Latest Data Innovation Jobs

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

Director, Oncology Translational Medicine Project Manager

This role involves managing and coordinating translational research alliances and collaborations, regulatory submissions, and diagnostic target profiles for GSK's Oncology portfolio. The Director will oversee project plans, track milestones, manage risks, and ensure high-quality data packages are delivered to support oncology asset development and approvals.

GSK United States

Director, Oncology Translational Medicine Project Manager

This role involves managing and coordinating translational research alliances and collaborations, regulatory submissions, and diagnostic target profiles for GSK's Oncology portfolio. The Director will oversee external partnerships, track project milestones, and ensure high-quality data packages are delivered to support oncology asset development and approvals.

GSK

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

Provides medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. Key responsibilities include signal detection, safety oversight, regulatory reporting, and contributing to global pharmacovigilance strategy. Works cross-functionally to ensure patient safety and compliance with international regulations.

GSK €87,000 – €145,000 pa

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves providing medical and scientific leadership in the safety evaluation and risk management of GSK’s clinical and post-marketing pharmaceutical assets. The Associate Medical Director will lead signal detection, benefit-risk assessment, and pharmacovigilance strategy, ensuring robust safety oversight across global development programs. Working within a cross-functional matrix, the individual will influence safety governance, contribute to regulatory submissions, and drive evidence-based decisions to protect patient safety.

GSK €87,000 – €145,000 pa

Hybrid Permanent

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 Quality Strategy Leader

This role involves setting and governing end-to-end product quality strategy for business-critical assets, ensuring alignment across multiple functions and stakeholders. Responsibilities include leading product quality teams, representing quality in governance forums, and managing product quality risk throughout the lifecycle from development to commercialization.

GSK East Hertfordshire, United Kingdom

Product Quality Strategy Leader

This role involves leading the development and integration of end-to-end product quality strategies for critical pharmaceutical assets, ensuring alignment across multiple functions and stakeholders. Responsibilities include risk management, regulatory compliance, and strategic input for product launch and lifecycle activities.

GSK Barnard Castle, United Kingdom

Product Quality Strategy Leader

The Product Quality Strategy Director is responsible for setting and governing end-to-end product quality strategies for business-critical assets, ensuring alignment across multiple functions and stakeholders. Key activities include leading product quality teams, representing quality in governance forums, and managing product quality risks throughout the lifecycle from development to commercialization.

GSK

Product Quality Strategy Leader

The Product Quality Strategy Director is responsible for setting and governing end-to-end product quality strategies for business-critical assets, ensuring alignment across various functions and stakeholders. Key responsibilities include leading the Product Quality Team, representing Quality in governance forums, and driving proactive risk management and continuous improvement.

GSK

Director, Biostatistics

Lead statistical strategy for clinical development projects in inflammation and immunology, providing expert input on study design, analysis plans, and regulatory submissions. Collaborate with cross-functional teams to ensure robust data interpretation and compliance with global standards. Drive innovation in statistical methodology and support publication activities and product defense.

Pfizer Marlow, United Kingdom

Director, Biostatistics

Leads statistical strategy and oversight for global clinical development projects in inflammation, immunology, and specialty care. Provides expert input on study design, analysis plans, and regulatory submissions while guiding cross-functional teams and external collaborators. Focuses on innovation in statistical methodology and ensures compliance with regulatory standards and internal processes.

Pfizer Cambridge, United Kingdom

Director, Biostatistics

Leads statistical strategy and execution for global clinical development projects in inflammation, immunology, and specialty care. Provides expert input on study design, analysis plans, and regulatory submissions while advancing innovative methodologies. Collaborates across functions to ensure high-quality, compliant statistical deliverables and supports publication and product defense activities.

Pfizer Sandwich, United Kingdom

Director, Biostatistics

Leads statistical strategy for global clinical development in inflammation, immunology, and specialty care, providing oversight on study design, analysis, and regulatory submissions. Manages cross-functional collaboration and drives innovation in statistical methodology. Works closely with clinical, regulatory, and data teams to ensure high-quality, compliant deliverables across the drug development lifecycle.

Pfizer United Kingdom