Medical, Legal and Regulatory (MLR) Coordinator - Remote

Overview

The Medical, Legal and Regulatory (MLR) Coordinator is responsible for managing the MLR processes for a dedicated client, ensuring compliance and effective operation of all administrative and program management support.

In Short

• Manage the end-to-end MLR process.
• Schedule and lead Review Committee meetings.
• Document and circulate meeting minutes.
• Ensure materials are properly vetted through the review process.
• Support FDA submissions and regulatory compliance.
• Assist in medical content development and project plans.
• Support Medical Affairs and Information leadership.
• Demonstrate a commitment to diversity and inclusion.
• Maintain customer service standards.
• Complete responsibilities in a timely manner.

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.
• Strong communication skills in English.
• Proficient in Microsoft Office Suite.
• Excellent customer service skills.
• Project management and time management experience.
• Ability to manage multiple tasks and meet deadlines.
• Knowledge of medical terminology is preferred.
• Strong attention to detail and quality orientation.

Benefits

• Competitive salaries and benefits.
• Inclusive workplace culture.
• Opportunities for professional development.
• Commitment to diversity, equity, and inclusion.
• Supportive work environment.