Related skills
gcp microsoft office google suite clinical trials etmf📋 Description
- Coordinate trial start-up activities, budgets, contracts, and essential docs
- Track study documentation and activities for trial conduct
- Resolve laboratory queries
- Track start-up timelines and identify improvement opportunities
- Monitor site activation, patient enrollment, and monitoring visits
- Maintain centralized repository for essential study documents (Veeva Vault)
🎯 Requirements
- Bachelor's degree in life science field
- 2+ years in clinical trials as CTC or CTA
- Knowledge of regulatory requirements and GCP
- Multi-task, adapt priorities, and proactively manage risks
- Proficient in Microsoft Office or Google Suite
- High proficiency in Veeva Vault CTMS and eTMF
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