Monitor and own progress of clinical studies at sites per protocol and regs.
Coordinate site setup tasks: investigator identification, regulatory prep, pre-study visits.
Ensure studies are conducted, recorded, and reported per ICH-GCP and SOPs.
Support growth through ongoing study oversight and issue resolution.
Travel up to 50-60% for domestic sites as needed.
Role based in Madrid or Barcelona, Spain; remote work option.

🎯 Requirements

4-year college degree or equivalent experience
2+ years as a CRA in CRO or pharma/biotech
Site management or equivalent clinical research experience
Oncology monitoring experience
Fluency in English; local language for country of posting
Candidates must reside in Madrid or Barcelona

🎁 Benefits

Flexible work-life balance in a smaller CRO
Direct line management support and influence on projects

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