive salary with benefits., • The chance to contribute and be part of team whose work directly benefits healthcare and strives to improve people's lives., • A real hands-on opportunity to gain a high degree of commercial exposure., • The chance to work alongside world-leading scientific experts., • Working with highly-talented and dedicated colleagues in a fast-growing company that combines a focus on cutting-edge science with commercial delivery. Interested in making a difference? Apply now or reach out to learn more about this exciting opportunity!

Job Title: Contract Clinical Project Manager.Location: South East, UK (Hybrid/Flexible Working Options).We are a dynamic, mid-sized Clinical Research Organisation (CRO) with a strong reputation for delivering high-quality clinical trial services across Europe and beyond.With a focus on cutting-edge

Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). Deliver high-quality CMC re

London (hybrid) or home-based anywhere in Europe.We’re working with a growing mid-sized CRO that’s looking for an experienced and hands-on Clinical Trial Manager to join their team.This is a great opportunity for someone who enjoys being closely involved in all aspects of trial delivery – from

Hobson Prior is seeking a Japanese-speaking freelance clinician to support clinical trial activities in Alzheimer's Disease.

Associate Director, AI Data Scientist.AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare.This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D

. Ready to lead projects that bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference! Proclinical is seeking a Clinical Operations Lead to support the delivery of clinical trials in oncology. In this role, you will lead or contribute to cross-functional global teams, ensuring operational excellence across all phases of clinical studies. This position focuses on driving innovation in clinical trial delivery, with the patient at the center of all activities. Please note that to be considered for this role you must have the right to work in this location or hold an EU passport. Responsibilities: • Develop and manage operational plans, including clinical study budgets, to ensure consistency and efficiency., • Oversee vendor and stakeholder relationships, ensuring performance and alignment with project goals., • Establish yourself as a leader within the team, inspiring others and sharing best practices., • Manage risk and compliance by implementing site monitoring and risk mitigation strategies, adhering to ICH-GCP and other regulations., • Oversee resource management, including forecasting and maintaining supplies for clinical studies., • Lead feasibility assessments to select appropriate countries and sites for trial participation., • Provide guidance to country operational representatives and maintain strong external stakeholder relationships., • Contribute to clinical operations communities, enabling innovative trial delivery and addressing emergent needs. Key Skills and Requirements: • Strong leadership skills with the ability to guide teams in executing clinical studies from start to finish., • Working knowledge of the drug development process and regulations, including ICH-GCP guidelines., • Experience in clinical trial management, with a focus on operational efficiency and stakeholder collaboration., • Ability to thrive in fast-paced, collaborative environments and adapt to ambiguity., • A university degree or equivalent experience, preferably in life sciences. If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at . Apply Now: If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

