Biotechnology Jobs

• Manchester
• Mid-level

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.

Trial Master File · Investigator's Site File

• Cambridge
• Senior

Leads stem cell-focused drug discovery projects, designing and optimising human iPSC-derived models, 2D/3D assays and disease models, and applying New Approach Methodologies to client programmes. Partners directly with pharmaceutical and biotech clients, presenting data and shaping project strategy, while mentoring colleagues and contributing to proposals and capability development.

Organoids · Spheroid systems · Co-culture models +4

• London
• Hybrid
• Director

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, using Bayesian methods and simulation in R or Python, while mentoring statisticians.

R · Python

• USA - Pennsylvania - Upper Providence
• Hybrid
• Director

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, applying Bayesian methods, simulations and advanced modelling in R or Python, while mentoring statisticians.

R · Python

• 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

• Oxford
• On-site
• £39,424 – £46,476 pa
• Mid-level
• Contract

Carry out research in spatial immunometabolism focused on the germinal centre reaction within the Clarke group at the Kennedy Institute of Rheumatology. The role involves developing new scientific techniques and experimental protocols, testing hypotheses, analysing data, contributing ideas for new projects, and providing guidance to postdocs, technicians and PhD students.

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• Leeds
• Hybrid
• Entry level
• Internship

A student placement supporting the Clinical Operations team in day-to-day coordination of clinical studies, including maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies. Based in Leeds with flexibility to work remotely, though onsite working is preferred and may be required.

TMF · eTMF · CTMS +4

• Leeds
• Entry level
• Internship

A 12-month student placement in the clinical research department, supporting international trials of medical technology products. Duties include administering and coordinating the logistical aspects of clinical studies, tracking essential documents, and collecting and recording study data, with meetings alongside cross-functional partners.

Microsoft Excel · Microsoft Word · Microsoft PowerPoint

• 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.

• 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.

• London
• On-site
• £37,735 pa
• Mid-level
• Permanent

Supports the In Vivo Imaging team by running PET and SPECT imaging and biodistribution studies for internal scientists and external collaborators. Manages the nuclear imaging suite day to day, including calibrating and servicing PET-MRI, SPECT-CT, gamma counter and SARRP irradiator, radioisotope logging, waste management, SOPs and training colleagues.

PET-MRI · SPECT-CT · Micro-CT +7

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• Cambridge
• Hybrid · 3 days in office
• Director

Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.