Biotechnology Jobs

• Durham, United States
• US$203,775 – US$339,625 pa
• Director

Leads the integrated real-world evidence and health outcomes strategy for mRNA influenza vaccines, designing and interpreting US post-marketing vaccine effectiveness studies across late-stage development, launch and post-marketing phases. Partners with clinical development, epidemiology, medical affairs, regulatory, biostatistics and market access teams, and builds collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR · Administrative Claims +1

• Stevenage
• Hybrid
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, covering biosample collection, processing and storage, and implementation of clinical trial assays at reference and central labs and CROs. Works in a matrix with biomarker, clinical operations, data management, regulatory and procurement colleagues, managing vendors, contracts and data transfer agreements while keeping studies audit-ready.

• Home Worker
• Remote
• £49,140 – £91,260 pa

Author and manage high-quality regulatory documents for medicines, working with cross-functional clinical and submission teams. Advise on regulatory writing standards, lead writing plans and timelines, and apply AI tools to improve quality and efficiency. Requires strong biostatistics understanding and global regulatory knowledge.

Artificial Intelligence

• Home Worker
• Remote
• £47,540 – £88,289 pa
• Mid-level

Manages regulatory activities for clinical trial applications across an assigned portfolio, leading high-quality submissions and coordinating responses to Health Authority queries. Works closely with study teams, country leads and cross-functional partners to identify regulatory risks early and secure timely approvals, while contributing to simplification and automation initiatives across Regulatory Affairs.

• London
• Lead

Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.

• Swindon
• On-site
• Shift work

Operate aseptic filling lines and manufacture pharmaceuticals to SOPs and Batch Manufacturing Records, performing filling, packaging, in-process checks, line changeovers and cleaning. Work in cleanrooms on Double Days, 24/7 or Night shifts, using HMI-controlled CIP/SIP systems, autoclaves and SAP, and support validation and new product introduction.

SAP · HMI · CIP +2

• London
• Lead

Serves as subject matter expert in COA endpoint strategy, instrument development and regulatory strategy, advising pharma and biotech sponsors and representing the company as an external scientific thought leader. Leads qualitative research supporting content validity, oversees internal project teams, mentors consultants and supports business development through proposals and client presentations.

• London
• On-site
• Director

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.

Generative AI

• Oxford
• On-site
• Entry level
• Temporary

Operate manufacturing equipment for mRNA vaccine production under cGMP and SOPs, maintaining documentation, gowning and housekeeping standards. Partner with Quality Assurance on batch disposition, lead root cause analysis and CAPA for deviations, and troubleshoot equipment and digital system issues. Work 100% onsite with digital and Generative AI-enabled manufacturing technologies.

Generative AI

• London
• On-site
• Entry level
• Permanent

Contributes to the design and execution of cellular and biochemical assays, including arrayed CRISPR perturbation screens in established cell models, and maintains primary and immortalised mammalian cell lines with sample tracking and QC. Runs phenotypic readouts such as flow cytometry, RT-qPCR and ELISA, performs data analysis and quality assurance, and reports outcomes to cross-functional project teams. Based in London wet labs within a matrixed TechBio environment.

CRISPR · Flow Cytometry · RT-qPCR +3

• London
• Hybrid
• Senior

Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.

LIMS

• High Wycombe
• Entry level
• Internship

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with SOPs and local regulatory requirements. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Microsoft Word · Microsoft PowerPoint · Microsoft Excel

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• Slough
• On-site
• Mid-level
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances in a client's Analytical Service Department, running ELISA, cell-based and Biacore assays and capturing data in laboratory software and electronic notebooks. Generates and reviews GMP-compliant documentation, SOPs and protocols, supports method development and validation, and handles out-of-specification investigations while liaising with internal and external clients.

Biacore · Vi-Cell · Microsoft Office