Clinical Research Associate/Monitor

Looking for CRA's / Monitor in the following areas:

1) Philadelphia

2) New York City (Boston, Stoneybrook, Brooklyn, Staten Island)

3) Chicago, Detroit or Indianapolis

4) Los Angeles

 

Responsibilities:Coordinate study start-up activities, including protocol preparation, CRF design, essential document review and approval, investigator selection etc. Monitoring study site activities through frequent on-site visits and telephone contacts to assure compliance with protocols, applicable SOPs, ICH GCP guidelines and government regulations.Coordinate study close-down activities, including data cleanup, clinical study report writing, generation of scientific publication Prepare and submit written reports and correspondence in a timely, concise, and accurate manner

 

Qualifications:Bachelor's degree and 2+ years of clinical research and monitoring experience required.  RN preferred.  Solid understanding of ICH/GCP regulationHighly organized with excellent verbal and written communcation skills.  Must be willing to travel more than 50%