EVERSANA Hiring Medical & Scientific Reviewer | Medical Affairs Role | Apply Now
Looking for a Scientific Reviewer Job in the pharmaceutical and life sciences industry? EVERSANA is hiring a Medical and Scientific Reviewer to join its global Medical Affairs and Medical Information team. This opportunity is ideal for M Pharm, PharmD, MBBS, BDS, MDS, and PhD professionals with experience in scientific writing, medical content review, and regulatory compliance. Candidates seeking an EVERSANA Career can gain exposure to Medical Affairs, Medical Communications, MLR review processes, scientific content development, and multiple therapeutic areas.
- Job Title: Medical and Scientific Reviewer
- Job Location: Pune / Pimpri-Chinchwad, Maharashtra
About the Company
An EVERSANA Career offers professionals the opportunity to work with a leading global provider of commercialization, Medical Affairs, and Medical Information services for the pharmaceutical and biotechnology industry. With a workforce of more than 7,000 professionals and support for over 650 life sciences clients worldwide, EVERSANA helps bring innovative therapies to patients through scientific, regulatory, and commercial excellence. The company partners with pharmaceutical, biotechnology, medical device, and healthcare organizations across multiple therapeutic areas, making it an attractive destination for professionals seeking a Scientific Reviewer Job and long-term growth in Medical Affairs and Scientific Communications.
Job Description
EVERSANA is hiring for a Scientific Reviewer Job within its global Medical Affairs and Medical Communications team. This Medical and Scientific Reviewer role involves reviewing promotional and non-promotional pharmaceutical materials to ensure scientific accuracy, medical relevance, and regulatory compliance. The selected candidate will collaborate with Medical, Legal, and Regulatory (MLR) teams to evaluate scientific claims, validate references, and support the development of high-quality medical content. As part of this EVERSANA Career opportunity, professionals will work across diverse therapeutic areas including oncology, immunology, rare diseases, cardiology, neurology, hematology, and respiratory medicine while contributing to Medical Affairs, Medical Information, and Scientific Communications initiatives for global life sciences clients.
Key Responsibilities
- Conduct scientific fact-checking and review of promotional and non-promotional materials.
- Ensure medical and scientific accuracy of content submitted for MLR review.
- Verify that claims are adequately supported by scientific evidence and references.
- Assess clinical and statistical relevance of medical data and claims.
- Review materials for compliance with approved product labeling and regulatory requirements.
- Proofread and validate medical content against supporting references.
- Collaborate with medical signatories and cross-functional MLR teams.
- Support development of scientific response documents, FAQs, slide decks, abstracts, posters, and training materials.
- Conduct literature evaluation and interpretation of scientific publications.
- Work with Veeva Vault PromoMats and MedComms platforms for document management and review workflows.
- Assist in developing SOPs, style guides, templates, and quality review processes.
- Participate in client discussions and provide scientific review recommendations.
- Identify quality issues and support corrective and preventive actions.
- Contribute to process improvements for medical content development and review.
Eligibility Criteria
- Education: PharmD, M Pharm
- Experience: Minimum 2 years of experience in scientific writing, document QC, scientific review, or related pharmaceutical industry functions.
Required Skills
- Scientific Writing & Medical Review
- Medical Affairs & Medical Information
- Medical Communications
- Literature Search (PubMed, Embase, Ovid, RightFind)
- Clinical Trial & Scientific Data Analysis
- MLR Review & Regulatory Compliance
- Veeva Vault PromoMats / MedComms
- Medical Content Development
- Project Management
- Quality Control & Documentation
Why Join EVERSANA?
An EVERSANA Career offers the opportunity to work at the intersection of science, medicine, and regulatory excellence. Employees gain exposure to global pharmaceutical brands, diverse therapeutic areas, and advanced Medical Affairs projects while collaborating with experienced scientific and healthcare professionals. The role provides valuable experience in medical content development, scientific communications, regulatory review, and cross-functional collaboration within the life sciences industry.
