Snabbfakta

    • Paris

Ansök senast: 2024-06-23

Clinical Research Director

Publicerad 2024-04-24

Clinical Research Director - Paris, France - Permanent

Proclinical is seeking a dedicated and experienced Clinical Research Director (CRD) to manage the clinical activities of a range of products. This is a permanent position located in Paris, France.

Primary Responsibilities:

The ideal candidate will have a strong background in designing and monitoring clinical trials, particularly in the field of cardiometabolic diseases. This role requires a high level of autonomy, strong analytical skills, and a deep understanding of good clinical practices, data handling, and ethical standards. The CRD will also need to demonstrate leadership skills, overseeing a cross-functional team and maintaining strong communication with global clinical sites and external stakeholders.

Skills & Requirements:

  • MD degree is required. Board certification/specialization in cardiology is preferred.
  • Minimum of five years of drug development experience in a pharmaceutical company.
  • Experience in cardiovascular/metabolism clinical research is preferred.
  • Proficient written and oral communication skills in English.
  • Strong interpersonal, communication skills.
  • Excellent problem-solving, conflict-resolution and decision-making skills.
  • The Clinical Research Director will:

  • Lead the cross-functional team to successfully implement clinical trials.
  • Provide medical input to support all activities related to clinical studies.
  • Establish strong relations with clinical trial sites and external stakeholders.
  • Draft study protocols in cooperation with consultants and contractors.
  • Liaise with CROs for the selection and monitoring of clinical sites, data management, and safety reporting.
  • Support the drafting of key clinical documents such as meeting requests, briefing packages for Regulatory Authorities, and Clinical Trial Authorization dossier.
  • Provide clinical input to all study-related documents.
  • Assist with the development of presentations at site initiation visits and video-teleconferences with Investigators.
  • Review Key Results Memos, Clinical Study Reports as well as scientific publications and communications on the project.
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