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Medical Reviewer/Safety Reviewer
2 weeks ago
Contract
Columbus, Ohio, US

Job Description

To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you!

 

Job description:

  • Responsibilities include medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, 
  • QA of data listings. 
  • May manage the activities of regional contract CRAs, and organizes the files and budgets associated with several clinical studies. 
  • Provides medical support which may include: Adverse Event Reporting - the investigation and reporting of medical product experiences, in depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; or Medical Communication which includes writing standard and custom responses to communication requests, in-depth assistance to the medical and lay community by responding to inquiries with medical/scientific information that is more complex and requires more data than is supplied in the package insert or the standard letter database.
  • May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and CRF completion, writing study summaries, and review protocols, study summary investigator brochures and IND annual updates for safety data verification. 
  • 0-3 Years' Experience Level.

 

Job Requirements

Medical Reviewer, Safety Reviewer , Case Report Forms , CRFs, Adverse Event Reporting, medical product, FDA, IND , CRF , Pharma , Pharmaceuticals , Medical Device

 

Job Code: 50254292

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Recruiter Chitrank
Email
Phone +4255231648