Related skills
travel monitoring clinical trials regulatory submissions oncology📋 Description
- Monitor progress of clinical studies at investigative sites per protocol, SOPs, and ICH-GCP.
- Coordinate study setup and monitoring activities (investigators, regulatory submissions, pre-study and initiation visits).
- Ensure studies are conducted, recorded, and reported per protocol and applicable standards.
- Travel domestically up to 50-60% as required.
- Work in a smaller CRO and have influence on projects and growth.
🎯 Requirements
- 4-year college degree or equivalent.
- 2+ years as a CRA in CRO or pharma.
- Site management or equivalent clinical research experience.
- Oncology monitoring experience.
- Domestic travel up to 50-60%.
- English fluency; local language for non-English countries.
- Candidates must reside in Madrid or Barcelona.
- Graduate or postgraduate degree in science/healthcare (preferred).
🎁 Benefits
- Smaller CRO with close management and influence.
- Excellent work-life balance and supportive culture.
- Opportunity to impact projects and have your voice heard.
- Travel opportunities with reasonable schedules.
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