Biotechnology Jobs

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 role involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

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 and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

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

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 internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a pharmaceutical manufacturing environment, ensuring compliance with GMP regulations. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer United States

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders. The position also involves mentoring others and contributing to the overall clinical strategy.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.

Pfizer

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.

Pfizer

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.

Pfizer

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to studies. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.

Pfizer

On-site Permanent

Bioinformatician - CRISPR - Cambridge

This role involves working on CRISPR-related projects, developing and maintaining data pipelines, and supporting lab scientists using Python or R. The position requires a minimum of 3 days per week on-site in central Cambridge, with the rest of the time potentially flexible.

Morson Edge Trumpington, Cambridgeshire, CB2 9LS, United Kingdom £400 – £425 pd

Hybrid Contract Flexible

Biomedical Field Service Engineer

This role involves daily repair, preventative maintenance, and asset management of medical devices across multiple hospital locations. Key responsibilities include performing scheduled maintenance, completing repairs, supporting the site manager, and maintaining safe working practices and service documentation. The role requires travel to various sites and maintaining strong customer relationships.

Focus Resourcing Berkshire, United Kingdom

On-site Permanent