Medical and Scientific Reviewer
Organization: EVERSANA
Location: Pune, India (Remote Work Available)
Job Type: Full-Time
Department: Clinical and Medical
Job Function: Medical and Regulatory Affairs / Medical Affairs / Scientific Review
About the Organization
EVERSANA is a global provider of integrated commercialization services for the life sciences industry, supporting pharmaceutical, biotechnology, and medical device organizations in bringing innovative therapies to market. The organization delivers end-to-end medical information, medical affairs, and regulatory services across multiple therapeutic areas including oncology, immunology, cardiology, rare diseases, neurology, and infectious diseases. With a global workforce and strong commitment to improving patient outcomes, EVERSANA focuses on scientific excellence, regulatory compliance, and innovation in healthcare solutions.
Job Overview
The Medical and Scientific Reviewer will be responsible for reviewing and validating scientific and medical content for accuracy, regulatory compliance, and strategic alignment. The role involves reviewing promotional and non-promotional materials, verifying clinical claims, analyzing scientific literature, and ensuring medical content meets regulatory and industry standards.
The selected candidate will work within global medical content development and medical affairs teams, supporting medical communications, regulatory review processes, and cross-functional collaboration across multiple therapeutic areas.
Key Responsibilities
Conduct scientific review and fact-checking of promotional and non-promotional medical materials submitted for medical, legal, and regulatory review.
Ensure scientific accuracy, clinical relevance, and statistical validity of claims and data.
Verify that content aligns with approved product labels and regulatory requirements.
Evaluate references and supporting evidence for medical claims.
Review medical content for accuracy, consistency, and compliance with industry standards.
Collaborate with medical reviewers, content owners, and cross-functional teams to resolve review findings.
Support development and review of medical affairs and medical communications materials, including scientific response documents, FAQs, slide decks, abstracts, and training content.
Analyze and interpret scientific literature and clinical data for different audiences such as healthcare professionals and patients.
Support document development processes and participate in medical review meetings.
Provide recommendations for content and process improvements to enhance quality and compliance.
Work with document management platforms and content review systems to manage medical materials.
Contribute to development of standard operating procedures, templates, and quality frameworks.
Support strategic discussions and project execution within medical affairs and scientific communications teams.
Educational Qualifications
PharmD, M.Pharm, MS Pharm, PhD, MBBS, BDS, MDS, or equivalent degree in life sciences or healthcare discipline.
Experience Required
Minimum 2 years of experience in scientific writing, medical review, or document quality control within the pharmaceutical or life sciences industry.
Experience reviewing promotional and non-promotional materials in medical affairs or regulatory environments is preferred.
Experience working across multiple therapeutic areas and medical communication projects is desirable.
Required Skills and Competencies
Strong scientific and medical knowledge with ability to interpret complex clinical data.
Understanding of medical terminology, clinical trials, and drug development processes.
Experience conducting literature searches using databases such as PubMed, Embase, or similar platforms.
Knowledge of global regulatory requirements for medical affairs and promotional material review.
Strong analytical, critical thinking, and problem-solving skills.
Excellent written and verbal communication abilities.
High attention to detail and strong quality control capabilities.
Proficiency in content management and document review platforms.
Strong project management and organizational skills.
Ability to work collaboratively in cross-functional and matrix environments.
Work Environment and Expectations
Remote work flexibility with global collaboration opportunities.
Up to 10% travel may be required.
Standard full-time work schedule (approximately 40 hours per week).
Opportunity to work across multiple therapeutic areas and global medical communications projects.
Career Growth and Impact
This role offers the opportunity to contribute to global medical content development, regulatory compliance, and scientific communication initiatives that support healthcare innovation and improve patient outcomes worldwide.
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