Clinical Research Associate (On Site)
The Clinical Research Associate is responsible for independently monitoring/managing investigative sites to ensure that all clinical trial activities conform to the protocol, GCP-ICH guidelines, local regulations, statutes, and SOPs. This person is also responsible for assisting the CTM and/or Associate Dir. Clinical Operations as needed with other clinical trial and administrative support activities as assigned.
Minimum 4-year degree in medical, pharmaceutical, or sciences preferred
Good Clinical Practice (GCP) and ICH certification preferred
Knowledge of the pharmaceutical industry and the drug development process
At least 2 years on-site monitoring experience in Clinical R&D