Latest Biotech Research Scientist Jobs

Production Sequencing Lead

This role leads the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, managing high-throughput DNA processing from extraction through to sequencing dispatch. The individual will translate R&D protocols into scalable production workflows, drive continuous operational improvements using Lean/Six Sigma, and lead a team within a fast-paced, interdisciplinary environment. They will also evaluate and integrate emerging sequencing technologies and automation to scale throughput and reliability.

Basecamp Research London, United Kingdom

On-site Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Director, Search & Evaluation Early TA Lead (CVR)

Leads strategic sourcing and evaluation of early-stage (preclinical to Phase 1) external innovation opportunities in the Cardiovascular/Renal therapeutic area. Drives due diligence, shapes partnering strategies, and collaborates with Business Development to execute transactions. Embedded in the Therapeutic Area Leadership Team to align external innovation with portfolio planning.

CSL

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.

Moderna London, United Kingdom

Hybrid Permanent

Associate Director, Computational Biology – Early Discovery

Lead a team of computational biologists to identify and validate novel oncology targets using integrated phenomics, transcriptomics, genomics, and proteomics data. Develop and scale methods for target discovery in oncology and immunological diseases, collaborating closely with biologists, data scientists, and engineers. Drive data strategy and present findings to stakeholders to advance drug discovery programs.

Recursion United Kingdom

On-site Permanent

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site Permanent

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

Senior Clinical Trial Manager, Cambridge, MA

The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent