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site monitoring regulatory submissions oncology sops ich-gcp📋 Description
- Monitor progress of clinical studies at investigative sites.
- Ensure studies are conducted per protocol and ICH-GCP.
- Coordinate site setup and monitoring activities.
- Remote-based with travel to sites for morning visits.
- Be a protocol expert with strong attention to detail.
- Collaborate with cross-functional teams to support studies.
🎯 Requirements
- Life science degree or equivalent experience.
- At least 1.5 years CRA experience in CRO/pharma; site management.
- Oncology monitoring experience.
- Domestic travel incl. overnight stays; some international travel.
- English and local language fluency.
- Excellent communication and organizational skills; client-focused.
- Preferred: Study start-up activities experience.
🎁 Benefits
- Remote role with site travel as needed.
- Exposure to oncology and rare disease trials.
- Strong team culture and growth opportunities.
- Impactful clinical research work.
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