Excelya

Clinical Research Director

🇫🇷 Boulogne-Billancourt, Франція Гібридно Охорона здоров'я та наука Повна зайнятість Керівництво Опубліковано Тра 27, 2026
Формат роботи Гібридно
Тип зайнятості Повна зайнятість
Рівень досвіду Керівництво
Мова English
Опубліковано 27 травня 2026 р.
Остання перевірка 27 травня 2026 р.
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Clinical Research Director at Excelya: Boulogne-Billancourt, Франція; Гібридно; Повна зайнятість; Керівництво; Охорона здоров'я та наука. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Boulogne-Billancourt, Франція, Гібридно
  • Role classification: Охорона здоров'я та наука, Повна зайнятість, Керівництво
  • Source freshness: checked by JobGrid on 2026-05-27.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. As the Clinical Research Director for Inflammation and Immunology (I&I), you will lead critical clinical programs and play a pivotal role in advancing innovative therapies for patients.

This remote role empowers you to influence clinical strategy significantly, ensuring that we not only meet regulatory standards but also create optimal study designs that translate into successful patient outcomes.

Main Responsibilities:

Lead the clinical development of projects in the Inflammation and Immunology therapeutic area from inception through to the successful execution of clinical trials

Ensure compliance with regulatory requirements, ICH-GCP principles, and internal procedures throughout the trial lifecycle

Develop and approve key clinical documents including protocols, informed consent forms, and study amendments

Work closely with cross-functional teams to define clinical strategy, operational processes, and delivery timelines

Serve as the primary medical and scientific contact for Health Authorities, Ethics Committees, investigators, and key stakeholders

Oversee and guide the design, governance, and conduct of clinical committees, ensuring adherence to governance standards

Conduct medical assessments of data, engage in data review processes, and provide insights on protocol deviations and safety monitoring

Participate in the development and review of clinical study reports and publications

Lead the training and mentorship of clinical teams and CRO partners to ensure effective study execution

Represent Excelya in external forums, conferences, and meetings to communicate scientific and strategic objectives