The Clinical Research Associate (CRA) II is a key participant in the implementation and monitoring of clinical trials. Participates in recruitment/selection of new investigators, investigative sites, and outside vendors.
Under minimal supervision, the CRA II displays clinical trial and vendor management experience in the planning, designing, implementation and execution of clinical trial protocols. Works closely with site(s) and vendors to ensure compliance with overall clinical and protocol objectives. Assists in the planning and implementing activities required to conduct and monitor clinical trials and ensures that Good Clinical Practices (GCP) are followed. Monitors investigator performance and adherence to protocol, and proactively addresses conduct issues and enrollment problems, as necessary. Assists in preparation of presentations of scientific meetings and technical discussions.
ESSENTIAL JOB FUNCTIONS: