Summary
Join Precision for Medicine as an experienced CRA or Senior CRA to monitor clinical studies at investigative sites, ensure study progress, and interact directly with clients. You will have previous monitoring experience for Oncology clinical studies in South Korea.
Requirements
- Life science degree and / or equivalent experience
- CRA experience within the CRO or pharmaceutical industry (and working in Oncology)
- Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
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 (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)
- Handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope
Preferred Qualifications
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
- Two+ years of oncology experience
- Study start up activities experience would be an advantage
Benefits
Reasonable travel and work/life balance