Latest Pharmaceuticals Jobs

Device Technologist - 12 Month Secondment

The Device and Packaging Technologist provides technical support for device assembly and packaging activities, including new product introduction, change control, and continuous improvement. The role involves collaborating with site teams, central technology functions, and external suppliers to ensure compliant and efficient solutions throughout the product lifecycle.

GSK Barnard Castle, United Kingdom

On-site Contract

Vials Filling & Inhalations Operations Manager

This role involves leading vials filling and inhalation device production at a GSK manufacturing site, ensuring safety, quality, and compliance. You will manage day-to-day operations, coach team members, and drive continuous improvement projects.

GSK Barnard Castle, United Kingdom

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer United States

On-site Permanent

Inspection Assembly & Packaging Operations Manager

You will lead inspection, assembly, and packaging operations at a GSK site in the UK, managing day-to-day production, quality, and safety while coaching your team to improve. You will work closely with quality, engineering, and supply chain colleagues to deliver on-time, compliant output and drive continuous improvement projects.

GSK Barnard Castle, United Kingdom

On-site Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK

Hybrid Permanent

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.

GSK United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK United Kingdom

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capabilities.

GSK

Hybrid Permanent