Summary
Join Precision for Medicine, a CRO with high CRA retention rates, offering a unique work environment. This fully remote UK-based CRA II/Senior CRA position prioritizes work-life balance with a lower-than-average protocol workload. You will monitor clinical studies, ensuring compliance with regulations, and contribute to study setup and monitoring. The ideal candidate possesses strong CRA experience, attention to detail, and problem-solving skills. Precision values employee input and offers opportunities for growth and development within a supportive team focused on precision medicine in oncology.
Requirements
- 4-year college degree or equivalent experience
- At least 2 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
- 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
Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
Benefits
- Lower than average number of protocols, setting you up to be a protocol expert
- Reasonable travel and improved work/life balance
- Your voice will be heard and you will have influence and impact
- Support from direct line management
- Fully home based working in the UK
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