Alliance Research Group is seeking a full time staff member to serve as the regulatory specialist for prospective and ongoing clinical trials. We are looking for someone with excellent computer and office skills to support a small group of clinical research study coordinators in the psychiatric field. This position includes performing administrative tasks, daily data entry, scheduling, completing study start-up documents, accomplishing tasks at sponsor and CRO's request and maintaining the site's regulatory documents and correspondence. Candidates must be organized, flexible, and ready to adapt to a fast paced company. Clinical Research Experience Preferred. 

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