Senior Medical Editor, MLR & Content Quality

The Blue Venture Fund; Overland Park (KS); On-site; USD 85,000 - 115,000; Full time

Job summary

EVERSANA is seeking an experienced Medical Information/Communications professional to join our Medical Affairs team. The role focuses on producing scientifically rigorous medical content, ensuring accurate data, and maintaining regulatory compliance.

You will review, edit, and validate medical documents, SOPs, and training materials, while supporting MLR readiness and cross-functional collaboration. The position is full-time and home office–based in the United States, with travel as needed.

Qualifications

• Bachelor’s degree in life sciences or pharmaceutical field required.
• Minimum of 2 years of experience in pharmaceutical industry, Medical Information, or Medical Communications with editorial/quality-control exposure.
• Familiarity with MLR review processes and FDA/ICMJE-aligned editorial standards.

Responsibilities

• Support MLR readiness through pre-submission quality checks and reference validation.
• Write and edit medical content related to Medical Affairs, Medical Information, and Medical Communications (SRD, FAQs, slide sets, abstracts, posters, training materials).
• Conduct editorial, language, and scientific accuracy reviews of promotional and non-promotional materials.
• Ensure alignment with FDA guidance, AMA style, and regulatory standards across formats.
• Demonstrate familiarity with Veeva Vault for content review and workflow management.
• Collaborate with writers, MLR coordinators, and reviewers to deliver high-quality outputs on deadlines.
• Mentor junior editors and lead process-improvement initiatives.

Skills

Medical editing

Scientific writing

Quality control

Communication skills

Education

Bachelor’s degree in life sciences or pharmaceutical stream

Tools

Veeva Vault

Job description

EVERSANA is seeking an experienced Medical Information/Communications professional to join our Medical Affairs team. The role focuses on producing scientifically rigorous medical content, ensuring accurate data, and maintaining regulatory compliance.

You will review, edit, and validate medical documents, SOPs, and training materials, while supporting MLR readiness and cross-functional collaboration. The position is full-time and home office–based in the United States, with travel as needed.