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Galderma

Independent dermatology company delivering skincare therapies

Senior Clinical Trial Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLondon, UKNo salary listedIn-person

About the Job

Requirements

  • A 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 or operations, including approximately 5 years in a managerial role or equivalent within Pharma, Biotech, or CRO environments.
  • Broad experience across the clinical trial lifecycle, from protocol development through 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.
  • A strong understanding of the drug development process.
  • Excellent knowledge of International Council for Harmonisation Good Clinical Practice (ICH/GCP) guidelines and working knowledge of Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
  • Strong knowledge of relevant local regulatory requirements.
  • Excellent communication, project management, and stakeholder management skills.
  • Fluent written and spoken English.

Responsibilities

  • Plan and manage the overall activities of assigned global clinical trials, ensuring delivery according to timelines, budget, quality standards, and applicable regulatory requirements.
  • Lead and manage cross-functional Clinical Trial Teams to ensure 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, ensuring compliance with applicable requirements, international standards, and the company quality system.
  • Provide oversight to Clinical Research Associates and Clinical Trial Administrators, where applicable.
  • Collaborate with Procurement to define clinical outsourcing requirements and specifications.
  • Participate in the selection of Contract Research Organizations (CROs) and Functional Service Providers (FSPs).
  • Act as the primary trial contact for CROs and FSPs and ensure effective oversight of external partners.
  • 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.

Desired Qualifications

  • Systemic drug and biologics experience is preferred.

About the Company

Galderma

Independent dermatology company delivering skincare therapies

Dermatology-focused company that develops and markets prescription and over-the-counter skincare products, plus injectable aesthetics and therapeutic dermatology treatments. Its products use scientific skin research combined with consumer insights to treat conditions, improve appearance, and support everyday skin health. It stands out as an independent dermatology specialist with a deep skin-science heritage and a footprint across prescription, OTC, and aesthetic medicines. Its goal is to be a global leader in science-based solutions for skin conditions, expanding across therapies, aesthetics, and skincare while funding ongoing innovation.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Lausanne, Switzerland
Founded
1981

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