Instagram
youtube
Facebook

Medical Content And Review Specialist

2 years years
Not Disclosed
10 Aug. 26, 2025
Job Description
Job Type: Remote Education: Bachelor's or advanced degree in Life Sciences, Biomedical Sciences, or a related field 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

Job Title: Medical Content and Review Specialist

Department: Clinical & Medical
Job Family: Medical Writing
Employment Type: Full-time
Location: Remote (Work from Home)


Company Overview

EVERSANA is a global leader in next-generation commercialization services for the life sciences industry. With more than 7,000 employees worldwide, we support 650+ clients—from biotech startups to large pharmaceutical firms—in bringing therapies to market and improving patient outcomes.

At EVERSANA, we:

  • Celebrate diversity and promote inclusion

  • Operate based on a set of Cultural Beliefs focused on patient-centricity, innovation, collaboration, and client satisfaction

  • Have been consistently recognized as a Great Place to Work globally


Position Overview

As a Medical Content and Review Specialist, you will manage the Medical, Legal, and Regulatory (MLR) review process for a dedicated client, ensuring that promotional and non-promotional content is accurate, compliant, and publication-ready. You will work with tools like Veeva Vault PromoMats and MedComms, facilitate live review meetings, ensure quality control, and support the development of compliant medical content.


Key Responsibilities

MLR Review Management

  • Manage the end-to-end MLR process

  • Schedule and lead Review Committee meetings

  • Take and circulate meeting minutes and ensure final approval and archiving

  • Facilitate live discussions and document reviewer comments in Veeva Vault

  • Ensure completeness and accuracy of submissions

  • Verify correct review path assignment

  • Reject and return incomplete or non-compliant submissions

  • Conduct quality control checks on final versus approved documents

  • Assist with FDA 2253 submissions in collaboration with MLR Regulatory Reviewer

Medical Content Support

  • Assist in developing project plans

  • Provide support to the Medical Content Development Team

  • Upload and annotate materials in client platforms (e.g., Veeva Vault), including anchoring references

Medical Affairs & Medical Information Support

  • Collaborate with leadership to manage project plans and timelines for medical initiatives

Additional Duties

  • Perform all other responsibilities as assigned

  • Ensure compliance with internal standards and regulatory policies

  • Provide exceptional client service and contribute to overall project excellence


Required Qualifications

Education

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

Experience

  • Minimum 2 years of experience in:

    • Healthcare communications, medical writing, or scientific review

    • MLR process in a pharmaceutical company or healthcare agency

    • Using Veeva Vault PromoMats / MedComms for content review

    • Project and meeting management, including organizing agendas and leading discussions

Skills

  • Strong written and verbal communication in English

  • Ability to work independently with a high level of attention to detail

  • Exceptional time management, organization, and customer service skills

  • Familiarity with FDA guidelines and industry standards for promotional content

  • Proficiency in Microsoft Office (Word, PowerPoint, Excel, Outlook)


Desirable Attributes

  • Proactive, collaborative, and flexible

  • Able to adapt quickly in a fast-paced, matrixed environment

  • Strong problem-solving and critical thinking skills

  • High level of professional integrity and ethical behavior


Work Environment and Culture

EVERSANA fosters a collaborative, inclusive, and empowering work culture where each employee plays a role in improving patient lives. We encourage our team to embrace our Cultural Beliefs:

  • Patient Minded – Prioritize the patient in all decisions

  • Client Delight – Own each client interaction and its outcome

  • Take Action – Act with confidence and urgency

  • Grow Talent – Invest in personal and team development

  • Win Together – Collaborate across functions for success

  • Communication Matters – Encourage open, honest dialogue

  • Embrace Diversity – Celebrate all backgrounds and perspectives

  • Always Innovate – Pursue bold and creative ideas


Equal Opportunity Employer

EVERSANA is committed to diversity, equity, and inclusion in the workplace. We are proud to be an Equal Opportunity Employer, welcoming applicants from all backgrounds, regardless of race, gender identity, age, religion, disability, veteran status, sexual orientation, or any other identity.


Important Notice

EVERSANA is aware of fraudulent job offers impersonating our brand. Please note:

  • We never request payment or sensitive personal information during hiring

  • All communication will be from official EVERSANA channels


Connect With Us

Follow us to learn more: