Senior Clinical Research Associate
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Job Description
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Ensuring protocol compliance, site oversight, and sponsor collaboration across Spain.
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 applicable regulations and standards
- Coordinate activities required to set up and monitor studies
- Identify investigators and help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Handle appropriately sized clinical trials
- Support larger clinical trials with clinical study teams
- Train and mentor junior staff members
- Interact directly with clients
- Initiate payments
- Participate in proposal activities, including development and client presentations
Requirements:
- 4-year college degree or equivalent experience
- Holder of CRA certificate
- Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
- Extensive experience in IVD (In Vitro Diagnostics), oncology, infectious diseases and gastrointestinal studies
- Proven experience monitoring studies across multiple European countries
- Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment
- International travel may be required for some senior level positions
- Fluency in Spanish and English is required
- Additional language(s) considered an asset
- Study start-up activities experience preferred
- Understanding of financial management preferred for Senior CRAs
Benefits:
- Fully home-based within Spain
- Professional development
- Career growth opportunities
- Empowerment to make an impact
- Meaningful client relationships
- Equal opportunity employment
- Reasonable accommodation during the application process
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