Clinical Trial Manager – Contract

This is a fully remote position, open to applicants in France.

📋 Description

• Oversee the operations for studies sponsored by Resilience as well as those initiated by investigators across multiple therapeutic areas.

• Manage day-to-day operations and logistics related to the studies.

• Assist in the planning and follow-up for site selection, initiation, monitoring, and close-out visits.

• Monitor site progress, study metrics, and data integrity.

• Raise issues that need addressing during study meetings and governance committees.

• Follow up on site agreements, amendments, and budget annexes.

• Aid in tracking site budgets and follow up on payments with the Legal and Finance departments.

• Keep regulatory documentation and the electronic Trial Master File (eTMF) updated.

• Ensure audit readiness and compliance with Good Clinical Practice (GCP), applicable International Council for Harmonisation (ICH) guidelines, the French Jardé Law, and GDPR.

• Collaborate with Clinical Scientists, Biostatistics, Product, Legal, and Finance teams.

• Enhance clinical operations trackers, standard operating procedures, and templates.

• Report directly to the Clinical Operations Lead.

⛳️ Requirements

• Bachelor's degree in life sciences, pharmacy, clinical research, or biomedical engineering.

• Minimum of two years' experience in clinical research, such as a Clinical Research Associate (CRA), site manager, or junior project manager.

• Proven experience in operational follow-up of clinical sites or studies.

• Proficient in organizing clinical study activities and tracking priorities, deadlines, and actions among stakeholders.

• Familiarity with GCP, relevant ICH guidelines, the French Jardé Law, and GDPR.

• Competence in maintaining organized study documentation and utilizing study indicators to assess progress.

• Experience or capability in contributing to regulatory submission follow-up, site contracting, and budget tracking.

• Professional proficiency in both French and English, in written and spoken forms.

• Organized, detail-oriented, and able to work independently.

• Skillful in prioritizing tasks effectively and communicating across various functions.

• Approach characterized by collaboration, adaptability, curiosity, and resourcefulness.

🏝️ Benefits

• Fully remote position within France.

• Regular travel associated with the role.

• Opportunity to engage in studies that merge clinical research, digital tools, and patient-centered monitoring.

• Chance to enhance regulatory and contractual coordination skills.

• Work across a range of therapeutic areas with complementary disciplines.

• Opportunity to refine methods and tools in clinical operations.

• Team celebrations and a culture focused on practical, collaborative problem-solving.