Latest Business Insights Manager Jobs

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and improving processes.

GSK United States

Hybrid Permanent

Field Service Engineer, Laboratory Robotic Systems

Field Service Engineer, Laboratory Robotic SystemsBasic Salary £50,000 to £55,000Bonus 10%Company Car - Electric (Tesla) and Hybrid Options AvailablePensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Laboratory Robotic SystemsThis market leader seeks to recruit a technically motivated and customer focused...

TRS Consulting Harlow, United Kingdom

Field Service Engineer, Laboratory Robotic Systems

Field Service Engineer, Laboratory Robotic SystemsBasic Salary £50,000 to £55,000Bonus 10%Company Car - Electric (Tesla) and Hybrid Options AvailablePensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Laboratory Robotic SystemsThis market leader seeks to recruit a technically motivated and customer focused...

TRS Consulting Braintree, United Kingdom

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 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

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

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, collaborating with internal and external stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key experts in the field.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.

GSK

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharm, vaccines, and pharmaceutical facilities. Responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports. The role requires strong communication skills and subject matter expertise in sterile manufacturing.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.

GSK

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. You will evaluate compliance with GMP, regulatory requirements, and quality systems, and provide sterile manufacturing expertise. The role requires strong communication and stakeholder engagement skills.

GSK

Hybrid Permanent