MLR Submission Support Associate – Hybrid (Indianapolis, Indiana, USA)
Location: Indianapolis, Indiana, USA (Hybrid)
Job Type: Full-Time, Regular
Division: Precision AQ
Business Unit: Product Solutions
Experience Required: 0–2 years in project management, data management, or pharmaceutical support functions
Requisition Number: 6298
Company Overview
Precision AQ is a global leader in biopharmaceutical solutions, driving value through analytics, data science, and technology innovation. Our mission is to help patients access the best therapies while enabling healthcare providers to make informed treatment decisions. We value collaboration, precision, and creativity, providing an environment where problem-solvers thrive.
Position Summary
The MLR (Medical, Legal, Regulatory) Submission Support Associate I will support the Delivery Enablement team in managing and creating submission materials for AccessGenius, a market-leading biopharmaceutical access solution. The role focuses on content creation, project coordination, quality control, and stakeholder collaboration to ensure timely and accurate MLR submissions.
This hybrid role requires presence in Indianapolis, Indiana. Sponsorship is not available for this position.
Key Responsibilities
Lead the development and oversight of materials for MLR submissions, client presentations, training, and testing processes.
Manage submissions on MLR platforms including uploads, tagging, linking, and quality checks.
Monitor annotations and ensure adherence to submission best practices and client requirements.
Edit and finalize submission documents and training materials with exceptional attention to detail.
Collaborate with Engagement and MLR teams to manage project timelines, delivery, and product quality.
Provide audit support and deliver MLR training to team members.
Utilize design and content tools such as Adobe Creative Suite (InDesign, Photoshop, Illustrator, XD), Figma, Sketch to support submission processes.
Execute and document manual test cases, track issues, and report project status, risks, and concerns.
Develop knowledge of managed market and payer data to enhance client engagement and operational efficiency.
Support continuous process improvement, balancing speed and quality of deliverables.
Qualifications
Minimum Requirements:
Bachelor’s degree in any relevant field.
Entry-level to 2 years of experience in project management, tool development, or data management.
Strong proficiency in Microsoft Office (Word, Excel, PowerPoint).
Excellent organizational, analytical, and problem-solving skills.
Clear and confident verbal and written communication skills.
Exceptional attention to detail and ability to prioritize multiple tasks.
Preferred Qualifications:
Knowledge of the pharmaceutical marketplace, brands, and healthcare data.
Experience with Adobe Acrobat Pro, Photoshop, Illustrator, InDesign.
Advanced Microsoft Office skills including Excel, Word, and PowerPoint.
Strong time management skills and ability to work with cross-functional teams.
Compensation & Benefits
Estimated Salary Range: $50,000 – $58,000 USD annually (dependent on skills, experience, and location).
Eligible for discretionary annual bonus, health insurance, retirement savings, life insurance, disability benefits, parental leave, and paid time off.
Why Join Us?
Work in a collaborative, innovative, and dynamic environment.
Gain experience in biopharmaceutical commercialization and MLR processes.
Engage in meaningful projects that impact patient access and healthcare outcomes globally.
Note: Beware of fraudulent employment offers. All genuine offers will come through the official recruitment process with our hiring team.
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