Precision for Medicine is looking to hire an experienced CRA II or Senior CRA in France to help the life sciences industry improve the speed, cost, and success rate of bringing life-changing therapies to patients, specifically in Oncology and Rare Disease.
Requirements
- CRA experience within the CRO or pharmaceutical industry (and working in Oncology).
- We require a minimum of 1 year experience as a CRA in Oncology, and can offer CRA II and Senior CRA titles depending on experience level.
- Two+ years of oncology experience
- Study start up activities experience would be an advantage
- For Senior CRAs, understanding of financial management and mentoring experience would be desirable
Responsibilities
- You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
- Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.
- You will also have the opportunity to train and mentor junior staff members.
- You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Other
- You will have previous monitoring experience for Oncology clinical Studies in France and you will be located in Paris or Paris area.
- This is a remote based position with travel to sites for monitoring visits.
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
