Latest IT Recruitment Jobs

Supported Studies Asset Study Delivery Lead - 14 month secondment

Leads end-to-end delivery of clinical study portfolios for a specific asset, coordinating proposal reviews for investigator-initiated and collaborative studies. Manages milestone tracking, budget forecasting, supply coordination, and stakeholder communication across cross-functional teams. Acts as primary operational contact and provides oversight in compliance with GCP and regulatory standards, while supporting team development and process improvements.

GSK United Kingdom

Contract

Product Owner, Clinical Trial Site Management

This role involves leading AI-first product development for clinical trial site management systems at GSK, focusing on transforming how trials are conducted through intelligent automation and data-driven decision-making. The Product Owner will own the strategy and delivery of scalable digital capabilities across feasibility, study start-up, contracting, and monitoring, ensuring adoption and compliance in a regulated GxP environment. Key responsibilities include driving innovation with AI-native solutions, aligning stakeholders, and embedding transformative technology into core operational workflows.

GSK United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis

Hybrid 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

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

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa

On-site Permanent

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

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading oncology clinical development for sarcoma, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, contribute to regulatory interactions, and mentor clinical teams, ensuring patient-centred strategies within a global matrix environment. Deep expertise in sarcoma oncology and cross-functional collaboration are central to the position.

GSK Stevenage, United Kingdom

Hybrid Permanent

Variation Planning Process Manager

The Variation Planning Process Manager will lead the design and implementation of Variation Planning processes within GSK’s ERP Evolution Programme, focusing on S/4HANA integration across Rx and Vx. The role involves defining end-to-end process frameworks, aligning with cross-functional teams including PLM, Quality, and Regulatory, and ensuring compliance with supply chain and regulatory requirements. Key responsibilities include process documentation, testing, change management, and transition planning from interim to future-state operations.

GSK €81,000 – €135,000 pa

Medical Director, Clinical Development, Hepatology

A Medical Director in Clinical Development for Hepatology will lead clinical strategy and execution for liver disease programs, contributing to clinical development plans, study design, and regulatory submissions. This role involves cross-functional collaboration, medical oversight of clinical trials, and integration of scientific and regulatory insights to advance GSK’s pipeline. The position plays a key part in driving transformative medicines from development through to approval, with a focus on scientific rigor and patient impact.

GSK United States

Medical Director, Clinical Development, Hepatology

A Medical Director in Clinical Development for Hepatology will lead clinical strategy and execution for liver disease assets, contributing to clinical development plans, study design, and regulatory submissions. The role involves cross-functional leadership, medical oversight of trials, and integration of scientific and clinical insights to advance drug development. It operates within a hybrid model, requiring on-site presence several days a week.

GSK US$222,750 – US$371,250 pa

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, ensuring operational strategy aligns with scientific goals and regulatory requirements. Oversees study delivery, vendor and resourcing strategy, risk management, and cross-functional coordination. Ensures inspection readiness and high-quality data output while leading matrixed teams and influencing senior stakeholders globally.

GSK United Kingdom

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, contribute to regulatory interactions, and mentor clinical teams within a matrixed global environment. The position requires deep expertise in oncology drug development and active engagement with external scientific leaders and regulatory authorities.

GSK United Kingdom

Hybrid Permanent

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize dose selection, trial design, and regulatory submissions. Work across multidisciplinary teams to drive quantitative decision-making in clinical pharmacology and contribute to the development of innovative cancer therapies.

GSK United States £188,100 – £313,500 pa

Director, Clinical Operations Asset Lead

This role 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. The individual will work closely with cross-functional teams to drive decision-making, manage vendor and resourcing strategies, and ensure compliance and inspection readiness. The position requires strategic leadership, strong stakeholder engagement, and deep expertise in global clinical development and regulatory environments.

GSK £189,750 – £316,250 pa

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