Biotechnology Jobs

• Reading
• Remote
• Lead

Lead end-to-end clinical data management for complex global trials, from study setup through database lock, acting as the primary client contact for data deliverables. Oversee SAE, PK and external data reconciliation, manage timelines and budgets, mentor junior staff, and drive process improvements using Medidata Rave or Oracle InForm.

Medidata Rave · Oracle InForm · EDC +1

• Reading
• Remote
• Lead
• Contract

Oversees end-to-end clinical data management for complex global trials, from study setup through database lock, acting as the primary client contact for data deliverables. Leads cross-functional teams, manages SAE/PK and external data reconciliation, timelines and budgets, and mentors junior staff. Fully remote with equipment provided, working across FSP delivery models.

Medidata Rave · Oracle InForm · MS Teams

• Leeds
• Hybrid
• Senior
• Permanent

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.

• Maidenhead
• Hybrid
• Senior

Leads clinical data management for one or more oncology studies within a sponsor-dedicated (FSP) model, acting as the primary client contact from study set-up through close-out. Combines strategic oversight of vendors, budgets and CDM deliverables with hands-on work such as eCRF design and data cleaning, collaborating with data coordinators and statistical programmers.

eCRF

• US - East Coast
• Hybrid
• Director

Oversees an outsourced global data management vendor across CAR T and autoimmune clinical trials, from protocol development through regulatory submission. Manages eCRF standards, data review and QC plans, database release and lock, and inspection readiness, acting as the main liaison between study teams, vendors and functional partners. Based hybrid in the UK or remote on the US East Coast.

eTMF · eCRF · SAS +2

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• London
• Hybrid
• Director · manages people

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Microsoft Office

• Waltham, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker, clinical development, regulatory and finance activities across internal groups and external partners. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Stevenage
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to progress diagnostic and biomarker development activities, coordinating with clinical, regulatory, quality, finance and external lab partners. Builds integrated timelines, tracks budgets, milestones and contracts, mitigates risks, and supports regulatory submissions and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• London
• Hybrid
• £56,511 – £104,949 pa
• Mid-level

Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.

• United Kingdom
• Remote
• Senior · manages people

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.

Outlook · Excel · Word

• Maidenhead
• Senior

Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.

Drug Safety Database

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.

• Ireland

Regional Laboratory Manager – DublinRandox are a world leader in diagnostics for clinical healthcare, toxicology, and food security. Our expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Our global success is a…