Latest Recruitment Jobs

External Manufacturing DS Supply Director

Leads external manufacturing relationships with contract manufacturing organizations (CMOs) to ensure reliable supply of medicines and vaccines. Oversees performance metrics, strategic alignment, and operational execution across complex supply chains. Provides leadership to teams and integrates new products into the commercial portfolio while maintaining quality and compliance.

GSK

On-site Permanent

Principal Programmer Analyst

The Principal Programmer Analyst role involves leading statistical programming activities for clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, working in an agile, squad-based environment.

GSK Stevenage, United Kingdom

Executive Director, Chemical Biology/Drug Design

This role involves leading chemical biology efforts to bridge multiomic discovery with target identification, managing a team of designers, and driving programs that integrate computational and generative design approaches. The role focuses on developing new modalities like targeted protein degradation and molecular glues, working closely with biology, data science, and computational teams.

Recursion United Kingdom £237,600 – £284,900 pa

Don't see what you're looking for?

This is a general talent network sign-up opportunity rather than a specific job role. Candidates can submit their resume for future consideration at Recursion, a clinical-stage TechBio company using AI and automated biology to accelerate drug discovery. The company emphasizes bold, ethical innovation and cross-functional collaboration to address unmet medical needs.

Recursion United Kingdom

On-site Permanent

Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

Global Site and Study Operations Undergraduate

This role involves hands-on experience in clinical trial execution, regulatory documentation, and site operations. The candidate will work closely with experienced managers and teams, gaining insights into multiple therapeutic areas and contributing to process improvements.

Pfizer Sandwich, United Kingdom

Executive Director / Vice President, Business Development

Lead business development strategy to identify and execute strategic partnerships, in- and out-licensing deals, co-developments, and M&A opportunities in oncology and autoimmune disease. Represent Autolus at high-level meetings, build relationships across biotech, pharma, and academia, and collaborate with cross-functional teams to align BD initiatives with corporate goals. Requires deep expertise in biopharma deal-making and strong scientific-business acumen.

Autolus

Director, Clinical Operations Asset Lead

The Clinical Operations Asset Lead is responsible for the strategic and operational delivery of clinical trials across the full asset lifecycle. This role involves leading cross-functional teams, ensuring high-quality data, and driving innovative approaches to clinical research.

GSK

Director, Clinical Operations Asset Lead

Leads clinical operations strategy across the full asset lifecycle, ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to shape clinical development plans, manage vendor and resourcing strategies, and maintain inspection readiness. Focuses on patient-centric, efficient study execution within a global, matrixed environment.

GSK

Director, Clinical Operations Asset Lead

Leads clinical operations strategy and execution across the full lifecycle of a drug development asset, ensuring high-quality, compliant, and efficient delivery of global clinical trials. Works cross-functionally to shape development plans, manage risk, and align operational delivery with scientific and regulatory goals. Provides strategic leadership to study teams and represents clinical operations at senior governance levels.

GSK

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study execution with scientific and regulatory goals, driving innovation and efficiency while managing risks and stakeholder engagement. Serves as the primary accountability point for clinical operations within global governance structures.

GSK €119,250 – €198,750 pa

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study design with strategic goals, manage vendor and resourcing strategy, and maintain inspection readiness. Serves as the primary escalation point for operational and quality issues, driving governance and risk management.

GSK

Hybrid Permanent

Director, Clinical Operations Asset Lead

The Clinical Operations Asset Lead is responsible for the strategic and operational delivery of clinical trials across the full asset lifecycle. This role involves setting and executing the program-level operational strategy, leading cross-functional teams, and ensuring high-quality, on-time delivery of clinical studies.

GSK £189,750 – £316,250 pa

Director, Quantitative Systems Pharmacology

This role involves leading the development and application of quantitative systems pharmacology (QSP) models to enhance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.

GSK United States

Director, Quantitative Systems Pharmacology

This role involves leading the development and application of quantitative systems pharmacology models to enhance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.

GSK

Hybrid Permanent