Latest Pharmaceutical Scientist Jobs

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

Director, Clinical Trial and Data Transparency

This role involves leading the strategic and operational aspects of clinical trial transparency and disclosure, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes for compliance.

Pfizer

Remote Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain

On-site Permanent Flexible

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Key responsibilities include driving technology strategy, leading AI and automation initiatives, shaping GTCS-related technology changes, and enabling data-driven decision-making to support strategic and operational insights.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

VP, Strategy & Consulting Lead, International Commercial

ROLE SUMMARYReporting to the SVP, Strategy & Consulting (S&C), this role serves as the strategy lead for Pfizer’s International Commercial Division (ICD) which consists of the commercial functions and corresponding P&L in all ex-U.S. markets. ICD includes key standalone markets...

Pfizer United States

VP, Strategy & Consulting Lead, International Commercial

ROLE SUMMARYReporting to the SVP, Strategy & Consulting (S&C), this role serves as the strategy lead for Pfizer’s International Commercial Division (ICD) which consists of the commercial functions and corresponding P&L in all ex-U.S. markets. ICD includes key standalone markets...

Pfizer

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis, automation, and reporting workflows. The developer will collaborate with statisticians and clinical teams to deliver efficient, reproducible tools, while promoting best practices in data science and software development. A strong focus is placed on responsible AI integration, open-source collaboration, and modernizing clinical reporting through user-centric design and tooling.

Novartis London, United Kingdom £57,050 – £105,950 pa

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on aligning regional regulatory approaches with global objectives and managing Health Authority interactions.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Operations Resource Planner

This role involves partnering with stakeholders to gather and validate submission planning information, ensuring efficient resource allocation for regulatory submissions. You will contribute to process improvements and deliver metrics to support leadership decisions.

Novartis London, United Kingdom

Hybrid Permanent

Risk Surveillance Lead

The Risk Surveillance Lead drives the adoption of RBQM practices in clinical trials, overseeing risk assessment, documentation, and continuous improvement. They work closely with cross-functional teams to ensure quality risk management and compliance with regulatory standards.

Novartis London, United Kingdom

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis and reporting. The developer will collaborate with statisticians and clinical teams to build automated, reproducible tools, while promoting open-source practices and responsible AI integration. Emphasis is placed on modernizing workflows through user-centric design, documentation, and deployment in production environments.

Novartis £57,050 – £105,950 pa

Remote Permanent