Medical and Scientific Reviewer
Location: Pune, Maharashtra, India (Remote Work Available)
Employment Type: Full-time
Department: Clinical & Medical
Job Family: Medical & Regulatory Affairs
Company: EVERSANA
Job Overview
EVERSANA is seeking a highly skilled Medical and Scientific Reviewer to join its global medical content development and scientific review team. This role focuses on ensuring scientific accuracy, regulatory compliance, and quality assurance of promotional and non-promotional medical materials across multiple therapeutic areas. The position requires strong expertise in scientific literature evaluation, medical communications, and regulatory standards within the pharmaceutical and life sciences industry.
The successful candidate will contribute to global medical affairs initiatives by reviewing scientific content, supporting medical communications, and ensuring alignment with regulatory guidelines, clinical data, and approved product labeling. This is an excellent opportunity for professionals looking to advance their careers in medical affairs, medical information, and scientific communications within a globally recognized healthcare organization.
About the Organization
EVERSANA is a global provider of commercialization services to the life sciences industry, supporting pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to market. With a workforce of more than 7,000 professionals worldwide, the organization delivers integrated solutions in medical affairs, regulatory support, and patient-focused healthcare services. The company partners with over 650 clients, ranging from emerging biotech firms to established pharmaceutical leaders, with a strong commitment to improving patient outcomes globally.
Key Responsibilities
Conduct scientific data verification and review promotional and non-promotional materials for medical, legal, and regulatory (MLR) review processes.
Ensure medical content is scientifically accurate, clinically relevant, balanced, and compliant with regulatory standards.
Validate claims, references, and clinical data for accuracy and consistency with approved product labeling.
Review and proofread medical materials for editorial and scientific accuracy.
Analyze and interpret scientific literature and clinical data across therapeutic areas.
Collaborate with medical reviewers, medical writers, and cross-functional teams to ensure timely review and approval of materials.
Support development of medical affairs content including scientific response documents, slide decks, FAQs, training materials, and educational content.
Ensure alignment of content with client medical strategies and industry regulations.
Identify quality issues, propose process improvements, and support corrective actions.
Manage documentation using content management and review platforms such as Veeva Vault PromoMats or MedComms.
Participate in client meetings and support strategic medical communications initiatives.
Assist in developing SOPs, templates, style guides, and compliance documentation.
Work independently to deliver high-quality, compliant, and scientifically rigorous content.
Therapeutic Area Exposure
The role supports multiple therapeutic areas including oncology, hematology, rare diseases, immunology, cardiology, dermatology, neurology, infectious diseases, respiratory, endocrinology, women’s health, and related specialties.
Experience Required
Minimum 2 years of experience in scientific writing, document quality control, or medical content review within the pharmaceutical or life sciences industry.
Experience in reviewing promotional and non-promotional medical materials is preferred.
Experience in medical affairs, medical information, or scientific communications is advantageous.
Prior exposure to multiple therapeutic areas and regulatory review processes is desirable.
Educational Qualifications
PharmD, M.Pharm, MS Pharm, PhD, MBBS, BDS, or MDS with relevant experience in scientific writing or reviewing.
Required Skills and Competencies
Strong knowledge of medical terminology, clinical research, and drug development processes.
Expertise in literature search and analysis using databases such as PubMed, Ovid, Embase, or similar tools.
Understanding of regulatory standards governing pharmaceutical promotional and non-promotional materials.
Ability to analyze complex scientific data and communicate findings to healthcare professionals and other stakeholders.
Strong attention to detail and excellent editorial skills.
Experience with content development and document management platforms such as Veeva Vault.
Effective communication, presentation, and stakeholder management skills.
Strong project management and time management capabilities.
Ability to work in cross-functional, matrix-based global teams.
Work Environment and Expectations
Remote working flexibility available.
Travel requirements up to 10%.
Standard work schedule averaging 40+ hours per week.
Diversity, Equity, and Inclusion
EVERSANA is an equal opportunity employer committed to fostering a diverse and inclusive workplace. The organization values diverse perspectives and promotes innovation, collaboration, and professional growth while working toward improving patient outcomes worldwide.
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