Latest Biotech Research Scientist Jobs

Principal Programmer Analyst

This role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, fostering quality assurance, and collaborating with cross-functional teams to bridge scientific requirements with technical solutions.

GSK USA - Pennsylvania - Upper Providence

Principal Programmer Analyst

The Principal Programmer Analyst role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, supporting regulatory interactions, and implementing innovative solutions to improve efficiency and compliance.

GSK London, Greater London, United Kingdom

Hybrid Permanent

Executive Director, Clinical Pharmacology/Pharmacometrics

This role involves leading clinical pharmacology and pharmacometrics strategies for rare disease and oncology programs, designing clinical studies, and interfacing with regulatory authorities. The position requires extensive experience in drug development, proficiency with modeling software, and collaboration with cross-functional teams.

Recursion Remote Opportunity - United Kingdom

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 Salt Lake City, Salt Lake County, United States

On-site Permanent

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, Greater London, United Kingdom

On-site Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.

Moderna Oxford, Oxfordshire, United Kingdom

Hybrid Permanent

Data Solution Architect

The Data Solution Architect designs end-to-end data solutions, including data integration, warehousing, governance, and analytics. They work closely with technical leads and data teams to ensure scalable, secure, and governed solutions, influencing the data architecture of a rapidly evolving biotech company.

Autolus London, Greater London, United Kingdom

Regulatory Strategy Manager

The Regulatory Strategy Senior Manager leads the development and implementation of regulatory strategies for assigned regions, ensuring compliance with health authority requirements. They provide strategic input for product development, manage regulatory submissions, and contribute to global regulatory strategy.

Vertex Pharmaceuticals London, Greater London, United Kingdom

Regulatory Submissions Ass Manager II

This role involves managing regulatory submissions for clinical trials, ensuring compliance with EU Clinical Trial Regulation (CTR) and CTIS operations. Responsibilities include preparing and submitting applications, coordinating with regulatory authorities, and mentoring junior team members.

Fortrea Leeds, West Yorkshire, United Kingdom

Executive Director / Vice President, Business Development

Lead business development strategy to identify and execute strategic partnerships, in- and out-licensing deals, co-developments, and M&A opportunities in oncology and autoimmune disease. Represent Autolus at high-level meetings, build relationships across biotech, pharma, and academia, and collaborate with cross-functional teams to align BD initiatives with corporate goals. Requires deep expertise in biopharma deal-making and strong scientific-business acumen.

Autolus US - East Coast

R&D Consultant - Drug Delivery Device Design - Cambridge

This role involves leading the design and development of next-generation drug delivery devices, guiding multidisciplinary teams, and driving R&D activities. Responsibilities include concept generation, prototyping, experimental design, and risk management, with a focus on translating technical challenges into actionable development strategies.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

Programme/Project Manager

This role involves building and running an integrated delivery plan for a major pharma partnership, coordinating multidisciplinary teams, and ensuring smooth project execution. Responsibilities include setting milestones, managing risks, and maintaining stakeholder alignment.

Genomics London, Greater London, United Kingdom

Hybrid Permanent

Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)

This role involves developing and maintaining labeling strategies for pharmaceutical products, including the creation and management of core data sheets, US Prescribing Information, and EU Summary of Product Characteristics. The Senior Consultant will collaborate with various stakeholders to ensure global alignment and compliance, and contribute to clinical study designs and regulatory strategies.

Parexel Harrow, Greater London, United Kingdom

Remote

Snr Data Scientist, Computational Genomics/DNA Modelling

This role involves developing and applying machine learning models to connect genetic variation and regulatory DNA sequences to downstream molecular phenotypes and disease biology. You will work closely with experimental and machine learning researchers to validate hypotheses and guide downstream studies, contributing to scientific excellence and external visibility.

Relation Therapeutics London, Greater London, United Kingdom

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 Cambridge, Middlesex County, United States

Hybrid Permanent