Latest Genetic Engineering Jobs

Product Director, Evidence Preparation

Owns the product vision and roadmap for AI-enabled digital products that support structured, collaborative authoring of evidence and regulatory content across clinical, non-clinical, CMC, safety, regulatory and publications. Leads a multi-disciplinary product team, shapes scalable architecture with engineers, and drives an AI-first approach with GxP, privacy and AI governance embedded from the outset.

GSK London

Scientific Leader, Discovery Integration Sciences

Leads cross-functional teams designing, delivering and operating Lab-in-an-Automated-Loop systems that integrate computational intelligence with physical lab experimentation in adaptive learning cycles. Translates scientific requirements into system designs and platform capabilities, applying AI, agents and cloud-based workflow automation to accelerate medicine discovery. Hybrid role requiring on-site presence 2-3 days per week.

GSK USA - Pennsylvania - Upper Providence US$157,575 – US$262,625 pa

Hybrid

Warehouse Specialist, Logistics

Hands-on warehouse role at Moderna's Harwell mRNA manufacturing site, covering goods receipt, material picking, SAP inventory transactions, cycle counts and internal deliveries within a GMP/GDP environment. Works a fixed-shift pattern supporting 24/7 manufacturing, with scope to improve logistics workflows using digital tools such as SAP and Smartsheet.

Moderna Oxford

On-site Contract Shift-work Clearance Required

Principal Scientist, Immunogenicity and Ligand Binding Assays

Provides scientific and hands-on leadership for immunogenicity and ligand binding assay bioanalysis supporting mRNA-LNP therapeutic programs, spanning assay development, validation, clinical sample testing and regulatory submissions. Ensures GcLP compliance and partners with cross-functional teams, with opportunities to work alongside data and AI-enabled analytical approaches.

Moderna Oxford

Hybrid Permanent

Senior Director, Intl Regulatory Affairs Geo-Expansion

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

Vertex Pharmaceuticals London

Hybrid

Vertex Summer Intern, Commercial (10 weeks)

A 10-week summer internship within Vertex's Commercial Cystic Fibrosis team, supporting commercial strategy, marketing and patient access projects that drive awareness, uptake and access to CF therapies. Interns work alongside industry leaders, gaining hands-on exposure to rare disease commercialisation in a biopharmaceutical setting.

Vertex Pharmaceuticals London

Hybrid Internship

Medical Director Clinical Development- Aging

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging research. Leads a 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, regulatory and statistics partners.

GSK London US$189,750 – US$316,250 pa

Hybrid

Medical Director, Oncology Clinical Development - GU

Serves as the physician within an oncology clinical program team, leading medical monitoring and safety oversight for genitourinary cancer studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid working with at least two days per week on-site.

GSK Warsaw, Poland PLN 472,500 – PLN 787,500 pa

Hybrid

Medical Director, Oncology Clinical Development - GU

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator and KEE engagement, and regulatory interactions. May guide other physicians on complex multi-study programmes.

GSK Mississauga, Canada US$189,750 – US$316,250 pa

Hybrid

Medical Director-Oncology Clinical Development - GI

Serves as the physician within a clinical programme team, leading medical monitoring and safety oversight for oncology studies and interpreting clinical and safety data. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with a focus on GI oncology. Requires an on-site office presence two to three days a week.

GSK London US$222,750 – US$371,250 pa

Hybrid

Medical Director-Oncology Clinical Development - GI

Serves as the physician on a clinical programme team, leading medical monitoring and safety oversight for GI oncology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators and regulators. Works within a Clinical Matrix Team alongside Clinical Operations, Biostatistics, Regulatory and Pharmacovigilance, with on-site presence 2-3 days a week.

GSK Waltham, United States US$222,750 – US$371,250 pa

Hybrid

Medical Director-Oncology Clinical Development - GI

Serves as the physician within an oncology clinical programme team, leading medical monitoring, safety oversight and clinical data interpretation for GI studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires on-site presence 2-3 days a week, with the Stevenage base relocating to Cambridge, UK by early 2029.

GSK Stevenage US$222,750 – US$371,250 pa

On-site

Senior Medical Director, Oncology Clinical Development - Sarcoma

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves on the Clinical Matrix Team, mentors Medical Directors and engages external experts, with a minimum two days a week on-site presence.

GSK London US$284,250 – US$473,750 pa

On-site

Senior Medical Director, Oncology Clinical Development - Sarcoma

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Sits on the Clinical Matrix Team, mentors Medical Directors and engages external experts, KEEs and advisory boards. Requires deep soft tissue sarcoma and osteosarcoma drug development expertise.

GSK Waltham, United States US$284,250 – US$473,750 pa

On-site

Senior Medical Director, Oncology Clinical Development - Sarcoma

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, with a minimum two days a week on-site presence.

GSK Stevenage US$284,250 – US$473,750 pa

On-site