Coordinator, MLR, Princeton, NJ - Hybrid

Sun Pharmaceutical Industries Ltd•Princeton, NJ

8d•$91,000 - $111,000•Hybrid

About The Position

The MLR Coordinator supports the operational execution of the promotional review process, ensuring that materials are submitted, routed, and tracked accurately within the company’s MLR system. This role partners with cross‑functional teams to maintain documentation, manage workflows, and ensure smooth and compliant review cycles. Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients. As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being.

Requirements

Bachelor’s degree preferred; equivalent experience considered.
1–3 years of experience in administrative coordination, marketing operations, or regulatory/compliance support.
Experience with MLR Committee work and MLR platforms (e.g., Veeva PromoMats) preferred.
Strong organizational and communication skills.
Ability to work efficiently in a fast‑paced environment.
Ability to manage multiple priorities and stakeholders.
Strong attention to detail with a focus on documentation accuracy.
Proficiency in Microsoft Office applications.

Responsibilities

Manage intake, submission, routing and tracking of all promotional and non-promotional materials in the MLR platform (e.g., Veeva PromoMats), ensuring accuracy of metadata, references, and versioning.
Understand and ensure compliance with MLR Standard Operating Procedure.
Ensure submissions are complete, properly tagged, and compliant with required workflows.
Maintain accurate records, version control, and audit documentation.
Facilitate MLR review meetings and track and scribe discussions live via Veeva PromoMats.
Track review progress and proactively follow up with submission owners and reviewers.
Prepare and finalize approved promotional materials for timely routing to Regulatory Affairs for FDA submission.
Prepare reports and dashboards for volume, cycle time, and compliance metrics.
Serve as a point of contact for system and process questions.
Support process documentation and assist with onboarding and training of new system users.
Perform quality checks on content prior to submission to ensure materials meet technical system requirements and include all required documentation.
Maintain detailed audit trails and ensure compliance with internal documentation standards and version‑control procedures.
Coordinate logistics for MLR meetings including scheduling, invitations, agendas, and meeting preparation.
Capture review comments and revisions in the system, ensuring feedback is documented accurately for submission owners.
Serve as the primary liaison between reviewers and submitters to resolve missing information, system issues, and submission errors.
Track deadlines for review cycles, monitoring for delays and escalating issues as needed to ensure timely approvals.
Generate standard and ad hoc reports, including KPIs such as cycle time, volume of submissions, reviewer workload, and material aging.
Assist Marketing and Brand teams with proper format preparation, system tags, submission requirements, and training.
Ensure compliance with archival, expiration, and withdrawal procedures for outdated or superseded materials.
Participate in process improvement discussions and process optimization for workflows, training resources, and job aids.
Partner with IT and Veeva support to troubleshoot system errors and support enhancements.
Other duties as assigned