Freelance MLR Submissions Specialist

You are the gatekeeper

You’re the guru of all things submissions, and executing them flawlessly truly brings you pride. Your team and clients depend on your ambition to keep a perfect track record. Your eagle eyes spot mistakes before they’re ever allowed to happen, in no small part thanks to your strict adherence to guidelines and your tech savvy. Your checklist is your Rosetta Stone, and with it you make sense of the thorniest submissions with confidence and ease.

Your MLR CM, Copy, and Account partners, and even your clients, are confident you’ll make them look good when their tactics are
scrutinized. You’re skilled at navigating submissions platforms that are often notoriously tricky and can guide others safely past the pitfalls.
But you don’t stop there—you’re always on the lookout for ways to improve the process and enjoy giving your coveted submission checklist
regular tune-ups.

POSITION REQUIREMENTS:
• Bachelor’s degree
• 2+ years of relevant work experience, preferably in science, medicine, or at a pharmaceutical advertising agency
• Ability to thrive and grow in a fast-paced environment
• Extremely detail-oriented and organized approach
• Proficiency in Microsoft Office (Word, Outlook, Excel, PowerPoint) and Adobe Acrobat
• Familiarity with Veeva PromoMats and PubMed

A FOUNDATIONAL SKILL SET DEFINED BY:
• Ability to work collaboratively with multiple departments and levels within the agency
• Strong team-oriented approach and excellent interpersonal skills
• Ability to prioritize deadlines and work under pressure
• A passion for sciences and regulations

• Technological Savvy

Keep it under control

• you will be expected to:
  • Become familiar with client procedures and guidelines on how to successfully submit a job for MLR Review
  • With guidance from MLR Content Managers, create, uphold, and maintain submission checklists per brand
  • In collaboration with Copy, organize references to streamline project submissions 
• you will excel by:
  • being bold in identifying and brave in communicating ways to make submissions more efficient 
  • collaborating with teammates from other departments
  • owning all reference management for your assigned brands

Know your stuff

• you will be expected to:
  • Be an expert on regulations for FDA and OPDP submissions
  • stay current with new electronic submission and regulatry documentation practices and standards
• you will excel by: 
  • actively seeking out training opportunities and industry developments 

Make it seamless

• you will be expected to: 
  • manage multiple submissions and deadlines
  • prepare for submission by:
    • performing QC of submission components prepared by twam prior to submission
    • tagging and linking references
    • fact-checking claims as needed
    • annotating any comments relevant to MLR reviewers prior to submission
  • Press"go" on submissions 
• you will excel by:
  • understanding the needs and challenges of clients 
  • working indepdendently, with minimal supervision 

Omnicom Health Group is committed to hiring and developing exceptional talent. We agree that talent is equally distributed, and we’re focused on developing diverse teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us—we look forward to getting to know you