About the Citrin Foundation The Citrin Foundation is a research-oriented non-profit organization committed to identifying a cure for citrin deficiency—a monogenic metabolic disorder—and supporting affected individuals throughout their lives. The Foundation’s mission is to drive scientific progress and accelerate the development of effective therapies that improve patient outcomes and quality of life. We are currently seeking a Clinical and Translational Research Program Manager to join our team. This position offers an opportunity for experienced clinical and translational research professional to contribute meaningfully to the advancement of translational science within a dynamic and mission-driven organization. The ideal candidate will demonstrate both leadership capabilities and a willingness to be hands-on in the execution of research activities. You will be able to find out more about us on our website here: ___ You will be able to find out more about us on our website here: Position Summary The Clinical and Translational Research Program Manager will be responsible for the implementation and operational management of the Foundation’s clinical and translational research portfolio. This individual will support the Foundation in translating scientific discoveries into therapeutic applications, facilitating collaborations between academic researchers, clinical teams, industry partners, and the patient community. Given the Foundation’s small team structure, the successful candidate must be comfortable working with external stakeholders, researchers as well as execution of clinical and translational research-related activities. This role requires strong project management skills, a solid understanding of clinical research processes, and a commitment to advancing patient-centered solutions in the field of rare disease. Key Responsibilities Management of Clinical and Translational Research Initiatives • Coordinate and oversee research projects funded by the Foundation, ensuring alignment with organizational objectives and timely execution of project milestones., • Evaluate and support new research opportunities with high translational potential., • Monitor study progress, budgets, and deliverables in close collaboration with internal and external stakeholders. Facilitation of Cross-Sector Collaboration • Serve as the point of contact between academic investigators, clinical collaborators, industry stakeholders, and patient representatives., • Foster effective communication and alignment across all parties to support successful project implementation. Support of Translational Activities • Work with research teams funded by the Foundation to support the translation of basic scientific findings into clinically applicable therapies., • Assist in addressing logistical, operational, and regulatory challenges encountered during the translational process. Protocol Development and Regulatory Compliance • Contribute to the design and review of study protocols, informed consent documents, and related materials., • Support the preparation of ethics and regulatory submissions in accordance with relevant standards and requirements. Patient Recruitment and Engagement • Collaborate with the Foundation’s patient engagement team to support recruitment strategies and ensure study designs are patient-centered and accessible. Coordination of Natural History Studies • Lead the planning and operational management of natural history studies, including oversight of data collection and coordination with research partners., • Ensure that data generated informs future therapeutic development and clinical trial design. Qualifications Education • Advanced degree (PhD, MD, MSc, or equivalent) in life sciences, medicine, or a related discipline. Experience • A minimum of 3 to 5 years of experience in clinical research or translational science, ideally within academic, hospital-based, or industry settings., • Experience in early-phase studies, rare diseases, or investigator-led clinical trials is strongly preferred., • Demonstrated ability to lead projects while remaining actively engaged in day-to-day operations. Skills and Competencies • Thorough knowledge of clinical study or trial design, research operations, and regulatory requirements., • Strong organizational, time management, and problem-solving skills., • Excellent written and verbal communication skills, with the ability to interface effectively with both scientific and non-scientific stakeholders., • Capacity to work both independently and collaboratively in a multidisciplinary environment., • Deep commitment to the mission of improving outcomes for individuals with rare diseases. Why Join Citrin Foundation? • Impactful Work: Play a direct role in research that has the potential to transform the lives of individuals with citrin deficiency and beyond., • Global Collaboration: Work with experts from around the world in a collaborative environment that fosters innovation and meaningful change., • Growth Opportunities: Expand your career and develop professionally while contributing to the growth of a mission-driven organization., • Patient-Centered Focus: Contribute to research that is centered around improving the lives of patients and their families, making a real-world impact.

Proclinical is seeking an Associate Director Biostatistics to join a dynamic team in London, UK. This hybrid role offers the opportunity to work on innovative clinical trials in the rare disease space, contributing to the development of groundbreaking therapies. You will collaborate with cross-functional teams, oversee statistical activities, and play a key role in shaping trial designs and data analysis. Responsibilities: • Represent biostatistics in cross-functional team meetings to support clinical development plans., • Collaborate with Clinical Development, Regulatory, and Clinical Operations teams to design clinical trials., • Author statistical sections of clinical trial protocols and analysis plans., • Oversee the design of electronic case report forms (eCRFs) in collaboration with Data Management., • Provide statistical guidance during the conduct of ongoing trials., • Work with Statistical Programmers to summarize and analyze trial data., • Contribute to clinical study reports and regulatory documents such as DSURs and briefing documents., • Represent the organization in meetings with regulators, key opinion leaders, and other stakeholders., • Support the preparation of scientific articles summarizing trial data., • Consult with preclinical and research teams on statistical questions., • Manage CRO statistical and programming support. Key Skills and Requirements: • Advanced degree (PhD or MS) in Biostatistics, Statistics, or a related field., • Proficiency in SAS programming and familiarity with R programming., • Strong written and oral communication skills., • Experience with CDISC standards, including SDTM, ADaM, and CDASH., • Knowledge of ICH GCP guidelines and industry practices., • Experience designing adaptive trials and working through Phase 3 and NDA submissions., • Ability to represent sponsors in regulatory meetings., • Interest in biology and biological processes, including RNAi therapeutics. If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at . Apply Now: If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

