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Medical, Legal and Regulatory (MLR) Coordinator

📅 Jun 29
MLR Process ManagementProject ManagementTime ManagementMeeting Management

📜 Description

  • Manages the end-to-end MLR process.
  • Schedules and leads Review Committee meetings.
  • Ensures all communications are vetted through the review process.
  • Verifies materials are assigned to the appropriate review path.
  • Supports FDA submissions and project plans.

🛠️ Requirements

  • Graduates in any Life Sciences / Biomedical field.
  • At least 2 years of experience in a healthcare agency or pharmaceutical company.
  • Experience with Veeva Vault PromoMats / MedComms.
  • Strong communication skills in English, both orally and in writing.
  • Excellent customer service skills.

Benefits

  • Support Medical Affairs and Medical Information leadership in developing and managing project plans for key initiatives
  • Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively
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