Assist in the organization, implementation and completion of clinical research studies for the Cystic Fibrosis Therapeutics Development Network. Assist the clinical Study Team in the implementation and management of clinical studies. Perform site initiation, monitoring and closeout visits at clinical sites. Perform in-house and on-site research data monitoring. Perform collection and review of essential documents and other Study-related documents. Maintain Trial Master File. Assist in review and editing of Study documents. Conduct research projects in compliance with federal regulations, institutional/ departmental guidelines, and standards of Good clinical Practice (GCP).
- Bachelor’s Degree in a biological science, health-related field, or equivalent job experience.
- At least one (1) year of related experience in life sciences.