We're currently partnering with a leading international pharmaceutical company to recruit a Clinical Program Lead. ABOUT THE ROLE The Clinical Program Lead is responsible for activities including design, monitoring, data interpretation and reporting related to the conduct of interventional and/ or non-interventional clinical studies, in accordance with applicable regulations, ICH/GCP regulations and Standard Operating Procedures (SOPs) within one specific assigned program. Clinical Program delivery • Support the Director, Global Clinical Affairs in the implementation of the vision for Clinical Affairs that drive the quality, cost, speed and efficiency of clinical studies delivery., • Implement the program strategy and contribute to the overall strategy of the Clinical Affairs department along with other Clinical Program Leads., • Maintain an overview the program status and issues and proactively communicates to the Director, Global Clinical Affairs progress, risks, issues or changes that may impact quality, timelines and/or budget; provides clinical program level updates as requested., • Engage cross functionally to ensure transparency, transfer of knowledge and alignment within the program., • Areas of focus for execution and oversight include, but not limited to:, • Building expertise and keeping up to date in the scientific aspects of the program e.g. scientific literature, • Protocol development, implementation of Quality by Design principles o Study Monitoring, oversight of data quality and integrity, and safety and rights of participants o Data management, data cleaning activities according to timelines Reporting, analysis review and Clinical Study Report development, • Clinical sites: selection, contract development, budget negotiation and monitoring, recruitment, regulatory and ethics submissions requirements, maintain relationships with principal investigators and/ or expert physicians, investigators meetings (including site initiation visits/ accreditation), support Clinical Study Leads/ Clinical Project Associates in management and oversight., • Service providers: selection, contract development and budget negotiation and monitoring, support Clinical Study Leads/ Clinical Project Associates in management and oversight of activities and performance., • Records management • Implement and ensure inspection readiness within the program; and supports GCP audits and inspections. Clinical Program enabling activities • Implement activities and initiatives that support the program and study(ies) delivery and overall portfolio efficiency. This includes, but not limited to, processes enhancement, modernisation of clinical trials (i.e. digital integration) and transfer of knowledge. People Management:, • Provide leadership, support, feedback, coaching and mentoring to the core Study Management Team., • Direct reports within the Clinical Operations team., • Support the Director Clinical Affairs with professional development for Clinical Operations Team., • Resource management within the Clinical Program i.e. delegate, as appropriate, to assign responsibilities to project team members., • Assist in the training of relevant staff as needed. Other, • Support development of external communications related to clinical program and studies., • Attend conferences and external events., • Attend meetings with National Competent Authorities, where required., • Organise and lead regular internal clinical team meetings., • Organise and lead internal trainings. QUALIFICATIONS/EXPERIENCE • Graduate qualifications in Biological Sciences, Nursing, Pharmacy or Medicine (post-graduate qualifications desirable), • Working knowledge of international clinical research regulations and requirements ICH/GCP guidelines, • Proven experience in management of clinical trials in EU, • Established and managed a clinical trial program in EU, • Working knowledge of data management, • Excellent communication skills, both written and verbal, • Project management skills, • Independence and the ability to lead a team effectively, • Observational and analytical skills, • Good time management and the ability to work to tight deadlines, • Ability to problem solve and make decisions quickly WHAT'S ON OFFER • A competitive salary with benefits., • The chance to contribute and be part of team whose work directly benefits healthcare and strives to improve people's lives., • A real hands-on opportunity to gain a high degree of commercial exposure., • The chance to work alongside world-leading scientific experts., • Working with highly-talented and dedicated colleagues in a fast-growing company that combines Interested in making a differnece? Apply now or reach out to learn more about this exciting opportunity!

Clinical Negligence Solicitor / Lawyer - Remote The Role This is a superb opportunity to join an award-winning Top 100 law firm that offers specialist quality legal advice to both businesses and individuals nationwide. Due to the development and expansion of the firm’s Clinical Negligence department, it is now seeking to appoint a Solicitor/Legal Executive to take on some excellent cases and work on them from inception to trial. The ideal candidate will have experience handling a caseload of Clinical Negligence claims, investigating and litigating multi-track cases. You must ensure cases are progressed in a timely, efficient and proactive manner and meet all KPI targets set by the firm. This firm currently has a team of experts and are keen to speak to likeminded people, who are passionate about Clinical Negligence and client care. The Candidate • Clinical Negligence Solicitor / Legal Executive handling own caseload (2+ years experience), • Experience of drafting legal documentation, • Prioritise and manage a varied caseload, • Ability to work well as part of a team and on your own initiative, • Excellent organisation and time-management skills, • Excellent client care skills, • Professional and effective communication with team members and contacts The Benefits & How to Apply • Salary, dependent upon experience/PQE - plus an annual bonus, • 35 days annual including bank holidays and Christmas Closure, • Hybrid and flexible working, • Ongoing training and development opportunities, • Social events and charity fundraising days, • Enhanced maternity/paternity pay Apply in the strictest of confidence online and or via telephone – there is no need for a CV for an initial conversation. Contact Roya Ratcliffe Retained Consultant – INDRR Direct Dial: 0161 826 3140 Mobile: 07376 640524

