Latest Genetic Engineering Jobs

Director, Real World Data Platform and Portfolio Lead

Leads strategic execution of internal and external real-world data platform partnerships to support R&D and portfolio decision-making, spanning multiple geographies and health systems. Coordinates data acquisition, governance, linkage and evidence generation with engineering, AI, DevOps and therapy-area teams, and maintains the RWD asset inventory and partnership KPIs.

GSK London

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, aligning data acquisition with pipeline strategy across therapy areas. Acts as Business Data Owner for RWD assets, stewarding investment governance, data quality and compliance, and working with legal, procurement, data platforms and AI engineering teams to deliver research-ready, FAIR data products.

GSK USA - Pennsylvania - Upper Providence

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

Lead the development, qualification, validation and execution of complex cell-based immunoassays generating high-quality data for clinical trials across multiple therapeutic areas. Act as scientific point of contact within the Immuno-assays group, collaborating with multidisciplinary teams and external partners, and coaching junior laboratory staff.

Moderna Clinical Development

Hybrid Permanent

(Fixed Term) Manufacturing Associate I

Operate production equipment in an mRNA vaccines unit, following cGMP, safety and gowning procedures while executing manufacturing documentation. Partner with QA on batch disposition, lead RCA and CAPA investigations, and troubleshoot routine equipment and digital issues. Site-based role with basic mechanical maintenance and continuous improvement work in a fast-paced, cross-functional team.

Moderna Drug Manufacturing

On-site Temporary Clearance Required

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 closely with the Global Regulatory Lead and cross-functional teams to align regulatory plans with development strategy and support authority interactions and submissions across multiple regions.

GSK London €98,250 – €163,750 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 authority interactions and submissions across multiple regions.

GSK Wavre, Belgium €98,250 – €163,750 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. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

GSK Waltham, United States US$284,625 – US$474,375 pa

Hybrid

Clinical Development Senior Medical Director - Cardiovascular

Leads clinical development medical activities for cardiovascular and vascular programs across early and late-phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

GSK London US$284,625 – US$474,375 pa

Hybrid

Clinical Development Medical Director - Cardiovascular

Provides clinical and scientific leadership across cardiovascular clinical development programmes, shaping study designs, translational plans and regulatory documents within the Respiratory, Immunology & Inflammation Research Unit. Leads a Clinical Matrix Team, oversees participant safety and medical monitoring, and works cross-functionally with biology, regulatory, statistics and commercial partners. Hybrid working with at least two days per week on-site.

GSK London US$222,750 – US$371,250 pa

Hybrid

Clinical Development Medical Director - Cardiovascular

Leads clinical development strategy for cardiovascular assets within the Respiratory, Immunology & Inflammation Research Unit, designing clinical development plans, protocols and regulatory documents while providing medical monitoring and safety oversight. Chairs the Clinical Matrix Team and serves as primary clinical contact for regulators, investigators and key external experts across early and late-stage programs.

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

Hybrid

Clinical Development Medical Director - Cardiovascular

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

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

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators. Hybrid UK-based role with mentoring and process-improvement duties.

GSK London

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and may lead Safety Review Teams. Hybrid role based in the UK with global regulatory and partner interaction.

GSK Wavre, Belgium

Hybrid

Interventional Study Scientist Medical Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

GSK London US$187,275 – US$312,125 pa

Hybrid

Interventional Study Scientist Medical Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

GSK Waltham, United States US$187,275 – US$312,125 pa

Hybrid