Duties and Responsibilities
Assists Primary Coordinator with
Ensure the filing and maintenance of all study documents
Other duties as assigned
2-3 years clinical research experience
Computer literacy, proficiency in MS Office
Able to read, analyze, and interpret information from charts, technical procedures, or governmental regulations.
Able to effectively present information and respond to questions from physicians, staff and patients.
Knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research required.
Ability to adapt to changes throughout the day. work independently and function effectively in a team setting
Needs to demonstrate consistent professional conduct and meticulous attention to detail
Travel to investigator sites and meetings when necessary
- We are a growing investigtor site. Qualified Asst. CRCs can move up to CRC position quicikly