Latest Pharmaceuticals Jobs

Principal Medical Writer

Author and lead the development of high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and CTD submissions. Interpret complex clinical and statistical data to produce accurate, compliant narratives. Collaborate with cross-functional teams and manage complex writing projects across therapeutic areas and global submissions.

GSK CA$118,000 – CA$168,000 pa

Hybrid 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

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings, including on-site troubleshooting and breakdown response. The engineer will work with high-value, complex equipment and provide technical solutions directly to laboratory staff. Full product training is provided, and the role requires a flexible schedule with some weekend work.

TRS Consulting Portsmouth, Hampshire, United Kingdom £52,000 pa

Senior Principal Developer

Develop and maintain R packages and Shiny applications to support clinical trial data analysis and reporting workflows. Collaborate with statisticians and programmers to build reproducible, AI-enhanced tools, with a focus on open-source practices and modernization. Support user experience improvements and drive adoption through training and documentation.

Novartis £57,050 – £105,950 pa

Remote Permanent

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent

Senior Director, Targets and Mechanisms Solutions

Leads the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, overseeing a global team to deliver scalable, science-centric digital solutions that support target identification, translational research, and data integration across therapeutic areas. Drives product management, ecosystem architecture, and the adoption of advanced technologies including AI, predictive analytics, and large-scale omics data systems. Collaborates closely with R&D and digital teams to align technology roadmaps with research priorities and accelerate drug discovery.

Pfizer £230,900 – £384,800 pa

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

Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Director, Clinical Science – Oncology Clinical Development

Lead scientific contributions to oncology clinical studies, focusing on protocol design, data interpretation, and regulatory documentation within a global matrix team. Provide expert input to clinical development plans and collaborate with cross-functional teams to advance cancer therapies. Engage with external experts and support regulatory submissions to drive patient impact.

GSK PLN 472,500 – PLN 787,500 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Leads scientific components of oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with development goals. Focuses on generating robust clinical insights to advance cancer therapies in high unmet need areas.

GSK US$189,750 – US$316,250 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory deliverables within a defined clinical programme. Works closely with cross-functional teams and external experts to ensure scientific rigor and data integrity. Focuses on advancing cancer therapies with high unmet need through robust clinical science and collaboration.

GSK US$189,750 – US$316,250 pa

Hybrid Permanent

Medical Director, Oncology Clinical Development - Hematology

This role involves providing medical leadership in oncology clinical development, with responsibilities spanning study design, medical monitoring, safety oversight, and data interpretation. The Medical Director will integrate physician-level insights into clinical trials, collaborate with cross-functional teams and external experts, and contribute to regulatory submissions and scientific communications. The position emphasizes patient-centered decision-making and real-world impact in cancer treatment innovation.

GSK £222,750 – £371,250 pa

Hybrid Permanent

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the design and execution of real-world evidence (RWE) and health outcomes studies to support GSK's hepatology assets across the product lifecycle. Drive scientific credibility in value-based evidence generation, aligning with regulatory, reimbursement, and payer requirements. Collaborate with cross-functional teams and external experts to translate evidence needs into impactful research strategies.

GSK Canterbury, United Kingdom

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Leads the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology assets. Works cross-functionally to align evidence generation with regulatory, reimbursement, and market access needs, ensuring robust data supports product value and patient access. Engages with internal teams and external experts to translate scientific insights into impactful health outcomes strategies.

GSK United States £185,250 – £339,625 pa

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology assets, ensuring robust data for market access and reimbursement. Collaborate with cross-functional teams and external experts to generate impactful evidence on product value. Drive scientific credibility in study planning, analysis, and dissemination across the product lifecycle.

GSK

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology assets. Collaborate with cross-functional teams to generate robust data for regulatory, reimbursement, and market access decisions. Drive scientific credibility in study design, analysis, and dissemination across the product lifecycle.

GSK