Job Title: Laboratory Manager Location: London, UK Job Type: Permanent Are you ready to lead in a fast-paced, high-impact lab environment? This is an exciting opportunity to take charge of clinical diagnostics and trial operations driving accuracy, efficiency, and excellence while ensuring full compliance with industry standards. Responsibilities: • Oversee daily clinical and trial sample testing, ensuring compliance with ISO 17025, ISO 15189, GCP, and MHRA guidelines., • Work with QA teams to maintain effective and compliant testing procedures., • Monitor IQC/EQA performance and take corrective action when needed., • Supervise and support lab staff, including training and performance reviews., • Maintain sample integrity, review analytical data, and approve new test methods., • Draft and update SOPs and liaise with clients to ensure quality service. Experience and Qualifications Required: • Strong leadership experience in a lab setting., • Degree in Biomedical Science, Biochemistry, Chemistry, Immunology, or related field., • Previous experience as a Scientist or Lab Analyst., • Excellent communication, organizational, and team development skills. How to apply: Apply to to learn more about the role or connect with me on LinkedIn to hear about regular job updates available with X4 Life Sciences.

About the Role We are seeking a dedicated and experienced Principal Investigator (PI) to join our expanding UK clinical research team. This is a hybrid position, combining remote medical oversight with regular on-site responsibilities across our network of clinical research sites. The PI will act as the medically accountable lead for assigned studies, ensuring trials are conducted to the highest scientific, ethical, and regulatory standards while safeguarding participant safety. Key Responsibilities Medical & Regulatory Oversight • Serve as the Principal Investigator for clinical trials, providing overall medical leadership and accountability., • Ensure strict compliance with study protocols, ICH-GCP, UK Clinical Trial Regulations, MHRA guidance, and local SOPs., • Conduct or oversee medical eligibility assessments, patient histories, and trial-specific examinations (on-site as required)., • Review and sign off informed consent forms, patient safety data, and study documentation. Participant Safety & Clinical Care • Monitor participant safety throughout the duration of studies, making clinical decisions regarding treatment continuation or withdrawal., • Report SAEs, SUSARs, and AEs in accordance with regulatory timelines., • Act as the key medical contact for participant concerns, clinical queries, and emergency oversight. Leadership & Collaboration • Provide guidance and mentorship to research staff, including sub-investigators, nurses, and coordinators., • Build strong relationships with sponsors, CROs, and regulators., • Participate in site selection, feasibility assessments, and audits. Hybrid Work Model • Remote responsibilities include: protocol review, safety oversight, medical queries, and teleconferences with sponsors/CROs., • On-site responsibilities (at least 1–2 days per week, depending on study requirements) include: patient assessments, staff training, monitoring visits, and audits. Qualifications & Experience • Medical degree (MBBS/MBChB or equivalent) with full GMC registration and licence to practise in the UK., • Previous experience as a Principal Investigator and Sub-Investigator required, but experienced clinicians with a strong interest in research will also be considered., • Solid understanding of ICH-GCP, UK Clinical Trial Regulations, and MHRA requirements., • Excellent leadership, communication, and organizational skills., • Ability to balance remote work efficiency with on-site clinical commitments. What We Offer • Flexible hybrid working model (remote + site-based)., • Opportunity to lead high-impact clinical trials across a range of therapeutic areas., • Professional development and training in clinical research leadership., • Collaborative working culture with supportive multidisciplinary teams., • Competitive salary and benefits package. Key Competencies • Clinical expertise and sound decision-making., • Strong grasp of regulatory and ethical frameworks., • Effective communication and team leadership., • Adaptability to both virtual and on-site working environments., • Commitment to patient-centred care and research excellence.

