Latest Analytical Instruments Jobs

Director, Clinical Science – Oncology Clinical Development

Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory deliverables within a global pharmaceutical environment. Collaborate across functions to ensure scientific rigor and alignment with clinical development goals, while engaging with external experts and supporting regulatory submissions. The role emphasizes innovation, data-driven decision-making, and continuous improvement in clinical development processes.

GSK £189,750 – £316,250 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with clinical strategy, while supporting the execution of clinical studies from early to late stages. Focuses on generating robust clinical insights to advance cancer therapies with high unmet need.

GSK United States £189,750 – £316,250 pa

Hybrid Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.

Moderna

Hybrid Permanent

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing to support GMP quality control for mRNA products. The analyst will execute tests including sterility, bioburden, endotoxin, and TOC, while supporting method transfers, validations, and compliance with cGMP standards. The position requires strong documentation practices, collaboration with cross-functional teams, and active participation in quality systems such as investigations and audits.

Moderna

On-site Permanent

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership in oncology clinical development, specifically for genitourinary (GU) cancers. The Medical Director will lead medical monitoring, contribute to protocol design, interpret clinical data, and ensure patient safety across clinical trials. They will work closely with cross-functional teams, engage with external experts, and support regulatory submissions and scientific communications within a global pharmaceutical environment.

GSK

Hybrid Permanent

Medical Director-Oncology Clinical Development - GI

This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.

GSK United Kingdom £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.

GSK £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.

GSK

Hybrid Permanent

Head, Oncology Clinical Development - ADCs

Lead the clinical development strategy for antibody-drug conjugates (ADCs) across multiple tumor types, from early-phase through registrational trials and market launch. Drive integrated clinical and translational research, represent the asset at key governance forums, and shape portfolio-level decision-making in oncology. Work across global cross-functional teams to advance innovative therapies within a matrixed biopharma environment.

GSK United States £242,250 – £403,750 pa

Head, Oncology Clinical Development - ADCs

Leads the end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and launch readiness. Responsible for shaping clinical strategy, overseeing global trials, engaging with regulatory authorities, and leading cross-functional teams in a matrixed environment. Involves governance leadership, scientific advisory boards, and integration of innovative approaches such as AI/ML and real-world evidence to accelerate development.

GSK US$242,250 – US$403,750 pa

Head, Oncology Clinical Development - ADCs

Leads the clinical development strategy for antibody-drug conjugates (ADCs) in oncology, spanning early- to late-phase trials across multiple tumor types. Responsible for end-to-end asset development, including regulatory approval and launch readiness, with a focus on scientific rigor, innovation in trial design, and cross-functional collaboration. Engages with global health authorities, governance bodies, and external experts to shape clinical and translational strategies.

GSK US$242,250 – US$403,750 pa

Head, Oncology Clinical Development - ADCs

Leads end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and market launch. Drives integrated clinical strategy, translational research, regulatory submissions, and cross-functional collaboration across global teams. Engages with governance bodies, scientific advisory boards, and external experts to shape development and competitive positioning.

GSK US$242,250 – US$403,750 pa

Medical Director, Oncology Clinical Development - Hematology

The Medical Director, Oncology Clinical Development - Hematology is a physician-led role focused on guiding clinical strategy and medical oversight in oncology drug development. This position involves leading medical monitoring, interpreting clinical and safety data, contributing to protocol design, and engaging with investigators and regulatory bodies. The role operates within cross-functional teams to ensure patient safety and clinical integrity across Phase I–III trials in hematology and oncology.

GSK United States

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It emphasizes physician leadership in trials from Phase I–III, with a strong focus on real-world impact and regulatory engagement.

GSK £222,750 – £371,250 pa

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight and clinical development for oncology and hematology programs, with responsibilities spanning study design, safety monitoring, data interpretation, and regulatory engagement. The Medical Director will collaborate with cross-functional teams and external experts to ensure clinical integrity and patient-centered decision-making in late-stage drug development. The position requires deep expertise in hematology-oncology and experience in Phase I–III trials within a pharmaceutical or biotech setting.

GSK PLN 455,250 – PLN 758,750 pa