Biotechnology Jobs

Safety Scientist – SERM (Safety Evaluation and Risk Management)

A Safety Scientist in GSK's Safety Evaluation and Risk Management (SERM) team leads signal detection, safety evaluations, and risk management for pharmaceutical products in clinical development and post-marketing. The role involves authoring regulatory safety documents, contributing to Risk Management Plans, and collaborating with cross-functional teams to ensure patient safety. It requires strong scientific judgment, pharmacovigilance expertise, and the ability to communicate safety risks effectively across global teams.

GSK

Hybrid Permanent

Safety Scientist – SERM (Safety Evaluation and Risk Management)

A Safety Scientist in GSK's Safety Evaluation and Risk Management (SERM) team leads signal detection, safety evaluations, and risk management for pharmaceutical products across clinical and post-marketing stages. The role involves authoring regulatory safety documents, contributing to Risk Management Plans, and collaborating with cross-functional teams to ensure global patient safety. It emphasizes scientific rigor, data interpretation, and proactive risk communication within a matrix environment.

GSK United Kingdom PLN 215,250 – PLN 358,750 pa

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

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

Postdoctoral Research Scientists - Materials & Devices for Life Sciences

This role involves advancing interdisciplinary research in materials and devices for life sciences, focusing on nanopore technologies, 3D tissue engineering, and device development for clinical diagnostics and therapeutics. The scientist will design experiments, refine emerging technologies, and contribute to high-impact publications in a collaborative, well-resourced environment. Work spans molecular sciences, nanotechnology, and bioengineering to create transformative biomedical tools.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Postdoctoral Research Fellow - Generative Biology Institute

Conduct independent, high-impact research in a multidisciplinary environment focused on engineering biology, with responsibilities including experimental design, data analysis, publication, and mentoring junior researchers. Work at the intersection of biology, technology, and engineering within a newly established, well-resourced institute pursuing transformative solutions in health, agriculture, and sustainability.

Ellison Institute of Technology Oxford, United Kingdom £40,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global clinical trials, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The Clinical Trial Supply Manager acts as the key liaison between supply chain and clinical teams, overseeing demand planning, depot management, and compliance across phases I–IV studies. The position emphasizes risk-adjusted, patient-focused planning and continuous improvement in supply operations.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

Manages end-to-end clinical trial supply chains for GSK's global R&D studies, translating protocols into operational supply strategies, ensuring timely delivery of investigational products, and maintaining compliance across phases I–IV. Acts as the primary liaison between clinical teams and supply operations, overseeing demand planning, distribution, and inventory policies while mitigating risks and driving continuous improvement in supply chain performance.

GSK €48,375 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK’s global clinical trials, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The Clinical Trial Supply Manager acts as the key liaison between supply operations and study teams, overseeing demand planning, depot management, and compliance across phases I–IV trials. The position emphasizes risk-adjusted, patient-focused planning within a regulated GxP environment.

GSK €48,375 – €80,625 pa

On-site Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to support benefit-risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK €119,250 – €198,750 pa

On-site Permanent

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK United Kingdom

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. The position requires deep therapeutic expertise in chronic weight management or endocrinology, leadership of cross-functional teams, and active engagement in trial design, regulatory submissions, and lifecycle strategy. The role operates in a hybrid work model and may include responsibilities across the Obesity portfolio.

Pfizer United States £274,500 – £457,500 pa

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.

Pfizer £274,500 – £457,500 pa

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets at Pfizer, with end-to-end accountability for designing, executing, and interpreting global clinical trials. The individual will serve as the primary clinical leader on cross-functional teams, shaping development plans, supporting regulatory submissions, and engaging with external stakeholders. A strong emphasis is placed on strategic innovation, team leadership, and therapeutic expertise in obesity and endocrinology.

Pfizer

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