Role: Principal Scientist, CMC Location: London, UK (3 days/week on-site) The Company A pioneering cell therapy biotech is on a mission to transform the treatment of solid tumours through a unique allogeneic neutrophil-based therapy platform. Unlike patient-specific T-cell therapies, this approach is donor-derived, scalable, and consistent, enabling manufacturing at scale and efficient delivery to patients. The therapy harnesses the natural tumour-infiltrating and tumour-killing abilities of neutrophils, which can also be engineered to enhance anti-cancer activity. This makes the platform a differentiated strategy designed to overcome tumour resistance and improve outcomes. The company is entering an exciting growth phase, with its first-in-human clinical trial scheduled in Ireland within the next 12 months. GMP manufacturing is supported by a specialist CDMO partner, while the UK headquarters drive innovation, translational research, and CMC strategy. With strong leadership, a visionary platform, and a clear clinical path ahead, this is a rare chance to contribute to next-generation oncology therapies at the point where science is translating into patient impact. The Team The role reports directly to the CSO and will initially include line management of one scientist, with scope to expand later in the year as grant funding is activated. The Opportunity This is a chance to lead CMC strategy at a high-growth biotech on the cusp of clinical development. You will directly shape GMP compliance, tech transfer, and regulatory governance while building and leading a small team. The role offers exposure to a cutting-edge oncology platform with significant potential impact. Key Responsibilities • Lead CMC activities and strategy for the neutrophil therapy platform, • Ensure GMP compliance of process and documentation, • Oversee tech transfer to a specialist CDMO partner in Ireland, • Write and manage EU/IE regulatory submissions, • Work cross-functionally with translational and clinical teams, • Report directly to the CSO, • Line manage one direct report, with potential to grow the team later this year Requirements • Strong CMC experience in cell therapy, ideally oncology, • Proven track record leading GMP compliance and governance in a biotech or CDMO environment, • Experience with CDMO oversight and successful tech transfer projects, • Knowledge of EU/IE regulatory requirements for CMC submissions, • Previous experience managing or mentoring junior scientists, • Based within commuting distance of London (3 days per week on-site), • Willingness to travel occasionally to Ireland

Clinical Trial Manager – Virology | London (3-5 Days Onsite). As Clinical Trial Manager, you will play a pivotal role in managing regional components of global studies, ensuring timely delivery and quality execution in partnership with CROs and cross-functional teams. Lead and influence multiple v

If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us. Successful execution of assigned trials and ensuring completion of trial deliverables. Precision for Medicine is looking for an e

Clinical Trial Liaison – Oncology (Europe, Field-Based).An innovative global biotech company is seeking a Clinical Trial Liaison to drive site and patient engagement for oncology trials across Europe, with a focus on breast cancer and other high-priority indications.Build relationships with KOLs,

Bionical Emas is a global Early Access Programs (EAP) and Clinical Trial Supply (CTS) group bringing life-changing medicines to patients around the world.Their range of services and capabilities benefit many of the worlds leading pharma and biotech companies.At Bionical Emas you will have the chance

ARTO is currently partnered with a globally renowned mid sized Pharmaceutical company who are committed to the development of drugs within the Rare Disease space. Within their Global Clinical Operations team, they are looking for an Associate Director who will be able to lead Clinical programs and projects as well as manage a cross functional group to execute complex trials. Key Responsibilities: • Contribute to clinical strategies for programs, providing leadership on the design and excecution of CDPs, • Provide guidance on all relevant program and study deliverables, • Provide program-level oversight, leadership, and direction ensuring Operations team members achieve deliverables within timelines, budgets and in accordance with GCP and company standards., • Give strategic guidance and reports on program progress, risks, issues and metrix as needed to executive leadership., • Drive cross functional initiatives across the portfolio of programs . Qualifications: • BA/BSc/PhD with a focus on life sciences, • 10 Years experience within biotech and pharmaceutical companies leading clinical trial or drug development initiatives., • Team management experience If this role could be something of interest to you, please feel free to apply through the job advertisement or reach out to me at -

