Clinical Research Associate II
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Job Description
Clinical Research Associate monitoring oncology trials for Precision for Medicine, a precision-medicine CRO. Managing investigative sites, regulatory submissions, and protocol-compliant study execution.
Responsibilities:
- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- Coordinate activities required to set up and monitor studies
- Identify investigators
- Help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Participate in investigator meetings, site visits, and project team updates
- Identify potential study risks and propose mitigation solutions
- Manage conflict using resolution strategies
- Provide input and ideas to support positive company change
Requirements:
- 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, up to approximately 50–60% travel commitment
- Fluency in English and, for non-English speaking countries, the local language of the country where the position is based
- Candidates must reside in Madrid or Barcelona
- Application must be submitted in English
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline preferred
- Phase I experience preferred
- Experience managing CAR-T/FIH studies preferred
Benefits:
- Extremely high CRA retention rates compared to industry averages
- Lower than average number of protocols
- Reasonable travel commitment
- Improved work/life balance
- Direct line management support
- Opportunities to influence and impact company decisions
- Employee input and ideas valued and nurtured
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