Company: EVERSANA
Location: Pune / Remote
Industry Type: Pharma / Healthcare / Clinical Research
Last Date to Apply: 25th June 2025
About EVERSANA
EVERSANA is a leading global provider of services to the life sciences industry, offering integrated solutions that enhance patient experiences and support pharmaceutical products throughout their lifecycle. With a commitment to innovation and compliance, EVERSANA serves over 670 organizations, including top pharmaceutical companies and emerging biotech firms, ensuring safe and effective healthcare solutions worldwide.
Current Job Openings at EVERSANA
EVERSANA is hiring qualified professionals in Medical Information, Medical Review, and Medical Content Development for candidates with backgrounds in:
- B.Pharm / M.Pharm
- Pharm.D
- MSc Lifesciences
- MBBS / BDS / MDS
- Ph.D. in Biomedical Sciences
1. Medical Information Specialist
Job Description:
- Respond to medical inquiries from healthcare professionals, patients, and payers.
- Research and evaluate medical literature to prepare accurate responses.
- Handle adverse event (AE) and product quality complaint reporting.
- Ensure compliance with FDA regulations and client-specific requirements.
Qualifications:
- Education: B.Pharm / M.Pharm / Pharm.D / MSc Lifesciences
- Skills: Strong clinical knowledge, excellent communication, and documentation skills.
- Experience: Prior experience in medical information or pharmacovigilance preferred.
2. Medical and Scientific Reviewer
Job Description:
- Review promotional and non-promotional materials for scientific accuracy.
- Ensure compliance with medical, legal, and regulatory (MLR) guidelines.
- Collaborate with cross-functional teams for content approval.
- Fact-check data and verify references for medical claims.
Qualifications:
- Education: Pharm.D / M.Pharm / Ph.D. / MBBS / MDS
- Experience: 2+ years in medical writing, scientific review, or MLR processes.
- Skills: Strong analytical skills, knowledge of Veeva Vault PromoMats/MedComms.
3. Medical Content and Review Specialist
Job Description:
- Manage end-to-end MLR review processes.
- Schedule and document review committee meetings.
- Support medical content development and FDA submissions.
- Ensure compliance with industry regulations.
Qualifications:
- Education: Life Sciences / Biomedical graduates
- Experience: 2+ years in healthcare agencies or pharma companies.
- Skills: Project management, Veeva Vault proficiency, scientific writing.
Medical Information Specialist Link
Medical Content and Review Specialist Link