Clinical Research Project Manager - H/F

Description

Primary Responsibilities

Reporting to the project leader and working in close collaboration with the Inserm Clinical Research Division, the successful candidate will be responsible for the following tasks. • Project coordination and governance, including in particular • Communication, reporting, and representation • Scientific, regulatory, and operational oversight

Primary Activities

Project coordination and governance

Supporting the overall coordination of an international clinical research project involving multiple institutional, academic, and clinical partners in Europe and Africa. Contributing to the establishment, monitoring, and facilitation of the project’s governance bodies (steering committee, scientific committee, technical committees). Organizing, preparing, and following up on multi-partner meetings, drafting meeting minutes, and tracking decisions. Serving as a central liaison and facilitator between scientific teams, clinical sites, the Inserm Clinical Research Center, institutional partners, and the European funding body.

Communication, Reporting, and Representation

Coordinating and contributing to the preparation of scientific and financial reports for the EDCTP. Preparing and delivering oral presentations to expert scientific audiences and institutional bodies. Contribution to project promotion Support for the consortium’s internal communication to ensure the smooth flow of information.

Scientific, Regulatory, and Operational Monitoring

Cross-functional monitoring of the scientific and operational progress of work packages, in close collaboration with their leads. Support for the management of regulatory, ethical, and institutional procedures specific to international clinical trials, particularly in LMICs, in collaboration with the Inserm Clinical Research Center and local experts. Monitoring of project deliverables, milestones, and indicators, in accordance with European funding requirements.

Specifics and work environment

Potential variability in work schedules Short-term international assignments over multiple years

Profil recherché

Knowledge

Strong organizational, prioritization, and follow-up skills. Project management skills, including documentation. Fluency in English (spoken and written). Solid background in clinical research and a strong interest in infectious diseases and therapeutic research

Skills

Project coordination Independence, adaptability, and ability to work in a multi-site setting Strong motivation for health research in LMICs, particularly in Africa

Skills

Fluency in written and oral communication before an expert scientific audience. Diplomatic approach and strong interpersonal skills in multicultural environments. Independence Rigor Excellent ability to work in a team Flexibility

Desired Experience

Two years of experience Operational health research Experience in LMICs

Degree Level and Education

Master’s degree (5 years of higher education) with a specialization in health & international relations and clinical research. DIU FIEC, project manager certification, or equivalent experience

Start Date

May 1, 2026