Related skills
clinical trials site monitoring regulatory submissions oncology ich-gcp📋 Description
- Monitor studies at investigative sites per protocol, SOPs and ICH-GCP.
- Coordinate study setup and monitoring; identify investigators; assist submissions.
- Remote-based position with travel to sites for morning visits.
- Oncology and Rare Disease focus with strong CRA retention.
🎯 Requirements
- Life science degree or equivalent
- At least 6 months CRA experience in CRO/pharma or equivalent
- Oncology experience
- Domestic travel 50-60%; some international travel possible
- Excellent communication and organizational skills; team player; client-focused
- English fluency; local language as needed; study start-up experience (preferred)
🎁 Benefits
- Remote work with site visits
- Strong culture with CRA retention and work-life balance
- Opportunity to develop protocol expertise
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