Biotechnology Jobs

• 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.

• Lisburn
• On-site
• Entry level
• Internship

A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.

SAS · R · MATLAB +1

• 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.

• 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

• Stevenage
• Hybrid
• Director

Leads acquisition, integration and analysis of large-scale cancer multi-omic and clinical datasets to drive translational decisions and support the oncology pipeline. Partners with biologists, clinicians, AI/ML engineers and statisticians, building reproducible data pipelines and informatics infrastructure, with mentoring responsibilities in a hybrid team.

Cloud Platforms

• 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
• 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
• €63,600 – €118,000 pa
• Lead · manages people

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.

Artificial Intelligence

• Dublin, Ireland
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

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 insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence

• Burgess Hill
• Hybrid
• £49 – £86 ph
• Lead
• Contract

Leads authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex clinical data under IVDR and GCP.

AI-enabled tools

• London
• Hybrid
• Senior

Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.

SaaS · APIs · Cloud Data Platforms

• Cambridge
• Hybrid · 3 days in office
• Lead · manages people
• Permanent

Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.

• Southampton
• On-site
• Senior · manages people
• Permanent

Field-based clinical development role leading launch and adoption of pulsed field ablation technologies (VARIPULSE, Dual Energy STSF) across southern UK EP centres. Manages four New Technology Specialists, drives site readiness, first-case support and routine utilisation, and partners with the northern counterpart to set national clinical standards.

CARTO 3 · Biosense Webster · VARIPULSE +1