Clinical Research Associate I/ Clinical Research Associate II
Related skills
travel clinical trials site monitoring oncology cro📋 Description
- Monitor progress of clinical studies at investigative sites.
- Ensure studies are conducted per protocol and ICH-GCP.
- Coordinate site setup, regulatory submissions, and visits.
- Travel domestically and internationally as required.
- Communicate with investigators and project teams.
- Mitigate study risks and ensure quality outcomes.
🎯 Requirements
- Life science degree or equivalent experience.
- 2+ years as CRA in CRO or pharma/biotech.
- Experience managing biopharma studies.
- Domestic travel up to 50-60% (intl travel possible).
- Excellent communication and organizational skills; team player.
- English plus local language where based.
- Oncology monitoring and study start-up experience preferred.
🎁 Benefits
- Remote-based position with site travel.
- Supportive management and growth opportunities.
- Flexible, work-life balanced culture.
- Influence and impact in a smaller CRO.
- English-language application.
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