Clinical Research Associate II
Remote
Job Summary
Monitor and own the progress of clinical studies at investigative sites, ensuring they are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations. Coordinate all necessary activities to set up and monitor studies, including identifying investigators, preparing regulatory submissions, and conducting pre-study and initiation visits. Identify potential study risks and propose mitigation solutions while maintaining an impeccable eye for detail in quality and outcomes. This role supports Precision for Medicine's mission to revolutionize cancer treatment through precision medicine and biomarker-driven clinical trials. Candidates must reside in Madrid or Barcelona and are fluent in English and the local language.
Required Qualifications
- 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
- Please, apply in English only
Desired Qualifications
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
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