Central - Regional CRA
Dallas Metro Area, Texas
Full-time position available for Clinical Research Associate (CRA) in the Central Region of the US (TX, LA, WI)
Responsible for monitoring activities in compliance with FDA regulations, ICH/GCP guidelines, and SOPs, The CRA will manage the activities of the clinical investigative sites to ensure successful execution of the protocol. The CRA will also ensure that trial data are accurate, complete, and verifiable from source documents.
Bachelor s degree in life sciences or research related field and two years related experience. Must have at least 2+ years clinical research independent monitoring experience with a good understanding of the clinical development process and associated regulations. CCRP preferred. Relevant work experience should include at least 2 years of Monitoring experience.
- CRO experience
- BS or higher
- Experience as Monitor in Oncology
- Experience conducting all visit types (pre-study, Initiation, Monitor Visits, and Close-out visits)
- Early Phase I experience (preferably in oncology trials)
- Travel up to 75% (at least 3 days a week)