Education
Bachelors degree in clinical research, science or other healthcare related field preferred.
Master’s degree in clinical research, science or other healthcare related field preferred
Certification/Licensure
CCRP or CCRC certification preferred
Experience
Three or more years of clinical research experience required (site management, study management, IRBs, and federal regulations regarding clinical research compliance)
Other
Knowledge of, or ability to learn, electronic health systems and databases used in research environments
•Knowledge of, or ability to learn, participant and sample collection for large scale initiatives
•Experience in the use of Microsoft Office, including Word, Excel, and Power Point
•Ability to function independently as well as part of an interdisciplinary team and interact with a variety of administrative and professional personnel
•Strong follow-through skills and ability to proactively identify and solve problems; demonstrating initiative is imperative
•Ability to effectively communicate using oral and written skills
•Ability to be detail oriented and the ability to ensure resolution and compliance
•Ability to work independently using initiative and good judgment
•Working knowledge of the applicable regulations related to product or agent being studied, the specific protocol, the informed consent process, and the sponsors’ policies and procedures
•Working knowledge of regulation and guidance(s) related to clinical research
Current full vaccination status required