Medical and Scientific Reviewer | Medical Affairs & Medical Communications
Location: Pune, Maharashtra, India (Remote/Hybrid)
Company: EVERSANA
Job Type: Full-Time
Department: Clinical & Medical | Medical & Regulatory Affairs
Job Overview
EVERSANA is seeking a detail-oriented Medical and Scientific Reviewer to join its global Medical Affairs and Medical Communications team. This role is critical in ensuring the scientific accuracy, regulatory compliance, and quality of promotional and non-promotional materials across multiple therapeutic areas. The position involves reviewing complex scientific data, supporting medical content development, and collaborating with cross-functional teams to deliver high-quality, compliant healthcare communications.
Key Responsibilities
Medical & Scientific Review
Conduct scientific review and fact-checking of promotional and non-promotional materials for Medical, Legal, and Regulatory (MLR) review
Ensure all content is scientifically accurate, balanced, and aligned with approved product labels
Validate claims, references, and data for clinical and statistical relevance
Ensure materials meet regulatory requirements, industry standards, and best practices
Content Quality & Compliance
Review and proofread medical content against source references for accuracy and consistency
Ensure content aligns with client medical strategies and target audience needs
Identify and resolve quality issues, ensuring timely corrective actions
Medical Content Development Support
Support development of scientific content including:
Scientific Response Documents (SRDs)
FAQs, slide decks, abstracts, and posters
Training and educational materials
Assist in preparing documents for MLR review meetings
Cross-Functional Collaboration
Work closely with medical writers, reviewers, and client stakeholders
Collaborate with medical signatories and MLR teams to ensure efficient review cycles
Participate in client meetings and provide scientific input as required
Data Analysis & Literature Review
Conduct literature searches using databases such as PubMed, Embase, and Ovid
Analyze and interpret complex scientific and clinical data
Translate scientific findings into clear, audience-appropriate communication
Process Improvement & Systems Management
Use content management systems such as Veeva Vault PromoMats/MedComms
Support development of SOPs, templates, and quality checklists
Recommend process improvements to enhance efficiency and reduce errors
Compliance & Documentation
Ensure adherence to global regulatory guidelines and compliance standards
Maintain proper documentation and audit readiness
Manage timelines and deliverables across multiple projects
Required Qualifications
PharmD, M.Pharm, MS Pharm, PhD, MBBS, BDS/MDS, or equivalent Life Sciences qualification
Strong understanding of clinical research, medical terminology, and drug development processes
Knowledge of global regulatory frameworks governing promotional and non-promotional materials
Experience Required
Minimum 2+ years of experience in scientific writing, medical review, or document quality control within the pharmaceutical or life sciences industry
Experience in Medical Affairs, Medical Information, or Medical Communications preferred
Hands-on experience with MLR review processes and content management platforms (e.g., Veeva Vault)
Key Skills
Scientific & Medical Content Review
Medical Writing & Editing
Clinical Data Interpretation
Regulatory Compliance & MLR Review
Literature Search & Evidence Analysis
Attention to Detail & Quality Assurance
Cross-Functional Collaboration
Project & Time Management
Why Join EVERSANA?
Work with a globally recognized life sciences services organization
Exposure to diverse therapeutic areas including oncology, immunology, rare diseases, and more
Collaborative and inclusive work culture focused on innovation and patient outcomes
Opportunities for career growth in Medical Affairs and Scientific Communications
About EVERSANA
EVERSANA is a leading global provider of commercialization services to the life sciences industry, supporting over 650 clients worldwide. With a team of 7,000+ professionals, EVERSANA delivers integrated solutions across the product lifecycle, helping bring innovative therapies to market and improve patient lives globally.
How to Apply
Interested candidates can apply through EVERSANA’s official careers portal or submit their updated resume on ThePharmaDaily.com to explore similar opportunities in Medical Affairs, Medical Writing, and Scientific Review.
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