MLR (Medical, Legal, Review) Submissions Support Associate I

Company: Precision Medicine Group
Location: Indianapolis
Posted on: April 18, 2024

Job Description:

MLR (Medical, Legal, Review) Submissions Support Associate I
at Precision Medicine Group (View all jobs)
Indianapolis, IN, USA

***This role requires you to be located in Indianapolis, Indiana because this is a hybrid role.**

***Unfortunately, we are not able to provide sponsorship now or anytime in the future.***

PRECISIONxtract, part of Precision Value & Health, accelerates value realization by enabling data science, leveraging analytics, and innovating with technology to transform the way you connect with customers. Is helping patients get the best medicine important to you? Is enabling healthcare providers to make appropriate treatment decisions important to you? Are you detail oriented and passionate about organization? Are you a clear and confident communicator? Do you thrive within a team and company that is highly collaborative? Your dream job is waiting. If you're a born problem-solver and enjoy when no day is the same - keep reading.

The MLR (Medical Legal Review) Submission Support Associate I is responsible for the successful creation and oversight of submission materials through MLR processes. The MLR Associate I is a member of the Delivery Enablement team and plays an important role in the delivery of our AccessGenius solution. AccessGenius is our best-in-class market access pull-through solutions for our biopharmaceutical clients. In this role, you will leverage your expertise in a variety of areas including submission support, UX design, project management, organization, communication, critical thinking, and biopharmaceutical commercialization. You will work closely with other teams to create and modify materials for review and approval.

Essential functions of the job include but are not limited to:

• Spearhead content creation for Medical, Legal, Regulatory (MRL) submissions, client presentations, training materials and testing processes.
• Demonstrate knowledge of all MLR platforms utilized by clients.
• Assist with uploads, tagging/ linking and trafficking submissions on an ongoing basis.
• Monitor annotations to ensure that best-practices and submission requirements are followed across teams.
• Manage process of editing submission documents and training materials with attention to detail.
• Coordinate with Engagement teams and across MLR team members to manage work across the submission process including managing delivery timing and product quality.
• Provide audit support and MLR training to Delivery Enablement team members.
• Leverage Adobe Creative Suite - (InDesign, Photoshop, XD, Illustrator), Figma, Sketch to create designs for submission process.
• Execute manual test cases and document results.
• Report status, concerns, and risks for client deliverables including applications, reports, and data files.
• Maintain quality of work, looking for ways to drive improvements while working quickly and efficiently, while delivering a great end product.
• Develop understanding of manage market and payer data to improve client engagement and project management capabilities.
• Travel Expectations up to 15%
  Qualifications:
  
  Minimum Required:
  
  • Bachelor's degree
  • Entry level-2 years working in project management, tool development, and data management
    Other Required:
    
    • Strong collaboration skills, with ability to communicate ideas and concepts
    • High ability with Microsoft Office products including Excel and Work
    • Excellent organizational and problem-solving skills
    • Excellent oral and written communication skills
    • Exceptional attention to detail
      Preferred Skills:
      
      • Working knowledge of pharmaceutical marketplace, brands, and data inputs
      • Illustrator, Adobe Acrobat Pro, Adobe Photoshop, Adobe InDesign
      • Advance knowledge of MS Word, MS PowerPoint and MS Excel
      • Excellent time management skills
        
        Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
        
        Reasonable estimate of the current range
        
        $46,000 - $65,000 USD
        
        Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice .
        
        Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. - 2020 Precision Medicine Group, LLC
        
        If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com .

Keywords: Precision Medicine Group, Lawrence , MLR (Medical, Legal, Review) Submissions Support Associate I, Legal , Indianapolis, Indiana