22 recruiters in the list
I am a trained clinical research professional, with intensive training in ICH GCP E6 R (2)FDA Regulations, Informed Consent Process, GDP following ALCOA-C principles, Identification and reporting of AEs and SAEs, Comprehension and Execution of Clinical Trial Protocols, Maintaining a regulatory binder and more, Clinical Research, Clinical Research, Georgia, clinical research coordinator, crc, Buford, Buford, Clinical Trials, Clinical Trials