The candidate for this position must have a firm knowledge of the regulatory and clinical aspects of running a clinical trial. Candidate will be responsible for all communications with the sponsoring company, managing study patient files, enrollment logs and study related procedures. Candidate will be responsible for patient recruitment with the help of the office staff and the office M.D's. Candidate must make sure that all study logs are up to date and all instrument calibrations are done. GCP knowledge is a must.
Candidate must posses good personal skills as well as strict attention to detail.
Job Type: Full-time
Pay: $22.00 - $30.00 per hour
