Clinical Trials & Surveys Corp. (C-TASC), an independent research organization, is searching for a Clinical Research Associate with extensive experience in coordinating Phase II and Phase III investigational drug and/or behavior therapy trials with knowledge of GCP, ICH, HIPPA privacy rules, and DHHS assurances.  Knowledge of FDA regulations and experience monitoring clinical study sites is also required.  Depending on the study, the position would involve 0 -30 % travel to clinical sites to perform site initiation, monitoring and close-out visits.  PLEASE NOTE THAT THIS IS NOT A HOME-BASED POSITION.  Other duties include participation in conference calls and committee meetings with minute preparation.  Also, employee will serve as liaison with study sites and help with publication development.  The successful applicant should have good writing skills and should possess the knowledge to assist in writing protocols, informed consent forms, and manuals of operations in the field of drug abuse.  Experience filing and maintaining INDs, and reviewing regulatory documents.  Must show proof of CRA certification