Qualified candidates must reside in Metro Atlanta, GA
SUMMARY
The Medical Information Specialist (MIS) is responsible for handling medical information, adverse events and/or product complaints on behalf of TMAC clients. The MIS will be trained in policies and procedures in accordance with FDA regulations as it relates to medical information, drug safety /surveillance, pharmacovigilance and product quality. The MIS is expected to develop a high level of expertise in these areas and is continuously aware of changes in these regulations.
The MIS will be trained in various disease states and products and be expected to maintain a high level of expertise in these areas as they relate to the daily activities of TMAC clients. In addition, the MIS will establish a high level of working knowledge about TMAC’s medical information databases. As requested, the MIS will contribute to development and set up of projects relating to programs within all departments at TMAC.
ESSENTIAL DUTIES AND RESPONSIBILITIES
QUALIFICATIONS
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