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Medical And Scientific Reviewer

2+ years years
Not Disclosed
10 Aug. 26, 2025
Job Description
Job Type: Remote Education: PharmD, PhD, M.Pharm, MS Pharm, MBBS, BDS, MDS 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 and Scientific Reviewer

Department: Clinical & Medical
Job Family: Medical & Regulatory Affairs
Employment Type: Full-time
Location: Remote (Work from Home)
Travel Requirement: Up to 10%
Work Hours: ~40+ hours/week


Company Overview

EVERSANA is a leading global provider of next-generation commercialization services to the life sciences industry. With over 7,000 employees worldwide and more than 650 clients—from biotech startups to global pharmaceutical leaders—our mission is to create a healthier world. Our services support drug development, regulatory, market access, medical information, and patient services, helping bring innovative therapies to market and improve patient outcomes.

We are committed to building a diverse and inclusive workplace, aligned with our Cultural Beliefs:

  • Patient Minded – Act with the patient’s best interest in mind

  • Client Delight – Own every client experience and its impact

  • Take Action – Be empowered and empower others to act now

  • Grow Talent – Own your development and support others

  • Win Together – Collaborate passionately for shared success

  • Communication Matters – Foster transparent, timely dialogue

  • Embrace Diversity – Promote awareness and respect

  • Always Innovate – Be bold and creative in everything


Position Summary

As a Medical and Scientific Reviewer, you will play a key role in EVERSANA’s Global Medical Content Development and Medical/Scientific Review Team. You will be responsible for fact-checking, reviewing, and ensuring scientific accuracy and compliance of promotional and non-promotional materials across a wide range of therapeutic areas.

This position requires strong medical/scientific expertise, attention to detail, regulatory knowledge, and the ability to interpret and communicate complex data effectively.


Key Responsibilities

Medical & Scientific Review

  • Perform scientific fact-checking and review of promotional and non-promotional materials for MLR (Medical, Legal, Regulatory) review.

  • Verify accuracy, completeness, and contextual appropriateness of all claims and content.

  • Ensure:

    • Data is scientifically balanced, clinically relevant, and statistically valid

    • References are acceptable and adequately support claims

    • Consistency with approved label and medical strategy

  • Collaborate with internal teams and client medical signatories to ensure alignment and compliance.

Content Development & Process Support

  • Support creation of materials such as:

    • Scientific Response Documents (SRDs)

    • FAQs, slide decks, posters, abstracts, and training materials

  • Review and annotate documents using tools like Veeva PromoMats / MedComms

  • Provide input to SOPs, templates, checklists, and style guides

  • Participate in client meetings and collaborate on strategic communication approaches

Project & Quality Management

  • Ensure timely resolution of issues impacting review timelines

  • Recommend improvements to reduce recurring content or process issues

  • Maintain compliance with industry standards and regulatory requirements

  • Proactively address quality issues and ensure corrective actions


Required Qualifications

Education

  • One of the following degrees:

    • PharmD, PhD, M.Pharm, MS Pharm, MBBS, BDS, MDS

Experience

  • 2+ years of experience in scientific writing or quality control in the pharmaceutical/life sciences industry

  • Experience in:

    • Scientific literature searches and analysis (PubMed, Embase, RightFind, Ovid, etc.)

    • Document review and referencing in Veeva Vault or similar platforms

    • Clinical trials, medical terminology, and the drug development lifecycle

    • Working across multiple therapeutic areas (e.g., oncology, rare diseases, immunology)

Skills & Competencies

  • Strong medical/scientific acumen

  • Excellent written and verbal communication

  • Detail-oriented with excellent time management

  • Proficiency in Microsoft Office, Adobe Acrobat, and other documentation tools

  • Ability to work independently and cross-functionally

  • Deep understanding of regulatory requirements for Medical Affairs, Medical Information, and promotional material review

  • Experience with medical content development and reference validation


Preferred Attributes

  • Strong project management and stakeholder collaboration experience

  • Ability to thrive in a fast-paced, matrix environment

  • High level of professional integrity and ethical conduct

  • Agile learner with the ability to work across multiple disease areas


Work Environment & Culture

  • Remote-first flexibility

  • Inclusive and collaborative team culture

  • Opportunities for growth and continuous learning

  • Supportive of diversity, equity, and inclusion

  • Commitment to client delight and patient-centered outcomes


Important Notes

  • EVERSANA is aware of fraudulent job offers misusing its name. We never request payment or personal information during the hiring process.

  • EVERSANA is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, gender, disability, veteran status, religion, or other protected characteristics.


Apply Now

Visit EVERSANA Careers to submit your application or follow us on LinkedIn or Twitter for updates.