Latest regulatory affairs Jobs

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities within global oncology R&D, focusing on study design, protocol development, and clinical data review across the development lifecycle. The individual will act as a subject matter expert, ensuring scientific rigor and regulatory compliance while collaborating with cross-functional teams and external partners. A key focus is on immuno-oncology, with responsibilities spanning from early-phase to late-stage clinical development.

GSK

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for Internal Medicine assets within Pfizer's R&D organization, with end-to-end accountability for creating and executing global clinical development plans. Serves as the primary clinical point of contact across cross-functional teams and external partners, driving trial design, regulatory submissions, and lifecycle strategy. Focuses on obesity and related therapeutic areas, integrating innovation, patient engagement, and regulatory expertise to advance drug development.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for assigned internal medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. Oversees cross-functional teams to design and deliver clinical trials supporting regulatory submissions, while providing therapeutic expertise in obesity and endocrinology. Engages external stakeholders and contributes to regulatory strategy, safety reporting, and product labeling.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Precision Medicine Director

Leads the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives to support patient selection and regulatory submissions in neuroscience. Acts as a scientific expert, leading cross-functional teams and ensuring compliance with medical device regulations. Facilitates collaborations with external research partners and drives operational excellence in biomarker strategy implementation.

Novartis

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

This role involves hands-on laboratory work supporting immunoassay development and clinical testing for Moderna’s mRNA-based therapeutic programs. The technician will prepare reagents, conduct sample analysis, ensure regulatory compliance, and contribute to high-quality data generation for clinical trials. Based in Oxford, the position requires full-time on-site work in a regulated lab environment with occasional overtime.

Moderna Oxford, United Kingdom

On-site Contract

QC Analytical Scientist

The role involves performing analytical testing in a GMP-compliant laboratory environment, including in-process and release testing of drug products using techniques such as ddPCR, flow cytometry, sterility testing, and endotoxin assays. The scientist ensures data integrity, supports method validation and tech transfer, investigates quality events, and maintains laboratory compliance. This is a shift-based position requiring hands-on work with cell-based therapies in a regulated, cleanroom setting.

Autolus Stevenage, United Kingdom

On-site Permanent Shift-work

Bioanalytical Lead, London

Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

(Senior) Group Leader, Plant Phenotyping - Plant Biology Institute

Leads a transformative research programme in next-generation plant phenotyping, developing automated, high-throughput, sensor-based technologies to measure plant performance across indoor and outdoor environments. Builds and manages an interdisciplinary team spanning biology, engineering, data science, and automation, while establishing pipelines for processing and analysing phenotyping data. Collaborates with AI and ML experts to accelerate discovery and translate research into commercially relevant, sustainable agricultural solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

(Senior) Group Leader, Nitrogen Fixation - Plant Biology Institute

Lead a flagship research programme in biological nitrogen fixation, focusing on engineering novel nitrogen-fixing systems in plants using metabolic and protein engineering. Recruit and manage a high-performing research team, drive translational science from lab to field, and collaborate across EIT’s interdisciplinary ecosystem. The role emphasizes rigorous experimental design, stage-gated research delivery, and the development of commercially viable, impact-driven plant science solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent