Clinical Research Associate
View: 235
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
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).
- 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%.
Deadline: 08-06-2024
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