Research Administrator for Clinical Trials
1 semana atrás
**Job Summary:**
We are seeking a highly organized and detail-oriented Research Administrator to join our team in Paris, France.
About ICON:
ICON plc is a world-leading healthcare intelligence and clinical research organization. We accelerate the development of drugs and devices that save lives and improve quality of life.
Your Role:
As a Research Administrator, you will assist in the coordination and administration of clinical studies from start-up to execution and close-out. You will work closely with the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables.
Key Responsibilities:
- Collect and review documents for the application process
- Ensure timely submission of proper application/documents to EC/IRB and Regulatory Authorities
- Interface with Investigators, external service providers, and CRAs during document collection
- Operational responsibility for eTMF and ISF setup and maintenance
- Contribute to the production and maintenance of study documents
Requirements:
- High school/Secondary school qualifications supporting skills and capabilities
- Previous administrative experience in medical/life science field
- Proven organizational and administrative skills
- Computer proficiency
- Good knowledge of spoken and written English
What ICON Offers:
- Competitive salary: €45,000 - €60,000 per annum
- Variety of annual leave entitlements
- Range of health insurance offerings
- Global Employee Assistance Programme
- Flexible country-specific optional benefits
Join Our Team:
We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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