Latest Pharmaceuticals Jobs

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and submission dossiers for global regulatory agencies. The Principal Medical Writer will lead complex writing projects, collaborate with cross-functional teams, and translate clinical and statistical data into clear, compliant narratives. The position emphasizes leadership in document strategy, regulatory interpretation, and the use of automation tools within a hybrid work environment.

GSK Stevenage, United Kingdom CA$118,000 – CA$168,000 pa

Hybrid Permanent

Clinical Operations Specialist (Finance)

The role involves managing financial aspects of clinical trials in the UK, including budget tracking, forecasting, and ensuring timely payments to investigator sites and vendors in compliance with regulations. The specialist supports the local delivery lead, coordinates with global and local teams, and leverages AI and digital tools to improve clinical trial efficiency. Administrative duties include meeting coordination, communication management, and maintaining compliance with SOPs and audit requirements.

GSK United Kingdom

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems used in NHS laboratories and clinical chemistry environments. The engineer will visit customer sites to perform maintenance, troubleshoot issues, and deliver technical solutions while working closely with laboratory staff. The position requires a technically skilled individual with experience in high-value capital equipment and offers extensive product training.

TRS Consulting Salisbury, Wiltshire, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves installing, maintaining, and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will provide on-site technical support, troubleshoot complex equipment issues, and ensure minimal downtime for critical healthcare systems. The position requires strong electronics expertise and customer-facing skills, with full product training provided.

TRS Consulting Chippenham, Wiltshire, United Kingdom £52,000 pa

On-site Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert guidance on Good Clinical Practice (GCP) compliance within clinical trial teams, translating complex regulatory requirements into actionable insights. The individual will lead issue resolution, inspection readiness, and root cause analysis across global clinical programs. Collaboration with cross-functional stakeholders and a focus on risk-based decision-making are central to ensuring high standards of quality and data integrity.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Audit Lead

Lead and develop GMP/GDP audit strategy for a key technology area such as sterile biologics or medical devices, ensuring compliance with global regulations and emerging trends. Conduct complex audits across Pfizer facilities, contract manufacturers, and suppliers, while coaching auditors and driving continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.

Pfizer London, SW7 2AP, United Kingdom £162,900 – £271,500 pa

Remote 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-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

Audit Lead

This role leads GMP/GDP audit strategy and execution for key technology areas such as sterile biologics, medical devices, or small molecule manufacturing within Pfizer’s global supply network. The Audit Lead conducts complex audits at internal sites and external vendors, ensures compliance with global regulations, and drives continuous improvement in quality systems. They provide expert guidance, coach auditors, and collaborate across functions to address risks and support inspection readiness.

Pfizer US$162,900 – US$271,500 pa

Remote 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-related therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £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, 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

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

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