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site monitoring regulatory submissions oncology ich-gcp cra certification📋 Description
- Monitor clinical studies at sites per protocol, SOPs, and ICH-GCP.
- Coordinate setup and monitoring: investigators, regulatory submissions, visits.
- Remote-based role (Italy) with travel to sites for visits.
- Travel availability up to 50-60% domestically.
🎯 Requirements
- University degree in life sciences/pharmacy or healthcare.
- At least 6 months CRA experience in CRO or pharma.
- Oncology experience.
- CRA Certification holder.
- Availability for travel up to 50-60%.
- Fluency in English and Italian.
🎁 Benefits
- Remote-based position in Italy with site travel.
- Good work-life balance and supportive management.
- Lower protocol load enables protocol expertise.
- Opportunity to influence outcomes in a smaller CRO.
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