Latest IT Recruitment Jobs

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver on program objectives and commitments.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.

Moderna Tameside, SK15 3JG, United Kingdom

On-site Permanent

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Scientist I, Molecular and Cell Biology

This role involves conducting cutting-edge research in molecular and cell biology, focusing on cell health and rejuvenation. Responsibilities include designing and executing experiments, developing new assays, and collaborating with multidisciplinary teams to advance translational projects and validate therapeutic targets.

Altos Labs Cambridge, United Kingdom £51,500 – £67,700 pa

On-site Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Scientist / Senior Scientist, Computational Biology

This role involves designing and executing computational strategies to analyze large-scale omics data, developing robust bioinformatic pipelines, and collaborating with cross-functional teams to advance aging and rejuvenation research. The position requires a PhD in Life Science or Computational Biology, with a focus on high-throughput data analysis and strong programming skills.

Altos Labs Cambridge, 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. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

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

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves creating clinical development plans, providing expert input on trial design and execution, and engaging with external stakeholders to drive strategic insights and support regulatory submissions.

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, executing, and interpreting clinical studies, 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 US$214,900 – US$358,100 pa

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 ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

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 (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