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. 

Responsibilities:

  • 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 jobs@amarexcro.com.

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