Clinical Research Associate

☞ Randstad Switzerland

View: 202

Update day: 24-04-2024

Location: Plan-les-Ouates Genève GE

Category: R & D IT - Software

Industry: Staffing Recruiting Biotechnology Research Pharmaceutical Manufacturing

Position: Entry level

Job type: Full-time

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Job content

We are looking for our client, a growing and dynamic medical device company based in Geneva, a:

Clinical Research Associate

Your Responsibilities
  • You are responsible for the supporting of the clinical studies and for clinical study management especially:
  • You prepare the study sites for site initiation.
  • You develop the monitoring plan and related documents.
  • You support the regulatory submission process.
  • You conduct site initiation, monitoring and site closure, ensuring the documentation is maintained.
  • You support the development of a patient enrolment plan and investigate patient enrolment delays.
  • You oversee safety reporting, track study reported adverse events, write safety narratives, coordinate safety reviews.
  • You support Clinical Study Coordinator as needed (contracts, TMF, invoices, etc).
Your Profile
  • You are a registered Nurse or have an equivalent medical background or bachelor’s degree in a healthcare or other life sciences discipline.
  • You have experience in clinical study monitoring on-site.
  • You have a knowledge of Good Clinical Practice relating to medical device studies.
  • You have excellent communication and collaboration skills.
  • You have a high sense of responsibility and reliability.
  • You are competent in English and French, and additional skills in Spanish.
  • You are flexible to travel intermittently up to 30%.
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Deadline: 08-06-2024

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