Precision for Medicine is looking to fill a Clinical Research Associate (CRA) position to 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.
Requirements
- Oncology experience is essential
- CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
- Study start up activities experience
- Understanding of financial management (for Senior CRAs)
- Knowledge of ICH-GCP and all applicable regulations and standards
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
- Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations
Other
- 4-year college degree or equivalent experience
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline (preferred)
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Calm, thoughtful, and responsive when things don’t go as planned
- Well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game
