Director, Global Clinical Trial Management

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.

The Director, Global Clinical Trial Management is a key member of the Clinical Operations team dedicated to achieving and exceeding business objectives through efficient execution, high quality and timely deliverables of all associated aspects of the clinical trial, in compliance with the clinical protocol, Good Clinical Practice guidelines, standard operating procedures and applicable regulatory requirements.

Summary of Job Responsibilities:

Leadership and Management

• Member of the Clinical Operations Leadership Team

• Lead a global team of internal/external Clinical Trial Managers (CTMs) responsible for the conduct of global, clinical trials across development phases and the Galderma pipeline.

• Provide operational leadership to the clinical trial team, ensuring trials are conducted efficiently and meet regulatory requirements.

• Plan, lead, allocate resources and organise the activities within the group in liaison with the other functional leaders to ensure achievement of set R&D objectives.

• Supervise relationships with CROs and other external vendors contracted by Galderma to perform clinical trial activities.

• Prepare and present regular updates and reports to senior management, stakeholders, and regulatory bodies on the status of a clinical trial.

• Lead the development and improvement of SOPs and working instructions related to Clinical Trial Management.

• Develop training standards for Clinical Trial Managers across all indications and locations.

• Contribute to the building of high performing teams across all Galderma R&D locations.

Clinical Trial Team Management

• Oversee the planning, execution, and reporting of all phases of global clinical trials in compliance with the clinical protocol, Good Clinical Practice, standard operating procedures and applicable regulatory requirements.

• Manage clinical trial progress and ensure completeness of documentation and data collection in adherence with the project timelines.

• Accountable for development and management of line budget and oversight of clinical study budgets; verify clinical activities and approve invoices according to the defined budget.

• Collaborate with the Clinical Trial Excellence team to identify, select, and manage relationships with clinical sites, investigators and external vendors/partners.  Drive sites and vendors to meet aggressive timelines, on budget, and hold them to account if they fall behind.

• Collaborate with the Clinical Supplies Unit to oversee the clinical supply forecast and re-supply.

• Foster a culture of inspection readiness within the organization, ensuring the team aims to always maintain a state of readiness.

• Proactively identify potential risks and develop & implement action plans to avoid or mitigate program risks and make appropriate trade-offs of balancing risks with study deliverables and costs.

• Ensure design, execution and report of clinical studies and clinical documentation to regulatory submissions according to