EVERSANA

Medical Content and Review Specialist

EVERSANA

full-time

Posted on:

Location Type: Remote

Location: India

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About the role

  • Manages the end-to-end MLR process
  • Responsible for scheduling, setting the agenda, and leading Review Committee meetings
  • Add live discussion notes for comments discussed in Veeva Vault Scribe meeting minutes
  • Ensure all covered communications are properly vetted through the review process
  • Verifies that materials are assigned to the appropriate review path
  • Rejects incomplete submissions and materials that are not review ready
  • Supports FDA 2253 submissions with MLR Regulatory Reviewer/Partner

Requirements

  • Graduates in any Life Sciences / Biomedical field
  • At least 2 years of experience in a healthcare agency or pharmaceutical company
  • Experience with use of Veeva Vault PromoMats / MedComms
  • Experience in Scientific Writing / Scientific Reviewing / MLR
  • Time management
  • Meeting management
  • Excellent customer service skills
  • Must demonstrate excellent ability to communicate effectively in English, both orally and in writing.
Benefits
  • Medical insurance
  • Remote work options
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
Scientific WritingScientific ReviewingMLRFDA 2253 submissions
Soft Skills
Time managementMeeting managementCustomer serviceEffective communication