Monitor studies at investigative sites per protocol and ICH-GCP
Ensure studies are conducted, recorded, and reported per SOPs
Coordinate study setup: identify investigators, regulatory submissions, pre-study visits
Travel up to 60% on average; international travel as needed
Position can be fully home-based (remote)

🎯 Requirements

University degree life science/pharmacy or related health field
At least 6 months CRA experience in CRO or pharma/biotech
Oncology monitoring experience
Excellent communication and organizational skills; team player
Client-focused approach
Experience with computerized information systems, spreadsheets, word processing, and email
Ability to travel overnight; up to 60% travel
Fluency in English and Turkish
Start-up activities experience (preferred)

🎁 Benefits

Remote/home-based opportunity
Collaborative, supportive team
Focus on work-life balance
Opportunity to grow into protocol expertise

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