Senior Clinical Trial Manager
About this role
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our bold 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
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.