Summary
Join Precision for Medicine, a CRO with high CRA retention rates, offering a unique work environment. As a CRA II, you will be fully home-based in the UK, enjoying a lower-than-average protocol workload and reasonable travel. Your work-life balance will be prioritized, and your voice will be heard within the company. You will monitor clinical studies, ensuring compliance with protocols and regulations. The role requires a 4-year college degree or equivalent experience and at least one year of CRA experience in the CRO or pharmaceutical industry. Oncology experience is desirable but not essential.
Requirements
- 4-year college degree or equivalent experience
- At least 1 years CRA experience within the CRO or pharmaceutical industry
- 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)
- Fluency in English
Responsibilities
- 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
- 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.)
Preferred Qualifications
- Oncology experience
- Early phase experience