EVERSANA hiring Medical Content Reviewer Role | Pharm D, M Pharm Candidates Apply
Looking for a pharma job in Medical Affairs and Scientific Content Review? EVERSANA is hiring qualified life sciences professionals to join its global medical content development and review team. This opportunity is ideal for candidates seeking an EVERSANA career in medical communications, scientific review, medical affairs, and pharmaceutical content development.
- Job Title: Medical and Scientific Reviewer
- Location: Chinchwad
About the Company
EVERSANA is a global life sciences services organization with over 7,000 employees dedicated to improving patient outcomes worldwide. The company provides end-to-end commercialization services to pharmaceutical, biotechnology, medical device, and healthcare companies. Through innovation, scientific expertise, and patient-focused solutions, EVERSANA supports more than 650 clients across multiple therapeutic areas.
Job Description
EVERSANA is seeking experienced professionals to support medical content development, scientific review, and medical affairs activities. This pharma job involves reviewing promotional and non-promotional materials, ensuring scientific accuracy, supporting Medical, Legal, and Regulatory (MLR) reviews, and contributing to high-quality medical communications across various therapeutic areas.
Key Responsibilities
- Review and fact-check scientific, promotional, and non-promotional materials.
- Ensure medical accuracy, regulatory compliance, and scientific balance.
- Evaluate claims, references, and supporting clinical data.
- Support Medical, Legal, and Regulatory (MLR) review processes.
- Review medical content against approved product labels and regulations.
- Collaborate with medical affairs, scientific reviewers, and client teams.
- Support development of FAQs, slide decks, training materials, abstracts, and scientific documents.
- Conduct literature searches and scientific data analysis.
- Manage content using platforms such as Veeva PromoMats and MedComms.
- Participate in client meetings and content strategy discussions.
- Contribute to SOPs, templates, guidance documents, and quality improvement initiatives.
Qualifications & Experience
- Education: Pharm D, M Pharm, M.S. Pharm, Ph.D.
- Experience:
- Minimum 2 years of experience in scientific writing, scientific review, document QC, or medical communications within the pharmaceutical or life sciences industry.
- Experience in Medical Affairs, Medical Information, or Medical Communications preferred.
Required Skills
- Scientific data analysis and literature review.
- Knowledge of clinical trials and drug development.
- Proficiency in PubMed, Embase, Ovid, RightFind, and Veeva platforms.
- Scientific writing and content review.
- Strong communication, presentation, and project management skills.
- Excellent attention to detail and stakeholder coordination.
Preferred Experience
- Medical Affairs, Medical Information, or Scientific Communications.
- Promotional and non-promotional content review.
- Experience across therapeutic areas such as Oncology, Immunology, Hematology, and Rare Diseases.
- Understanding of US pharmaceutical regulations and promotional review requirements.
Additional Information
- Travel Requirement: Up to 10%
- Work Schedule: Average 40+ hours per week
- Global collaboration with cross-functional medical and scientific teams
- Opportunity to work with leading pharmaceutical and biotechnology companies
- Diverse and inclusive work environment
