Medical and Scientific Reviewer

Why This Role Matters
The Medical and Scientific Reviewer ensures that all promotional and non-promotional materials, scientific documents, and medical communications are accurate, scientifically balanced, and compliant with applicable regulations. By reviewing content across multiple therapeutic areas, interpreting scientific literature, and supporting medical affairs and information teams, this role helps clients deliver high-quality, ethical, and scientifically rigorous information to healthcare professionals and patients. The position ensures both regulatory compliance and medical accuracy, contributing directly to patient safety and informed decision-making.

Job Description
The Medical and Scientific Reviewer is responsible for reviewing, fact-checking, and approving scientific and medical content for promotional and non-promotional materials. The role involves analyzing literature, preparing scientifically rigorous documents, supporting medical affairs, and ensuring alignment with medical strategies. The reviewer collaborates with internal teams, clients, and medical signatories, maintaining compliance with regulatory requirements and best practices. This position also contributes to SOP creation, process improvements, and content management using platforms like Veeva Vault PromoMats / MedComms.

Key Features Of The Role
• Review and fact-check promotional and non-promotional materials for medical, legal, and regulatory compliance
• Ensure scientific accuracy, clinical and statistical relevance, and balanced presentation of data
• Evaluate claims, references, and alignment with approved product labels
• Support medical content creation including SRDs, FAQs, slide decks, abstracts, posters, and training materials
• Collaborate with internal and client medical signatory reviewers for timely document approval
• Use content management tools (e.g., Veeva Vault PromoMats / MedComms) for document upload, referencing, and annotations
• Identify, communicate, and resolve issues impacting timelines or content quality
• Propose content and process improvements to reduce recurring errors
• Participate in client meetings and contribute to strategic discussions on medical communications
• Support SOP, template, checklist, and style guide creation and updates

Responsibilities
• Conduct thorough scientific review of medical and promotional content across multiple therapeutic areas
• Analyze and interpret scientific literature, clinical trials, and regulatory data
• Ensure all content is scientifically accurate, contextually correct, and aligned with medical strategy
• Review claims for accuracy, relevance, and adequate supporting data
• Collaborate with medical, regulatory, and creative teams to resolve findings and approve content
• Support medical affairs and medical information teams with content creation and document development
• Ensure compliance with US regulations, industry codes of practice, and internal standards
• Manage multiple projects and meet deadlines while maintaining high-quality outputs
• Flag quality issues proactively and implement corrective or preventive actions
• Support cross-functional collaboration across EVERSANA business units and client teams

Required Qualifications

Educational Requirements
• PharmD, M.Pharm, MS Pharm, Ph.D., BDS, MDS, or MBBS with relevant experience in scientific writing or reviewing

Experience And Skills
• Minimum of 2 years of experience in scientific writing, document QC, or medical content review within life sciences or pharmaceuticals
• Experience across multiple therapeutic areas including oncology, immunology, rare diseases, and others
• Proficient in literature searches and analysis using PubMed, Ovid, Embase, RightFind, etc.
• Strong medical and scientific knowledge, with understanding of clinical trials, drug development, and medical terminology
• Experience with content management platforms (e.g., Veeva Vault PromoMats / MedComms)
• Excellent communication, editing, and project management skills
• High attention to detail, analytical thinking, and ability to translate complex data for different audiences
• Knowledge of US regulations and best practices for medical communications and promotional materials
• Ability to work independently and collaboratively in a matrix team environment

Salary Insights
• Compensation as per company norms and industry standards
• Opportunities to work remotely and exposure to global medical communications projects
• Career growth in medical affairs, regulatory, and scientific communications

Company Overview
EVERSANA is a global life sciences services provider, supporting more than 650 clients with commercialization, medical, regulatory, and scientific services. The company emphasizes diversity, inclusion, and professional development while delivering high-quality medical content to improve patient outcomes. EVERSANA values integrity, collaboration, and scientific excellence across all therapeutic areas.

FAQs
Q: What type of materials will I review?
A: Promotional and non-promotional materials, scientific responses, FAQs, slide sets, abstracts, posters, and medical training materials.

Q: Will I interact with clients?
A: Yes, the role involves collaboration with internal teams, medical signatory reviewers, and client representatives.

Q: What tools are used for content management?
A: Veeva Vault PromoMats, MedComms, Microsoft Office, Acrobat, and other content management platforms.

Application Tips
• Highlight experience in medical or scientific content review across therapeutic areas
• Emphasize familiarity with regulatory requirements and industry best practices
• Showcase expertise in literature analysis, scientific writing, and document QC
• Demonstrate project management, attention to detail, and collaborative skills