Latest Data Innovation Jobs

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

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

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

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

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

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, serving as the primary clinical accountability point on the Global Medicine Team. The leader designs and executes global clinical development plans, guides cross-functional teams through trial phases, and supports regulatory submissions and lifecycle strategies. Emphasis is placed on innovation, patient engagement, and strategic external collaboration to advance obesity and internal medicine therapeutics.

Pfizer

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and represent the programme externally at scientific forums. Based on-site in Waltham, MA, the position requires integration with cross-functional teams and mentorship of clinical staff to ensure patient-centred, scientifically rigorous drug development.

GSK £284,250 – £473,750 pa

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight and strategic input across study design, execution, and data interpretation. The position ensures patient safety and clinical integrity while guiding cross-functional teams and engaging with external experts. It requires deep expertise in oncology drug development and strong leadership in a matrixed global environment.

GSK US$284,250 – US$473,750 pa

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development strategy for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, mentor clinical teams, and represent the programme in regulatory and scientific forums. Based on-site at a GSK location with future relocation to Cambridge, UK.

GSK £284,250 – £473,750 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, ensuring patient safety and clinical integrity. The Medical Director provides physician-level input into study design, data interpretation, and regulatory interactions, working closely with cross-functional teams and external experts. It emphasizes integration of medical expertise across clinical development, with a focus on advancing cancer treatments through innovative science and collaboration.

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

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

This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. The Associate Medical Director will lead safety strategy, contribute to regulatory submissions, and guide cross-functional teams in pharmacovigilance activities. The position emphasizes evidence-based decision-making, global regulatory compliance, and proactive risk communication within a matrix environment.

GSK United States €87,000 – €145,000 pa

SERM Scientific Director

A senior scientific leadership role focused on pharmacovigilance and safety risk management for GSK's global pharmaceutical assets. The role involves leading safety strategy, evaluating clinical data, and ensuring regulatory compliance across development and post-marketing stages. It requires deep expertise in drug safety, cross-functional leadership, and communication with regulatory authorities.

GSK PLN 419,250 – PLN 698,750 pa

Director, Oncology Translational Medicine Project Manager

This role involves managing and overseeing translational research alliances, regulatory submissions, and diagnostic target profiles for GSK's Oncology portfolio. The Director will coordinate with internal and external stakeholders to ensure high-quality data and documentation, manage risks, and support the OTM Leadership Team.

GSK

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

This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK's clinical and post-marketing assets. The Associate Medical Director will lead signal detection, contribute to pharmacovigilance strategy, and ensure robust safety oversight across global development programs. Working within a cross-functional matrix, the role emphasizes evidence-based decision-making, regulatory compliance, and proactive risk communication to protect patient safety.

GSK Manchester, M4 6AL, United Kingdom €87,000 – €145,000 pa

Hybrid Permanent