Healthcare MLR Coordinator - Compliance & Content Oversight

Eversana; United States; Sur place; USD 65 000 - 85 000; Plein temps

Résumé du poste

EVERSANA is seeking an MLR Coordinator to manage end-to-end medical, legal and regulatory review processes for a dedicated client. You will schedule and lead review meetings, document discussions, and ensure compliance with internal policies and external regulations.

The role supports medical content projects, regulatory submissions, and cross-functional collaboration with Medical Affairs. Strong English communication and 2+ years in pharma are required.

Qualifications

• Graduates in any Life Sciences / Biomedical field.
• Excellent ability to communicate effectively in English, both orally and in writing.
• At least 2 years of experience in a healthcare agency or pharmaceutical company.
• Experience with Veeva Vault PromoMats / MedComms.
• Experience in Scientific Writing / Scientific Reviewing / MLR.
• Project management, time management, and meeting management skills.
• Excellent customer service skills and computer proficiency (Outlook, MS Office).

Responsabilités

• Manages the end-to-end MLR process.
• Schedule, set agenda, and lead Review Committee meetings.
• Add live discussion notes for comments in Veeva Vault.
• Scribe meeting minutes and circulate for approval.
• Ensure materials are vetted through the review process.
• Enforce new policies related to review of materials.
• Support FDA 2253 submissions and country-specific regulatory submissions.

Connaissances

Project management

Time management

Meeting management

Customer service

English communication

Formation

Bachelor's in Life Sciences

Pharmacy/Medicine (preferred)

Outils

Veeva Vault PromoMats

MS Office

Outlook

Description du poste

EVERSANA is seeking an MLR Coordinator to manage end-to-end medical, legal and regulatory review processes for a dedicated client. You will schedule and lead review meetings, document discussions, and ensure compliance with internal policies and external regulations.

The role supports medical content projects, regulatory submissions, and cross-functional collaboration with Medical Affairs. Strong English communication and 2+ years in pharma are required.