Medical Science Liaison – London Area Pharma-Partners is exclusively recruiting for this vacancy. The territory for this role includes London, North London Counties and East Anglia. We are looking for a current UK based Medical Scientific Liaison looking to progress and take on more responsibility in a smaller company. Working alongside a team of Senior MSLs and MSLs, this role will support a small portfolio of treatments that relate to a wide variety of therapy areas. The Medical Science Liaison will focus on establishing and maintaining relationships with KOLs across the territory, drive and lead medical education activities such as advisory boards and steering committees, be involved in IITs and work closely with the field Commercial team in a collaborative manner to enhance insight gathering. For this vacancy our client is seeking candidates with circa 2 years of UK MSL experience. They offer a clear pathway for MSLs to achieve Senior MSL level with the support and coaching from the hiring manager and peers across the Medical Affairs team. Key Responsibilities: • Act as a scientific expert, • Engage with KOLs in scientific exchange, and develop and maintain meaningful relationships across the territory, • Share relevant insights within medical and cross-functional teams, • Support and deliver medical training of commercial field teams, • Involvement in UK clinical research activities, • Ensure adherence to company SOPs and the ABPI Code, • Input into cross functional plans and provide scientific expertise and advice as needed, • Represent the business and medical team at local, regional and global congress and symposia The Candidate: • Relevant Science based degree with advanced Degree level seen as desirable, • MSL experience in the UK is essential (preferably 2 years+), • Demonstrable experience in building and maintaining KOL relationships, • Knowledge of clinical trial processes and regulatory requirements, • Any therapy area background can be considered, • Experience in and knowledge of the UK healthcare systems, • Effectively assimilate scientific and clinical data to the relevant audience To Apply: To apply for this position please use the “Apply” option or feel free to send your CV directly to the Pharma-Partners team via email

The Principal, AI Data Scientist will be responsible for supporting the implementation of innovative, complex and transformative AI/ML/GenAI solutions across the areas of Clinical Trial Execution and Digital Healthcare across Jazz Research and Development.Support the development and implementation o

Ensure compliance with relevant regulations/guidelines such as Good Clinical Practice (GCP) throughout all stages of clinical trial material/services procurement. Collaborate closely with cross-functional teams including Operations personnel (clinical operations teams), quality assurance/quality con

Principal Biostatistician (Medical Affairs) Europe and NA Based. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Must have lead experience within Medical Affairs in a clinical trial setting.

The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Compile and maintain project-specific status reports within the clinical trial management system. Candidates should expect to have an intensive training period and show th

PhDs and/or Post-Doctoral Research experience. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and.

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling. Minimum of 2 years of Clinical Trial Management experience, CRO exp

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in thei

At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. Clinical Trial Pharmacovigilance experience.

Clinical Trial Manager I - 3 days a week in Uxbridge (Gene and Cell therapy exp needed).

Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Communicate and collaborate on global study activities; working closely with the Projec

The Research Nurse/Clinical Trials Practitioner is an autonomous specialist working within the multi-disciplinary team. The post holder will be responsible for the coordination and management of a clinical research portfolio comprising in-house, national, and international phase II and III clinical

Strong understanding of the clinical trial process and clinical trial protocols. In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient travel and reimbursements, and Scout Academy, our secure, online, on-demand

Co-ordinate and maintain the Clinical Trials service in accordance with current UK Clinical Trial Regulations, the Medicines for Human Use (Clinical Trials) regulation 2004 (EU Clinical Trial Directive) and all updates, together with ICH GCP guidelines and departmental procedures and ensure provisio

At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. Company-sponsored employee appreciation events.

WTE) - Mood Disorders Research Clinic.WTE Staff Psychiatrist within the Mood Disorders Research Clinic, supporting clinical trial activity and research in mood disorders at North London NHS Foundation Trust.London, and is available from July 2025.The post holder will play a key role in the treatment

Sr Clinical Trial Manager (Global Clinical Ops) UK based Only. Core Focus • Overseeing the development, coordination, and implementation of Phase 1 clinical research studies • Collaborating with principal investigators, research subjects, client teams, investigators, and clinic operations teams

Access Programs Clinical Trial ServicesPatient Site SolutionsClinical Trial SupplyMarket Access and Commercialization. WEP Clinical has over 15 years of experience distributing products to over 120 countries worldwide to treat unmet patient needs. Work with the supply chain team to coordinate and di

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling. Minimum of 2 years of Clinical Trial Management experience, CRO exp

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred;. Clinical Trial Manager - UK (

At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. Company-sponsored employee appreciation events.

We actively collaborate with other research centres, engage with local communities, and organise research awareness events to promote participation in studies and improve access to research opportunities. The group supports researchers at every stage—from grant applications and service development

An exciting opportunity has arisen for a Clinical Trial Research Nurse in the Urology team as part of the Cancer Research Delivery Group (CRDG) at St. The post holder will take responsibility for the coordination and management of all aspects of a clinical research portfolio comprising in-house, nat