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Medical And Scientific Reviewer

2 years years
not specified
10 Sept. 5, 2025
Job Description
Job Type: Remote Education: PharmD, PhD, MBBS, BDS, MDS, or M.Pharm / M.S. Pharm 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
Location: Remote (U.S.-based)
Employment Type: Full-Time
Department: Clinical & Medical
Job Family: Medical & Regulatory Affairs


Company Overview

EVERSANA is a global leader in next-generation commercialization services for the life sciences industry. With over 7,000 employees serving 650+ clients — from start-ups to global pharmaceutical leaders — we support the full product life cycle and the patients who depend on these therapies.

We are Great Place to Work® certified and committed to building a diverse and inclusive team that prioritizes client delight, patient outcomes, and innovation in everything we do.


Position Summary

As a Medical and Scientific Reviewer, you will be part of EVERSANA’s global medical content development and review team, supporting clients across a wide range of therapeutic areas including oncology, rare diseases, neurology, immunology, cardiology, dermatology, infectious diseases, and more.

You will ensure medical and scientific accuracy, compliance, and clarity in both promotional and non-promotional materials, supporting internal teams and clients through MLR (Medical, Legal, Regulatory) review processes.


Key Responsibilities

Content Review & Medical Accuracy

  • Review promotional and non-promotional materials for scientific accuracy, clinical/statistical relevance, and regulatory compliance.

  • Ensure all claims are:

    • Fair and balanced

    • Adequately supported by evidence

    • Aligned with approved product labeling

  • Determine acceptability of references and advise on data relevance.

  • Collaborate with internal/client medical reviewers and material sponsors to resolve findings.

Cross-Functional Collaboration

  • Participate in MLR review meetings and provide scientific input.

  • Partner with internal stakeholders (Medical Affairs, Medical Information, Medical Writers) and client teams.

  • Use tools like Veeva PromoMats / MedComms to annotate, upload, and manage documents.

Content Development Support

  • Assist in developing scientific materials such as:

    • Scientific Response Documents (SRDs)

    • FAQs

    • Slide decks

    • Abstracts & Posters

    • Training and education resources

  • Ensure alignment with client strategies and regulatory standards.

  • Support documentation processes, SOPs, templates, and style guides.

Operational Excellence

  • Proactively identify and resolve quality issues or process inefficiencies.

  • Meet or exceed deadlines and ensure materials meet internal and external quality standards.

  • Participate in continuous improvement initiatives for content review processes.


Qualifications

Required Education & Experience

  • PharmD, PhD, MBBS, BDS, MDS, or M.Pharm / M.S. Pharm

  • Minimum 2 years of experience in scientific/medical writing or document quality control in life sciences or pharmaceutical industries

Skills & Competencies

  • Deep scientific/medical knowledge across multiple therapeutic areas (e.g., oncology, rare diseases, immunology)

  • Proficient in literature search platforms (e.g., PubMed, Ovid, Embase, RightFind)

  • Understanding of:

    • Medical terminology

    • Clinical trials and drug development

    • Regulatory requirements and best practices for Medical Affairs/Information

  • Strong analytical and critical thinking skills

  • Excellent verbal and written communication skills

  • Ability to interpret complex data and tailor it for different audiences (e.g., HCPs, patients, payers)

  • Experienced with content review platforms (e.g., Veeva Vault PromoMats / MedComms)

  • Highly organized with strong project management and time management abilities

  • Proficient with Microsoft Office, Adobe Acrobat, and other productivity tools


Work Environment & Expectations

  • Work Hours: Average of 40+ hours/week

  • Travel: Up to 10% (as required)

  • Teamwork: Collaborate across EVERSANA’s internal business units and with client teams

  • Independence: Capable of reviewing and delivering high-quality, compliant medical content independently


Preferred Attributes

  • Proven track record in multiple therapeutic areas

  • Experience participating in MLR review processes

  • Strong ethical standards and attention to detail

  • Adaptability and quick learning in new therapeutic areas

  • Proactive in process improvement and quality management


Our Cultural Beliefs

  • Patient Minded – Act in the best interest of patients

  • Client Delight – Own every client experience and outcome

  • Take Action – Empower yourself and others to move forward

  • Grow Talent – Invest in your development and others’ growth

  • Win Together – Collaborate openly to achieve shared success

  • Communication Matters – Prioritize transparent, thoughtful dialogue

  • Embrace Diversity – Foster inclusion and respect for all perspectives

  • Always Innovate – Think creatively and boldly


Equal Opportunity Employer

EVERSANA is an Equal Opportunity Employer committed to a diverse and inclusive workplace. We value all backgrounds, identities, and experiences and believe diversity strengthens our teams and helps us deliver better results for clients and patients.


Recruitment Fraud Alert

Please be aware of fraudulent job offers claiming to be from EVERSANA. We never request payment or sensitive personal information during our hiring process. Visit our official website to verify open positions and job communications.


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