Director, Global Clinical Trial Management

At Galderma we're unique and we embrace difference.

Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising 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.

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 plan and in compliance with applicable regulatory requirements, international standards and the company quality system throughout the development life cycle

• May temporarily serve as a CTM providing support as needed or independently managing clinical protocols

Minimum Requirements:

• University degree required in Life Sciences such as biology, pharmacology, nursing, or health sciences

• Progressive experience in clinical research/operations (≥15 years), including 5 years in a managerial role or equivalent with Pharma/Biotech and/or CRO experience

• Experience from all parts of the clinical trial process, from protocol development to the compilation of study reports

• Experience as manager of clinical trials in major market(s) such as US, China

• Experience in supervising CROs.

• Excellent understanding of the drug development process, systemic drug and biologics experience preferred

• Excellent knowledge of international ICH/GCP guidelines, basic knowledge of GMP/GDP

• Excellent knowledge of relevant local regulations

• Fluent in English (written and oral)

What we offer in return:

You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base. You will also have access to a range of company benefits, including a competitive wage with shift differential, annual bonus opportunities and career advancement and cross-training.

Next Steps:

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.

• The next step is a virtual conversation with the hiring manager

• The final step is a panel conversation with the extended team

• Our people make a difference

• At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Employer's Rights:

This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. You will be evaluated in part based on your performance of the tasks listed in this job description. The employer has the right to revise this job description at any time. This job description is not an employment contract, and either you or the employer may terminate employment at any time, for any reason. In addition, reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.