Internship Program: Safety & Pharmacovigilance


Position Summary: The Safety Intern assists the Safety & Pharmacovigilance designees with prompt and accurate processing of Serious Adverse Events (SAEs), preparation of safety narratives for clinical trial patients, and medical coding of adverse events and concomitant medication terms. 


  • Management of Safety related faxes/emails for assigned Studies

  • Enter incoming safety events into Study-related Safety Tracking Systems and databases

  • Process expedited/non-expedited safety events based on Medical Monitor’s evaluation in accordance with company’s SOPs and other regulatory guidelines

  • Provide administrative support for the Safety Department, if required

  • Assist with medical coding of adverse events and concomitant medications and any other applicable term according to the Scope of Work

  • Assist with narrative writing under supervision of the Study’s Medical Monitor

Required Education, Qualifications and Experience:

  • RN, Associate’s or Bachelor’s degree in scientific, nursing or medical curriculum

  • Competent in the use of Microsoft Office software

  • Understanding of medical terminology

  • Strong problem solving and decision making skills

  • Strong oral communication skills

  • Must present documents showing legal authorization to work in the U.S.

To submit your CV for our consideration, please email us at

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