Related skills
clinical operations oncology veeva ctms fda📋 Description
- Guide and oversee international clinical trials, delivering quality data on time and budget.
- Develop and execute operational plans for oncology trial management.
- Collaborate with cross-functional teams to ensure operational excellence and timely data.
- Manage trial start-up activities, coordinating site selection, feasibility, and docs.
- Deliver site initiation, training, and monitoring per protocols and ICH-GCP.
- Build relationships with investigators and staff to facilitate patient recruitment and retention.
🎯 Requirements
- Bachelor's or advanced degree in a relevant scientific discipline.
- Minimum of 3 years of experience in Clinical Operations; oncology trial management preferred.
- In-depth knowledge of clinical trial regulations, including ICH-GCP and FDA requirements, specific to oncology research.
- Demonstrated experience in managing and executing clinical trials from start-up to closeout.
- Proficiency in using Veeva CTMS.
- Understanding of oncology therapeutic areas and related terminology.
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