Precision for Medicine is looking to solve the problem of improving 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
- oncology experience
- fluency in Dutch and English
- experience with Phase I studies
- study start up activities experience
- understanding of financial management (for Senior CRAs)
- fluency in French (preferred)
Responsibilities
- monitor and own the progress of clinical studies at investigative sites
- ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- coordinate all necessary activities required to set up and monitor a study
- handle appropriately sized clinical trials
- support Project Managers with trials that are larger in scope
- train and mentor junior staff members
- interact directly with clients, initiate payments, and participate in proposal activities
Other
- 4-year college degree or equivalent experience
- availability for domestic travel including overnight stays (up to 50-60% travel commitment)
- graduate or postgraduate degree with a concentration in a scientific or healthcare discipline (preferred)
- 2+ years of oncology experience (preferred)
- ability to work in a remote setting
