Clinical Trial Manager

Excelya

  • Boulogne-Billancourt, Hauts-de-Seine
  • CDI
  • Temps-plein
  • Il y a 7 jours
  • Postuler facilement
About the JobJoin Excelya, where Audacity, Care, and Energy define 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.
RequirementsAbout YouAt Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values.
  • Experience: Proven experience in managing international clinical operations (avoid requiring minimum years—talent matters most to us!)
  • Skills: Experience in clinical research, ideally as a Clinical Project Manager or equivalent, Solid knowledge of clinical trial regulations, CTIS submissions, and site management, Excellent communication and relationship-building skills with investigational sites and cross-functional teams.
  • Education: Degree in Life Sciences or related field
  • Languages: Proficiency in both English and French (written and spoken).
BenefitsWhy Join Us?At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.Here's what makes us uniqueWe are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission

Excelya