Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Senior Clinical Trial Manager

Location: London, UK
Department: Clinical Operations – Clinical Trial Management
Reports to: Associate Director, Global Clinical Trial Management

At Galderma, we’re unique and we embrace difference

At Galderma, we actively embrace diversity, inclusion and individuality. We believe that our people are at the heart of our success, and we are committed to creating an environment where everyone can bring their authentic selves to work, contribute their unique perspectives and grow their careers.

As the world’s largest independent global dermatology company, we are dedicated to advancing dermatology for every skin story. Our ambition is to empower people and transform lives through innovative solutions in Aesthetics, Consumer Care and Prescription Medicine.

We are looking for a Senior Clinical Trial Manager to join our Clinical Operations team in London.

Senior Clinical Trial Manager

The Senior Clinical Trial Manager (CTM) is responsible for planning and managing the overall activities of assigned global clinical trials, ensuring delivery according to timelines, budget, quality standards and applicable regulatory requirements.

The Senior CTM will work closely with cross-functional teams, Clinical Science Experts, Clinical Scientists and external partners to ensure successful execution throughout the clinical development lifecycle. Depending on the scope of the trial, the role may also provide leadership and oversight to other Clinical Trial Managers.

Key Responsibilities

Clinical Trial Management

• Lead and manage cross-functional Clinical Trial Teams to ensure all trial deliverables are completed according to timelines, budget, quality standards and operational best practices.
• Partner with Clinical Science Experts and Clinical Scientists on clinical trial design and execution.
• Establish study milestones, budgets and timelines in collaboration with the Clinical Trial Team and outsourcing partners.
• Monitor clinical trial progress and ensure appropriate documentation and data collection throughout the study.
• Proactively identify risks and develop and implement mitigation and action plans.
• Contribute to clinical study reporting and documentation supporting regulatory submissions and ensuring compliance with applicable requirements, international standards and the company quality system.
• Provide oversight to Clinical Research Associates and Clinical Trial Administrators, where applicable.

CRO & External Partner Management

• Collaborate with Procurement to define clinical outsourcing requirements and specifications.
• Participate in the selection of CROs and Functional Service Providers (FSPs).
• Act as the primary trial contact for CROs and FSPs and ensure effective oversight of external partners.

Quality & Process Improvement

• Ensure clinical trials remain inspection-ready throughout their lifecycle.
• Participate in inspection readiness activities and support the preparation and conduct of investigational site and health authority inspections, where applicable.
• Contribute to and initiate clinical trial and departmental process improvement initiatives.

What You’ll Bring

• University degree in Life Sciences, such as Biology, Pharmacology, Nursing, Health Sciences or a related discipline.
• At least 10 years of progressive experience in clinical research/operations, including approximately 5 years in a managerial role or equivalent within Pharma, Biotech and/or CRO environments.
• Broad experience across the clinical trial lifecycle, from protocol development through to study reporting.
• Experience managing clinical trials in major markets, particularly the US and/or China.
• Proven experience supervising and managing CROs and external service providers.
• Strong understanding of the drug development process, with systemic drug and biologics experience preferred.
• Excellent knowledge of ICH/GCP guidelines, with a working knowledge of GMP/GDP.
• Strong knowledge of relevant local regulatory requirements.
• Excellent communication, project management and stakeholder management skills.
• Fluent written and spoken English.

What we offer in return

At Galderma, you will have the opportunity to work in a dynamic, international and purpose-driven environment where you can make a meaningful contribution to the future of dermatology.

We offer an environment that supports professional development, collaboration and continuous learning, with the opportunity to work alongside talented colleagues across the globe.

Next Steps

If you are excited about this opportunity and believe your experience and skills could be a good match, we encourage you to apply.

Our recruitment process is designed to give you the opportunity to learn more about Galderma, the role and the team, while allowing us to get to know you and your experience.

Our people make a difference

At Galderma, we believe that our people are what make the difference. We are committed to building an inclusive workplace where diverse perspectives are valued and everyone has the opportunity to contribute, develop and grow.

We are proud to be an equal opportunity employer and welcome applications from all qualified candidates, regardless of background, identity or individual circumstances.