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Medical Content And Review Specialist (Us Hours)

2+ years
Not Disclosed
10 June 27, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Medical Content & Review Specialist (Remote – US Hours)

Job Summary:
EVERSANA is seeking a highly organized and detail-oriented Medical Content & Review Specialist to join our Medical, Legal, and Regulatory (MLR) team. In this fully remote, full-time position, you will manage end-to-end MLR processes, lead review meetings, and ensure compliance with industry regulations using tools like Veeva Vault PromoMats. Ideal for candidates with 2+ years of experience in healthcare agency or pharma settings, this role supports top-tier medical content development across US hours from locations such as Poland, Germany, Ireland, the UK, Portugal, Italy, or Spain.


Key Responsibilities

  • Manage the end-to-end MLR process, including scheduling and leading review committee meetings

  • Scribe meeting minutes, draft and finalize them post-approval

  • Add live comments during meetings in Veeva Vault

  • QC final content versus approved versions

  • Coordinate upload and annotation of materials into clients' approval platforms

  • Maintain compliance with global healthcare promotion regulations

  • Support development of SOPs and project plans in Medical Affairs and Medical Information

  • Ensure consistent documentation and process improvement metrics

  • Communicate effectively with cross-functional stakeholders


Required Skills & Qualifications

  • Bachelor's degree in Life Sciences, Biomedical Sciences, or a related healthcare field

  • Minimum 2 years of experience in pharmaceutical or medical communications agency settings

  • Hands-on experience with Veeva Vault PromoMats/MedComms

  • Proficiency in project and meeting management

  • Excellent written and spoken English communication skills

  • Strong attention to detail and organizational ability

  • Customer service orientation with a commitment to quality

  • Experience in scientific writing, reviewing, and content QC

  • Ability to work flexible hours aligned to US time zones


Preferred Qualifications

  • Postgraduate degrees (Pharmacy, Medicine, or related fields)

  • Understanding of global promotional compliance requirements

  • Knowledge of US FDA advertising and drug/device promotion laws

  • Familiarity with medical terminology

  • Competence with MS Office Suite (Outlook, Word, Excel, PowerPoint)


Perks & Benefits

  • Fully remote work from anywhere in eligible European countries

  • Flexible US working hours

  • Inclusive and diverse work culture

  • Career development opportunities

  • Exposure to global healthcare clients

  • Engaging and collaborative team environment

  • Mission-driven company supporting patient health globally


About EVERSANA

EVERSANA is a global leader in next-generation commercialization services for the life sciences industry. With over 7,000 employees worldwide, we support over 650 clients including biotech start-ups and established pharmaceutical companies. Our integrated services and technology solutions bring innovative therapies to market and support patients worldwide.


Work Mode: Remote (US business hours, full-time, 9-hour shifts between 2 PM – 2 AM CET)


Call to Action

Ready to help shape the future of healthcare communications? Apply today to join EVERSANA as a Medical Content & Review Specialist and bring your medical writing and MLR expertise to a patient-centered team that makes a real impact.