Offer summary
Qualifications:
Scientific degree (MD, PhD preferred), 10+ years in clinical research experience, Knowledge of clinical trials processes, Understanding of ICH-GCP regulations, Fluent in spoken and written English.Key responsabilities:
- Establish communication with study sites and stakeholders
- Support study teams with trial operations
- Enhance engagement with long-term site relationships
- Develop strategic site engagement strategies
- Attend meetings and support feasibility activities