Medical Content and Review Specialist

. Manages the end-to-end MLR process .

Posted 4/8/2026full-timeRemote • 🇮🇳 IndiaJuniorMid-LevelWebsite

Tools & technologies

Vault

Key responsibilities & impact

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

What you’ll need

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.

Comp & perks

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Scientific WritingScientific ReviewingMLRFDA 2253 submissions

Soft Skills

Time managementMeeting managementCustomer serviceEffective communication