Related skills
edc regulatory submissions oncology site management ich-gcp📋 Description
- Monitor studies at sites to ensure protocol and ICH-GCP compliance.
- Coordinate site setup and monitoring: investigators, regulatory submissions, visits.
- Manage trials and support Project Managers on larger studies.
- Train and mentor junior staff; interact with clients; support proposals.
- Travel up to 60% as required.
- Remote/home-based role with flexible work arrangement.
🎯 Requirements
- University degree in life sciences/pharmacy or licensed healthcare professional.
- 3.5+ years as CRA in CRO/pharma with site management experience.
- Oncology monitoring experience.
- Excellent communication and organizational skills; team player.
- Travel up to 60% and international travel as needed.
- Fluency in English and Turkish.
🎁 Benefits
- Supportive team and strong retention.
- Growth and mentoring opportunities.
- Impactful work in oncology and precision medicine.
- Engaging, collaborative culture.
- Voice heard and direct management support.
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