Clinical Trial Manager H/F - 95

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work : our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.About the Job

Join Excelya, whereAudacity, Care, and Energydefine who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth GO hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities
- Leading feasibility assessments and organizing cross-functional discussions with experts.
- Coordinating preparation, initiation, and follow-up of clinical studies to ensure on-time delivery.
- Overseeing CTIS submissions and ensuring compliance with regulatory and internal requirements.
- Supervising and developing study documents at country level, aligned with core global documents.
- Driving study performance through dashboards, progress meetings, and proactive communication with vendors and sites.
- Monitoring patient recruitment and implementing engagement initiatives for both sites and participants.
- Managing risks, defining mitigation strategies, and ensuring financial resources are well tracked.
- Maintaining strong and lasting relationships with investigational sites, including visits.
- Ensuring database lock and study closure are achieved according to timelines.