MLR Submission Support Associate I (Copywriter, Paralegal, Professional Writer)

***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.***

Do you have a Copywriter, Paralegal, Teacher, or professional writing background?  If so, this is the perfect job for you!

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