Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid
• Director

Senior individual-contributor role building a cardiovascular and cardiometabolic translational biology strategy within a respiratory and immunology research unit. Involves defining human-relevant mechanistic hypotheses, biomarker strategies, target evaluation, and business development diligence, with influence across four disease areas in a matrixed organisation.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Owns the clinical strategy, scientific narrative and benefit-risk framework for genitourinary cancer assets, acting as the senior clinical authority on the Medicine Development Team core quad. Sets asset-level evidence-generation and governance direction while Senior Scientists handle study-level delivery, and represents Clinical Development in health authority and external engagements. Hybrid role with at least two on-site days per week.

AI · Advanced Analytics

• Reading
• Mid-level

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, with a focus on oncology studies. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team partnering with smaller emerging biopharma companies.

Trial Master File · Investigator's Site File

• London
• Remote
• Freelance

Supports UK clinical trial start-up by collecting and reviewing site and regulatory documentation, preparing submission packages, and coordinating Informed Consent Form adaptations. Liaises with investigative sites and internal study teams to resolve outstanding documents and track progress against milestones, ensuring ICH-GCP and local regulatory compliance.

• Oxford
• On-site
• Mid-level

Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.

Emerson DeltaV · Allen-Bradley · Rockwell Automation +7

• Oxford
• On-site
• Mid-level

Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.

LabVantage · LIMS · Generative AI

• Woking
• On-site
• Senior

Owns the product and go-to-market strategy for Digital CMC at IDBS, identifying high-value opportunities to digitise CMC development, submission readiness, technology transfer and lifecycle management. Translates real-world CMC problems into business cases and roadmap priorities, applying structured scientific data, workflow automation and agentic AI. Market-facing role reporting to the Director, Strategic Operations, partnering with biopharma customers and cross-functional teams.

ELN · LIMS · MES +7

• Newcastle upon Tyne
• On-site
• Senior

Provides advanced third-level technical support for Digital Pathology products including the Aperio GT Platform, CytoVision and CytoInsight, resolving complex escalations and communicating guidance to field teams. Owns service readiness for change requests and new product development, partnering with R&D, Quality and Product Management to turn findings into documented defects and service improvements.

Aperio GT Platform · Aperio FL · CytoVision +7

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Accountable for end-to-end clinical development strategy for an antibody-drug conjugate asset across multiple tumour types, from first-in-human through registrational trials and launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial.

• Upper Providence
• Hybrid · 2–3 days in office
• Director · manages people

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, approval and launch. Sets disease-area strategy, chairs governance forums and advisory boards, and line-manages clinical development leads within a global matrix. Distinct for its portfolio-level enterprise scope and hybrid US/UK/Swiss base.

AI/ML

• Baar Onyx
• Hybrid · 2–3 days in office
• Director · manages people

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, regulatory approval and initial launch. Chairs governance forums, co-leads matrix asset teams and line-manages clinical development leads, medical directors and clinical scientists. Distinct for its portfolio-level scope across early- and late-phase programs and its cross-functional connector role spanning research, translational medicine and commercial strategy.

AI/ML

• London
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across early and late-stage respiratory development programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and partners with biology, translational sciences, regulatory and commercial colleagues. Distinct for its focus on pulmonary hypertension and translational biomarker work within GSK's Respiratory, Immunology & Inflammation Research Unit.

• Waltham, United States
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across respiratory and immunology clinical development programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and acts as the clinical point of contact for regulators, investigators and key external experts. Hybrid working with at least two days per week on-site.

• Stevenage
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across early and late-stage respiratory programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and partners with biology, regulatory, commercial and statistics groups to advance differentiated medicines.

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

Provides clinical and scientific leadership across early and late-stage respiratory programs, designing clinical development plans, protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, shaping translational strategy, target validation and evidence generation in partnership with biology, regulatory and commercial groups.