Regulatory Affairs Specialist - Bethesda - job 1197371

Technical Resources International, Inc.

Date: 09/12/2021

City: Bethesda, Maryland

Employment type: Full-time


Responsibilities:



  • Prepare, distribute and track Investigational New Drug Applications (INDs)

  • Prepare FDA required IND sponsor’s annual reports

  • Prepare scientific and other regulatory documents for submission to the Food and Drug Administration (FDA)

  • Attend scientific meetings and reviews the literature to stay current with new developments in the infections disease field (in particular, human immunodeficiency virus (HIV) and tuberculosis (TB) and therapeutic clinical research

  • Preparation of investigator/pharmaceutical company meeting minutes

  • Perform literature searched and extraction of information to support regulatory documents



Recommended Skills


Toxicology

Molecular Biology

Pharmaceuticals

Diseases And Disorders

Drug Administration

Tuberculosis Management



Job Snapshot

Employee Type


Full-Time

Location


Bethesda, MD

Job Type


Biotech

Experience


Not Specified

Date Posted


08/18/2021

Job ID


59/32/127




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