Latest Biotech Research Scientist Jobs

Director, Search & Evaluation Early TA Lead (CVR and Haem)

Leads strategic sourcing and evaluation of early-stage external innovation in Hematology or Cardiovascular/Renal therapeutic areas. Identifies and advances preclinical to Phase 1 assets, drives due diligence, and shapes partnering strategies within cross-functional teams. Represents the therapeutic area externally, building relationships with biotech, academia, and investors to strengthen the innovation pipeline.

CSL

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna

On-site Permanent

Senior Computational Biologist - Early Discovery Oncology

Drive target discovery and validation in precision oncology by integrating multimodal biological data (phenomics, transcriptomics, genomics, proteomics) to identify novel therapeutic targets. Collaborate with cross-functional teams to develop scalable computational methods and build compelling data packages that advance drug programs. Develop criteria for target nomination and support early translational strategies using AI-powered platforms.

Recursion United Kingdom £151,800 – £220,660 pa

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

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Leads the strategic planning and management of FSP (Functional Service Provider) resources within Clinical Operations, ensuring optimal resourcing, vendor performance, and cost efficiency across clinical trial functions. Acts as the primary liaison between Clinical Operations and FSP vendors, driving data-informed workforce models, financial oversight, and compliance. Works closely with Procurement/Outsourcing Excellence to align vendor contracts and governance with operational needs while supporting audit readiness and process improvement.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent

Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Moderna

Hybrid 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

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing studies and guiding regulatory submissions. Oversee modeling and simulation to inform dose selection and accelerate drug development. Collaborate across translational, clinical, and preclinical teams in a tech-driven biopharma environment.

Recursion United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Leads end-to-end management of FSP (Functional Service Provider) resources within Clinical Operations, including workforce planning, vendor oversight, and financial control. Acts as the primary liaison between Clinical Operations and FSP vendors, ensuring resourcing strategies align with study demands and organizational frameworks. Develops data-driven forecasting models and dashboards to optimize capacity, cost, and performance across global clinical trials.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent