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.)

4-year college degree or equivalent experience
2 (two) years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
Site management or equivalent experience in clinical research
Oncology monitoring experience
Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
Fluency in English and for non-English speaking countries the local language of country where position based
Candidates must reside in Madrid or Barcelona

Clinical Research Associate II

Key skills