Senior MLR Submissions Lead — AI-Driven Compliance

Interpublic

United States

Hybrid

USD 52,000 - 81,000

Full time

14 days+

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Job summary

Omnicom Health Market Access is seeking a Senior Submissions Specialist to drive flawless MLR submissions. You will manage day-to-day submission work, ensuring accuracy, timeliness, and regulatory compliance across brands using Veeva PromoMats and related platforms.

You will mentor teammates, optimize workflows with AI and digital tools, and collaborate with regulatory, content, and operations teams to deliver high-quality outputs for patients and providers.

Qualifications

  • 5+ years in MLR submissions or regulatory operations in healthcare.
  • Experience managing high-volume submissions and digital workflow tools.
  • Mastery of Veeva PromoMats required.
  • Strong organizational and project management abilities.
  • Ability to mentor and develop submissions team members.

Responsibilities

  • Manage, QC, and execute MLR submissions, ensuring accuracy, compliance and on-time delivery.
  • Work within Veeva PromoMats and other platforms to tag/link and execute workflow tasks per brand standards.
  • Utilize digital tools and AI solutions to streamline submission tracking, documentation, and reporting.
  • Troubleshoot and resolve submission issues, identifying opportunities for process improvement.
  • Collaborate with the Senior MLR Operations Manager, content, and regulatory teams to support project delivery.
  • Mentor and support the development of submissions team members.

Skills

MLR submissions
Veeva PromoMats
AI tools
Regulatory operations
Project management
Troubleshooting

Tools

Veeva PromoMats
Digital platforms

Job description

Omnicom Health Market Access is seeking a Senior Submissions Specialist to drive flawless MLR submissions. You will manage day-to-day submission work, ensuring accuracy, timeliness, and regulatory compliance across brands using Veeva PromoMats and related platforms.

You will mentor teammates, optimize workflows with AI and digital tools, and collaborate with regulatory, content, and operations teams to deliver high-quality outputs for patients and providers.

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