Latest Therapeutics Jobs

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, approval and launch. Sets disease-area strategy, chairs governance forums and advisory boards, and line-manages clinical development leads within a global matrix. Distinct for its portfolio-level enterprise scope and hybrid US/UK/Swiss base.

GSK Upper Providence

Hybrid

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, regulatory approval and initial launch. Chairs governance forums, co-leads matrix asset teams and line-manages clinical development leads, medical directors and clinical scientists. Distinct for its portfolio-level scope across early- and late-phase programs and its cross-functional connector role spanning research, translational medicine and commercial strategy.

GSK Baar Onyx

Hybrid

Clinical Research Pharmacy Services Lead

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Ipsen London

Hybrid

Regulatory Submission Project Manager

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.

Ipsen London

Hybrid

Senior Medical Director, Global Clinical Program Lead - Immunoglobulins

The Senior Medical Director, Global Clinical Program Lead is responsible for the strategic leadership of clinical development programs, including team leadership, clinical oversight, and document authorship. The role involves cross-functional collaboration, regulatory interactions, and ensuring high scientific standards.

CSL Opfikon, Switzerland

Head of Patient-Facing Quality Assurance

Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including clinical safety interfaces, inspection readiness and CAPA frameworks. Hybrid role with global scope and international travel.

CSL Maidenhead

Hybrid

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

Moderna Oxford

On-site Temporary Clearance Required

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.

Moderna Oxford

On-site

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Leads complex global and multi-regional clinical trials from start-up through close-out, with accountability for quality, timelines, budgets, regulatory compliance and sponsor objectives. Acts as primary strategic partner to sponsors and directs cross-functional teams across regions, with a focus on renal, obesity and MASH studies.

IQVIA London

Director, Data Strategy & Partnerships

Owns the data sourcing and partnerships framework, scanning the scientific landscape for new data modalities and cohorts, negotiating access and commercial terms with biobanks, health networks and TechBios, and building business cases for data investments. Works with engineering leadership to operationalise new data sources and partners with legal, commercial and scientific leadership. Requires deep population/statistical genetics expertise and experience leading multi-institutional consortia.

Genomics London

Hybrid Permanent

Clinical Data Manager - Early Phase

Leads data management activities across early phase trials, including healthy volunteer and patient populations, multi-site studies and reduced timelines. Accountable for all DM deliverables, resource allocation, client relationships and scope changes, while mentoring the internal study team and adopting new DM technologies.

Fortrea Leeds

Hybrid Permanent

Clinical Research Associate II or Senior Clinical Research Associate

Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.

Parexel Harrow

Remote

Senior CTM, Hematology/Oncology

Accountable for delivering clean clinical data on time and within contract for low-to-moderate complexity haematology/oncology trials, managing operational and quality aspects in line with ICH GCP. Develops monitoring plans, CRF documents and Trial Master File content, tracks timelines and metrics, and may handle start-up, ethics submissions and project financials. Works within a team of CTMs, with travel to sites and a focus on radiopharmaceuticals, cell & gene therapy and CAR-T studies.

Thermo Fisher Scientific United Kingdom

Remote

Senior CRA

Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.

Fortrea Maidenhead

Lead Central Monitor

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.

Novartis London €63,600 – €118,000 pa

Hybrid