CMLR Coordinator

Praxis Precision Medicines, Inc.

$100K — $120K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Proven experience in coordinating MLR review workflows across diverse teams.
  • Strong knowledge of regulatory and compliance guidelines relevant to promotional materials.
  • Experience managing timelines and documentation in specialized MLR systems.
  • Ability to facilitate meetings and drive team alignment on project approvals.
  • Demonstrated skill in identifying process bottlenecks and implementing improvements.
  • Proven ability to train and onboard stakeholders on complex processes and systems.
  • Excellent communication skills to articulate project risks and status updates.

Responsibilities

  • Coordinate end-to-end MLR review workflows for various materials.
  • Manage timelines, approvals, and documentation within MLR platforms.
  • Partner with key teams to ensure compliant review processes.
  • Facilitate MLR meetings and track feedback and action items.
  • Identify and recommend improvements for workflow efficiency.
  • Ensure maintenance of accurate review records and documentation.
  • Support training and onboarding for internal stakeholders and partners.
  • Serve as a proactive operational partner in communication.

Benefits

  • 99% premium coverage for medical, dental, and vision plans.
  • Company-paid life insurance and disability benefits.
  • 401(k) matching up to 6% and long-term stock incentives.
  • Discretionary quarterly bonuses.
  • Flexible wellness benefit supporting personal health initiatives.
  • Generous PTO, paid holidays, and company-wide shutdowns.
  • Collaborative and inspiring workplace culture.
Full Job Description
Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed.

Primary Responsibilities
  • Coordinate end-to-end MLR review workflows for promotional, educational, and corporate materials across multiple functions and stakeholders
  • Manage review timelines, approvals, version control, documentation, and routing within MLR systems and platforms
  • Partner with Commercial, Medical, Regulatory, Legal, and Compliance teams to ensure timely and compliant review processes
  • Facilitate MLR meetings, capture feedback, track action items, and drive alignment toward final approvals
  • Identify workflow bottlenecks and recommend process improvements that increase efficiency, transparency, and accountability
  • Ensure accurate maintenance of review records, archives, and audit-ready documentation in accordance with company policies and regulatory requirements
  • Support training and onboarding for internal stakeholders and agency partners on MLR processes, systems, and best practices
  • Serve as a reliable operational partner who proactively communicates risks, status updates, and timeline changes

Qualifications and Key Success Factors
  • Coordinate end-to-end MLR review workflows for promotional, educational, and corporate materials across multiple functions and stakeholders
  • Manage review timelines, approvals, version control, documentation, and routing within MLR systems and platforms
  • Partner with Commercial, Medical, Regulatory, Legal, and Compliance teams to ensure timely and compliant review processes
  • Facilitate MLR meetings, capture feedback, track action items, and drive alignment toward final approvals
  • Identify workflow bottlenecks and recommend process improvements that increase efficiency, transparency, and accountability
  • Ensure accurate maintenance of review records, archives, and audit-ready documentation in accordance with company policies and regulatory requirements
  • Support training and onboarding for internal stakeholders and agency partners on MLR processes, systems, and best practices
  • Serve as a reliable operational partner who proactively communicates risks, status updates, and timeline changes

The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.

Compensation & Benefits

At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let's achieve the impossible together!

To round out our world-class total rewards package, we provide annualized base salary compensation in the range listed below. This range reflects the base salary the Company reasonably expects to pay for the position at the time of posting. Placement within the range will be based on job-related factors, including experience, qualifications, scope of responsibilities, and demonstrated track record of delivering results in similar roles.

Annualized Base Salary

$100,000-$120,000 USD

Similar Jobs

More Jobs at Praxis Precision Medicines, Inc.

More Pharmaceuticals & Biotech Jobs

Find similar CMLR Coordinator jobs: