Overview
As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to bring life-changing treatments to patients faster.
This is your opportunity to be part of an exclusive, high-impact program where you can lead by example and shape the standard for clinical excellence.
- Location: Paris-based role – 2 days per week at ICON’s office in Puteaux or onsite visits, and 3 days home-based
- Profile: We welcome experienced CRA professionals from both CRO and public sector backgrounds
- Requirement: Minimum 2 years of independent monitoring experience is essential
Responsibilities
Key responsibilities include:
- Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
- Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
- Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
- Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines
Qualifications
You will need:
- A first stable experience as a CRA (min 2-3 years)
- Interested in different Therapeutic Areas
- Excellent organization skills
- Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
- Strong IT skills
- Strong communication with the ability to multitask and work effectively under pressure
- Fluency in French and professional proficiency in English
#LI-KD1