Med Regulatory Specialist: Research for medical drug development, coordinate & document regulatory processes in clinical trials for FDA approval, prepare, collect, compile regulatory docs, & process submission to regulatory authorities, Manage collection, review & approval of regulatory docs from clinical sites & ensures ongoing maintenance of records, medical writings & biostats, Ensure integrity of clinical data in adherence to all applicable regulatory guidelines.
Requires Master's degree in Health Science, Biotech, or related.
Job location: M&K Biosciences Inc in Gaithersburg, MD. Send resume with cover letter to M&K Biosciences Inc, 25 W Watkins Mill Rd #C, Gaithersburg, MD 20878, Attn: Dr. LEE for interview.
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