Clinical Research Associate II

Job Description

Monitor and manage the progress of clinical studies at investigative sites, ensuring quality and adherence to protocols. Guarantee clinical studies are conducted, documented, and reported in accordance with established protocols, SOPs, ICH-GCP guidelines, and all relevant regulations and standards. Coordinate activities required to initiate and monitor a study, including investigator identification, regulatory submission preparation, and pre-study and initiation visits.

Qualifications

1. Possess a 4-year college degree or equivalent experience. 2. Have a minimum of two years of experience as a CRA in either a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and demonstrated competencies. 3. Demonstrate site management experience or equivalent in clinical research. 4. Possess oncology monitoring experience. 5. Be available for domestic travel, including overnight stays, which may constitute approximately 50-60% travel commitment. 6. Be fluent in English and, for non-English speaking countries, the local language of the country where the position is based. 7. Reside in Madrid or Barcelona.

Benefits

- Precision’s uniquely integrated offering. - Opportunities for growth and influence.