Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director · manages people

Provides clinical and scientific leadership across cardiovascular clinical development programs, designing CDPs, study protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, partners with biology, translational sciences, regulatory and commercial groups, and serves as clinical point of contact for regulators, investigators and key experts. Hybrid role with at least two on-site days per week.

• Waltham, United States
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, and regulatory partners.

• 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.

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• United Kingdom
• Remote
• Director · manages people

Senior physician role leading medical science and strategy for oncology across a clinical research business, shaping RFP responses, bid defences and protocol design while engaging client medical leadership. Also provides therapeutic training, mentoring and regulatory document input, working in a matrixed global team with international travel.

• Oxford
• On-site
• Entry level

Postdoctoral researchers join an interdisciplinary team fabricating three-dimensional living, synthetic and hybrid tissues for disease modelling, therapeutic testing and organ repair. Openings span cell biology, electrophysiology, bioinformatics, hydrogel science and tissue engineering, combining stem cell biology, bioprinting and device engineering within a group of about 15 members.

Multielectrode Arrays · Calcium Imaging · Optogenetics +4

• Oxford
• On-site
• Entry level
• Permanent

Design and conduct experiments on nanopore technologies, single-molecule analysis, and 3D tissue engineering, spanning chemistry, biology, physics and engineering. Postdocs lead development of emerging biotech methods, publish impactful research, and mentor junior researchers within a 100+ researcher institute.

3D Printing

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Experienced medicinal chemists lead portfolio drug discovery projects from initiation to clinical candidate selection, working as Project Lead or Medicinal Chemistry Lead. They partner closely with ML scientists to refine the AI drug design platform, manage CRO resources, and may line-manage teams of 2-4 chemists.

AlphaFold

• Cambridge, United States
• Hybrid · 3 days in office
• Lead

Lead DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating DMPK, PD and toxicology data for dose and safety predictions. Work closely with AI/ML platform teams to optimise computational ADME models and author regulatory sections, in a hybrid Cambridge, MA role.

Python · R

• London
• On-site
• Mid-level
• Permanent

Own the full post-training lifecycle for biological foundation models, from alignment strategy to production deployment. Design pipelines that adapt general-purpose models to therapeutic contexts, build validation frameworks linking model improvements to biological ground truth, and run experiments end-to-end on distributed GPU infrastructure. Collaborate with ML infrastructure and biology teams and contribute to open-source tooling.

OpenTargets · helical-package · GPU

• 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.

• Oxford
• On-site
• Entry level
• Temporary

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

GraphPad Prism · LIMS · Word +2

• Uxbridge
• Director

Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.

• Oxford
• Lead · manages people

Lead a team of scientists developing novel biologic therapies for autoimmune disease, overseeing in vitro and in vivo pharmacology studies for lead and early discovery programs. Collaborate across immunology, protein engineering, translational medicine and biomarkers to deliver data packages for progression to development, while mentoring staff and contributing to INDs and patents.

• High Wycombe
• Hybrid
• Mid-level

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving risk monitoring reviews, advising on CAPA plans, and leading pre-submission quality portfolio reviews and mock inspections. Combines hands-on risk ownership with cross-functional influence and coaching of team members.

Microsoft Office · Tableau · Spotfire