Senior Clinical Research Associate I at IQVIA, responsible for site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements.
- Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements.
- Ensure investigational sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality.
- Build and maintain effective relationships with investigators and site personnel, providing ongoing guidance, training, and support throughout the study lifecycle.
- Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics.
- Collaborate with sites to implement and optimize patient recruitment and retention strategies to support study timelines.
- University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.
- Nice to have: sponsor-dedicated or cFSP environment
- Nice to have: patient recruitment and study start-up activities
Clinical Research Coordinator III - School of Medicine, DermatologyNewEmory University · Atlanta, US