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 – home based + **Profile:** We welcome experienced CRA professionals from both **CRO** and **pharma sector** backgrounds + **Requirement:** Minimum **2 years of independent monitoring experience** is essential 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 You will need: + A first stable experience as a CRA (min 2 years) + Interested in oncology trials + 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