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Director, Medical, Legal Regulatory; MLR) Operations

Job in Concord, Middlesex County, Massachusetts, 01742, USA
Listing for: ITF Therapeutics LLC
Full Time position
Listed on 2026-10-21
Job specializations:
  • Business
    Regulatory Compliance Specialist, Change Management
Salary/Wage Range or Industry Benchmark: 210000 - 225000 USD Yearly USD 210000.00 225000.00 YEAR
Job Description & How to Apply Below
Position: Director, Medical, Legal, & Regulatory (MLR) Operations
Reports To:

Sr. Director, Sales Training & Commercial Effectiveness

About This Role:

The Director, MLR Operations owns the strategy, governance, and end-to-end operation of the Medical, Legal, Regulatory review process for the organization. This role ensures all promotional, medical, training, and other regulated materials move through review and approval accurately, compliantly, and on time. Beyond process execution, this person is the strategic owner of the MLR operating model - designing scalable workflows, setting governance standards, and serving as a trusted advisor to senior Medical, Legal, Regulatory, and Commercial leadership.

Success requires professional assertiveness to hold senior stakeholders accountable, sound judgment to balance speed to balance business urgency, review capacity, and process requirements while ensuring compliance risks are surfaced to appropriate functional decision makers. The Director is accountable for the effectiveness, integrity and operational performance of the MLR process, while Medical, Legal, Regulatory and Compliance functions retain accountability for their respective substantive review decisions.

What You'll Do:

Strategic Process Ownership

  • Own the MLR operating model end-to-end - intake, routing, review cycles, approvals, and archiving - and continuously evolve it as volume, therapeutic areas, and regulatory expectations change
  • Set governance standards, SOPs, and best practices for the review process, and ensure consistent adoption across Medical, Legal, Regulatory, and Marketing
  • Serve as business owner for the technology ecosystem (e.g., Veeva Vault Promo Mats), partnering with IT/Compliance on configuration, upgrades, and process automation opportunities
  • Identify systemic bottlenecks and lead cross-functional process improvement initiatives, using data to justify changes to senior stakeholders

Planning, Prioritization & Delivery

  • Build and maintain enterprise-wide review calendars across teams, launches, and material types (promotional, training, medical, and other)
  • Lead MLR operational readiness for new product launches, indications, label changes, and other high-volume business events, including submission volume forecasting, reviewer capacity planning, critical path calendars and escalation protocols.

Cross-Functional Leadership & Influence

  • Serve as the primary strategic point of coordination between Medical, Legal, Regulatory, Marketing, and Commercial leadership on all review matters
  • Facilitate and, where needed, redesign MLR review governance meetings to drive efficient, decisive outcomes among senior reviewers
  • Establish and reinforce clear roles, service-level expectations, timelines, and escalation protocols across reviewer functions and organizational levels; constructively address deviations that put quality, compliance, or business timelines at risk.
  • Build credibility and trusted-advisor relationships across the matrix; influence decisions and behavior change without direct authority
  • Proactively elevate risks to timelines or compliance with clear, data-backed rationale and recommended solutions, not just flagged problems
  • Role-based training and onboarding for material owners, reviewers, agencies and other stakeholders.
  • Establish company requirements for submissions and approvals for external agencies and partners to adhere to.

Reporting, Compliance & Continuous Improvement

  • Define and maintain a MLR performance framework including submission volume, cycle time, SLA adherence, review rounds, aging, etc. Translate insights into capacity plans, process improvements and leadership recommendations.
  • Ensure audit- and inspection readiness through accurate, well-governed review documentation and records retention
  • Stay current on evolving FDA, OPDP, and PhRMA Code expectations and partner with regulatory, legal, and compliance to translate evolving regulatory requirements, guidance, internal policies and enforcement trends into MLR process
  • May mentor or oversee junior process coordinators supporting the MLR function

Who You Are:

You are a strategic and highly organized MLR operations leader who thrives at the intersection of compliance, process excellence, and business execution. You bring deep experience managing complex promotional review environments and have a proven ability to design scalable processes that balance speed, quality, and regulatory rigor. Known for your executive presence and professional assertiveness, you are comfortable influencing senior stakeholders, driving…

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