Latest Genetic Engineering Jobs

Director, Real World Data Strategy and External Partnerships Lead

Leads the strategic execution of external Real World Data partnerships to support R&D and portfolio decision-making, working with clinical, medical and RWE leaders to assess scientific value. Stewards investment governance, manages a portfolio of RWD and external cohorts, and partners with legal, procurement, data platforms and AI engineering teams to ensure research-ready, compliant data products.

GSK London

Principal Scientist (m/f/d) Genomic Technologies, Human Genetics and Genomics

Join GSK's Genomic Technologies team within Translational Sciences, working alongside statistical geneticists to analyse large-scale human genetic data from biobanks such as UK Biobank and All of Us. The role involves developing and testing production methods for genetic analysis, integrating multi-omic and phenotypic data to identify causal genes and drug targets, and collaborating with Data and Predictive Sciences, Biostatistics, AI/ML and disease area teams to inform portfolio decisions.

GSK Heidelberg, Germany €74,250 – €202,125 pa

On-site

Analyst, Quality Control, Microbiology

Perform routine environmental monitoring and critical utility sampling, plus water testing for TOC, conductivity, bioburden and endotoxin in a GMP manufacturing facility. Execute QC microbiology methods including sterility, bioburden and endotoxin testing, support method transfers and qualifications, and author quality records such as deviations, CAPAs and SOPs.

Moderna Quality

On-site Permanent Clearance Required

Principal Scientist, Immunogenicity and Ligand Binding Assays

Provides scientific and hands-on oversight of ligand binding assay bioanalysis and immunogenicity testing for mRNA-LNP therapeutic programs, leading ADA and neutralizing antibody assay development, validation and clinical sample testing. Ensures GcLP compliance, reviews analytical data and supports regulatory submissions within cross-functional clinical development teams.

Moderna Clinical Development

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Lung

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across lung cancer studies within a clinical programme team. Partners with the Senior Scientist and cross-functional groups on protocol design, regulatory interactions and external scientific engagement, while mentoring Medical Directors. Requires an on-site presence at least two days a week.

GSK London US$242,550 – US$404,250 pa

On-site

SERM Medical Director, Oncology

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and interacts with regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK London

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development, interpreting safety data, escalating signals and delivering evidence-based benefit-risk recommendations. Leads Safety Review Teams and cross-functional matrix groups, representing Safety to governance committees and regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK Poznań, Poland £410,250 – £683,750 pa

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership in pharmacovigilance and risk management for oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering evidence-based benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and Safety Review Teams, and presents to senior governance committees and regulators. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK Wavre, Belgium

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering evidence-based benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and may lead Safety Review Teams. The role is hybrid across the UK, Belgium, Poland or Italy, with on-site attendance for key meetings.

GSK Siena, Italy £81,750 – £136,250 pa

Hybrid

Clinical Development Senior Medical Director - Cardiovascular

Leads clinical development medical activities for cardiovascular and vascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, leads the clinical matrix team, and engages with regulators, KOLs and cross-functional partners in a hybrid working model.

GSK Stevenage US$284,625 – US$474,375 pa

Hybrid

VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability and chairing a cross-functional matrix Medicine Development Team spanning clinical, translational, regulatory, manufacturing and commercial. Drives strategy, go/no-go decisions and lifecycle plans for novel vaccine platforms such as mRNA and neoantigen-based therapies.

GSK London US$340,500 – US$567,500 pa

Hybrid

VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability across major markets. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology/biomarkers, manufacturing, regulatory, safety, medical affairs and commercial, and represents the asset to senior governance boards.

GSK Waltham, United States US$340,500 – US$567,500 pa

Hybrid

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance. Works with the Global Regulatory Lead and cross-functional teams to shape development plans and support submissions and interactions with regulatory authorities across multiple regions.

GSK Stevenage €98,250 – €163,750 pa

Hybrid

VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and leads a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and sets the asset strategy within GSK's oncology R&D portfolio.

GSK Stevenage US$340,500 – US$567,500 pa

Hybrid

VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability across major markets. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology/biomarkers, manufacturing, regulatory, safety, medical affairs and commercial, and serves as asset spokesperson to senior governance boards.

GSK Zug, Switzerland US$340,500 – US$567,500 pa

Hybrid