Biotechnology Jobs

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• Reading
• Senior

Designs and builds clinical study databases, interpreting protocols and creating eCRF designs, edit specifications and EDC system configurations using CDMS tools aligned to SDTM and CDASH standards. Runs design and edit specification review meetings with data leads, programmers, validation teams, statisticians and clients, while managing multiple concurrent study builds and project financials for programming shared services.

InForm · CDMS

• Lisburn
• Senior · manages people

Senior Statistical Programmer supporting clinical trials within Parexel's FSP team, producing and QCing SDTM and ADaM datasets, tables, figures and listings using SAS. The role can act as Statistical Programming Lead, coordinating global teams, timelines and budgets while liaising with sponsors and Biostatistics and Data Management leads. It also involves mentoring staff and ensuring compliance with ICH-GCP and CDISC standards.

SAS

• Waltham, United States
• On-site
• US$150,975 – US$251,625 pa
• Mid-level

Key member of the Clinical Development team contributing to the design, execution, analysis and reporting of clinical studies across all phases. Works cross-functionally with Medical Monitoring, Clinical Operations, Biostatistics, Data Management and Regulatory Affairs, reviewing safety, efficacy, biomarker and PK/PD data and supporting CSRs and regulatory submissions. Based on-site in Waltham, MA or London, UK.

• London
• On-site

Contributes to the design, execution, analysis and reporting of hepatology clinical studies across all development phases, working with clinical operations, biostatistics, data management and regulatory affairs. Reviews safety, efficacy, biomarker and PK/PD data, supports protocol and CSR development, and engages with investigators and sites. Based on-site in London or Waltham, MA.

• London
• Hybrid
• Senior
• Permanent

Leads global pharmacovigilance operations, overseeing case intake, ICSR processing and regulatory reporting across clinical and post-marketing portfolios. Acts as business administrator for the Veeva Safety database and primary interface with PV vendors, while driving SOPs, inspection readiness and safety data exchange agreements.

Veeva Safety

• 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

• Oxford
• On-site
• Entry level

Postdoctoral researchers join an interdisciplinary team fabricating three-dimensional living, synthetic and hybrid tissues for disease modelling, therapeutic testing and organ repair. Openings span cell biology, electrophysiology, bioinformatics, hydrogel science and tissue engineering, combining stem cell biology, bioprinting and device engineering within a group of about 15 members.

Multielectrode Arrays · Calcium Imaging · Optogenetics +4

• London
• On-site
• Entry level
• Internship

A 12-month industrial placement in Pfizer's Peptide Drug Product Development group, working alongside formulation scientists and analytical chemists. The role involves preparing and evaluating peptide formulations, running solubility and stability studies, and gaining hands-on experience with HPLC/UPLC and biophysical characterisation methods.

HPLC · UPLC

• United Kingdom
• Remote
• Mid-level

Coordinates and oversees clinical trial activities for assigned studies, including regulatory document review, (e)TMF management, and site file compilation. Provides finance support such as raising POs, vendor creation, budget tracking and invoicing using CERPS, Ariba, Fiori and Veeva Payments. Trains new staff and works within a matrixed FSP team.

Veeva Payments · CERPS · Ariba +5

• 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

• Leeds
• On-site
• Entry level
• Internship

A 12-month university placement within a global clinical data management team, supporting the full clinical trial lifecycle from project documentation and system set-up to data entry, validation, reconciliation and database lock. Interns work alongside experienced Clinical Data Managers on live trials, gaining hands-on exposure to clinical research technology and processes.

• 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

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC

• Opfikon, Switzerland
• Senior

Leads safety review and end-to-end signal detection across a product's lifecycle, using quantitative and qualitative methods alongside Global Safety Leads. Contributes to aggregate safety reports, risk management plans and regulatory responses, and mentors junior PVS staff. Works cross-functionally with Development, Medical Affairs and Regulatory teams on vaccine and national-significance products.

Microsoft Excel