Clinical Project Manager
Randstad
Geneva, Genf, CH
vor 5 Tg.

Key Responsabilities :

  • Responsible for the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries (EU, US, ), in accordance with the applicable legislation and Company Standard Operating Procedures.
  • Responsible for the operational management of clinical studies, ensuring the compliance with timelines, milestones and budget.
  • Act as the main line of communication to relevant stakeholders and provides input to feasibility, study design, budget development and ensures progress reporting (resources, budget and timelines).
  • Lead the monitoring team(s) in the designated country / countries for his / her trials and ensures the team is trained properly.
  • Provide input on study related documents (e.g. ICF, CRF, monitor plan, protocol, studyProcedure Manual etc.), set-up and maintain study files.
  • Profile : - Degree in health care, life sciences or related fields.- Minimum of 3 years of experience in clinical research.

  • Knowledge of clinical trial design and development.- Experience with coordinating a team.- In-depth knowledge of EU and US legislation and Procedures. - Fluent in English.
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