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EVERSANA INTOUCH®

Medical, Legal and Regulatory (MLR) Coordinator

RemoteUnited States only
Published
Role
Project Management
Experience
Mid
Employment
Contract
Company size
Enterprise
Salary not disclosed
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Open to US only. Set where you work from to check your eligibility.

No BS summary

Medical/legal/regulatory review coordinator for healthcare marketing, with 2+ years in a healthcare agency or pharmaceutical company. Needs Life Sciences/Biomedical education, English communication, Veeva Vault PromoMats/MedComms, and MLR/scientific writing or reviewing experience. Full-time role in Overland Park, KS.

Core skills

Veeva Vault PromoMatsVeeva Vault MedComms

Required skills

OutlookMicrosoft OfficeMicrosoft WordMicrosoft ExcelMicrosoft PowerPoint

Required languages

English excellent ability to communicate effectively, both orally and in writing / requiredFull-time role in Overland Park, KS, United States. Onsite Office work environment described; US-specific ADA and compensation language. Benefits are referenced; no remote/worldwide language.

What you'll do

  • Manages the end-to-end MLR process.
  • Responsible for scheduling, setting the agenda, and leading Review Committee meetings.
  • Add live discussion notes for comments discussed in Veeva Vault Scribe meeting minutes, circulate draft meeting minutes for Committee approval and finalize and file approved minutes.
  • Ensure all covered communications are properly vetted through the review process utilizing the online review system (e.g., Veeva Vault PromoMats and Vault MedComms).
  • Cascade and enforce any new policies and guidelines related to review of materials.
  • Verifies that materials are assigned to the appropriate review path.
  • Rejects incomplete submissions and materials that are not review ready.
  • Facilitates/documents discussion in live meetings.
  • QCs Final Document vs. Approved Document.
  • Supports FDA 2253 submissions, or country specific regulatory submissions with MLR Regulatory Reviewer/Partner.
  • Support the development of project plans.
  • Support medical content development team.
  • Support upload of materials into clients’ review and approval platforms, including supporting annotating, anchoring references, etc.
  • Support Medical Affairs and Medical Information leadership in developing and managing project plans for key initiatives.
  • Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias.
  • All other duties as assigned.
  • Maintain and contribute toward process improvement which positively impacts metrics associated with activities of the MLR Review process; metrics are subject to change annually or more often as deemed necessary.
  • Maintain and improve customer services associated with the activity of the MLR review.
  • Complete MLR coordination responsibilities in a timely manner.

What they require

  • Able to work full-time and be flexible with work scheduling as required by clients and management.
  • Graduates in any Life Sciences / Biomedical field.
  • Must demonstrate excellent ability to communicate effectively in English, both orally and in writing.
  • At least 2 years of experience in a healthcare agency or pharmaceutical company.
  • Experience with use of Veeva Vault PromoMats / MedComms.
  • Experience in Scientific Writing / Scientific Reviewing / MLR Project management.
  • Time management.
  • Meeting management.
  • Excellent customer service skills.
  • Computer proficiency in Outlook and Microsoft Office Suite (Word, Excel, PowerPoint, and other Window applications).
  • Preferred: Graduates/Postgraduates in Pharmacy or Medicine preferred.
  • Preferred: Working knowledge of or familiarity with global healthcare compliance statutes and laws.
  • Preferred: Ability to perform assignments with a high degree of independence requiring extensive experience, skill, and knowledge.
  • Preferred: Excellent computer skills including competency in presentation, word processing and spreadsheet software, utilizing MS Office Suite.
  • Preferred: Proven ability to manage multiple tasks, set priorities and meet deadlines.
  • Preferred: Ability to manage cross-functional projects.
  • Preferred: Familiar with laws and regulations regarding US drug / device advertising and promotion, including industry best practices.
  • Preferred: Knowledge of medical terminology (preferred but not required).
  • Must be quality-oriented and demonstrate consistent attention to detail.
  • Must have the ability to follow established processes and procedures and the flexibility to adopt new practices and priorities as required.
  • Positive Attitude and Energy – Exhibits an upbeat attitude, a genuine interest in others and a sense of humor. Energizes others and heightens morale through her/his attitude.
  • Communication Skills – Possesses the ability to develop and articulate ideas and information that generate understanding and create a climate that motivates and encourages others to participate.
  • Innovator – Transforms creative ideas into original solutions that positively impact the company’s performance.
  • Highly Principled – Proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior.
  • While performing the essential functions of this job the employee is frequently required to reach, grasp, stand and/or sit for long periods of time (up to 90% of the shift), walk, talk and hear; occasionally required to lift and/or move up to 25 pounds.

Benefits

  • EVERSANA is committed to providing competitive salaries and benefits for all employees.
  • More information about EVERSANA’s benefits package can be found at eversana.com/careers.

EVERSANA INTOUCH® is a global, full-service marketing agency network serving the life sciences industry and part of a fully integrated commercialization platform through EVERSANA®. It provides next-generation creative and media services, enterprise solutions and data analytics services for clients.

🇺🇸 United StatesHealthcareEnterprise

What people say about this company

3.0/ 5

Salary not disclosed