Precision for Medicine is looking to solve the problem of improving the speed, cost, and success rate of bringing life-changing therapies to patients in the life sciences industry, particularly in Oncology and Rare Disease.
Requirements
- Life science degree and/or equivalent experience
- 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
- Experience managing oncology studies
- Site management or equivalent experience in clinical research
- Study start up activities experience (preferred)
- Fluency in English, Dutch and French
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
- Identify potential study risks and propose solutions on how to mitigate them
- Take responsibility in the quality and outcomes of your work
- Conduct pre-study and initiation visits
- Help prepare regulatory submissions
Other
- Excellent communication and organizational skills are essential
- A team player
- Evidence of a client focused approach
- Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
- Life science degree
