Biotechnology Jobs

Basecamp Research · London

Serves as connective tissue across Global Research, Data Science and Science teams, coordinating external sequencing vendors, research partnerships and publication timelines. Owns cross-functional process improvement and tooling oversight, ensuring training data stays synchronised with frontier AI model releases. Reports to the VP of Global Research with dotted-line alignment to the Founding TPM.

Basecamp Research · London

Runs a high-throughput sample processing pipeline, performing DNA extraction, normalisation and library preparation on soil, faecal and other environmental samples. Operates automated liquid handling platforms such as Myra9, logs everything in Benchling LIMS, and carries out QC checks while supporting R&D protocol testing in a CL2 lab.

Mytos · Stevenage

Lead the push for an MHRA MIA(IMP) licence at the first site of an automated CDMO for regenerative medicine, establishing and maintaining a scalable PQS and ensuring production complies with quality policies. The role covers audit leadership, inspection readiness, quality strategy with leadership, and preparing for future commercial batch release, working alongside advisors from Catalent and Resilience.

Orchard Therapeutics · London

Safety expert serving as global PV lead for gene therapy products across investigational and marketed phases, owning benefit-risk strategy, aggregate reports (PSURs, DSURs) and risk management plans. Also acts as medical monitor, providing clinical oversight, real-time AE/SAE review and signal detection in close collaboration with cross-functional teams and health authorities.

Autolus · London

Primary point of contact for Advanced Therapy Treatment Centres in the South UK, driving appropriate utilisation of CAR T therapies and coordinating site qualification, setup and patient treatment logistics. Works cross-functionally with Marketing, Medical Affairs and Market Access, and is 80% field based with UK travel.

Gilead Sciences · Uxbridge

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Autolus · US - East Coast

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.

CSL · Maidenhead

Oversees vendor delivery of medical evaluations for individual case safety reports, applying medical and scientific judgment on causality, expectedness and seriousness. Trains Medical Evaluators, sets assessment frameworks and drives process improvements across Global Safety and Pharmacovigilance. Requires deep pharmacovigilance knowledge and cross-functional stakeholder work.

CSL · Maidenhead · US$212,000 – US$251,000 pa

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

Thermo Fisher Scientific · United Kingdom

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.

AstraZeneca · Manchester

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You will build stakeholder partnerships, support research and evidence generation, and use digital channels and insight-led planning to demonstrate medical impact while complying with the ABPI Code.

AstraZeneca · Liverpool

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You will plan territory engagement, build stakeholder partnerships, support research and evidence generation, and use digital channels to demonstrate medical impact while complying with the ABPI Code.

IQVIA · London

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.

Fortrea · Maidenhead

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

Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.