Precision for Medicine is looking to hire Clinical Research Associates II/Senior Clinical Research Associates in Belgium to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients by integrating clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.
Requirements
- CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
- Oncology experience is essential.
- Two+ years of oncology experience
- Study start up activities experience
- Experience with Phase I studies
- For Senior CRAs, understanding of financial management
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 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.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
