- Full Time
- Pune / Remote

Website EVERSANA
Table of Contents
ToggleAbout EVERSANA
EVERSANA is a leading global provider of integrated services to the life sciences industry. From market access and pricing to patient services and compliance, our end-to-end solutions are rooted in the patient experience and span the product lifecycle. Serving over 670 clients, we drive long-term, sustainable value for patients, providers, and payers alike.
Walk-In / Remote Opportunities – Apply Now for the Following Roles:
1. Medical Information Specialist
Location: Pune / Remote
Email to Apply: [careers@eversana.com]
Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc. (Life Sciences)
Experience: 0–3 years (Freshers with excellent communication skills may apply)
Key Responsibilities:
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Respond to inquiries from healthcare professionals and patients with accurate, evidence-based information
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Handle multi-channel queries via phone, email, CRM, and chat
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Identify and document adverse events and product complaints in compliance with regulatory requirements
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Conduct literature searches and write custom medical responses
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Maintain client-specific therapeutic and product knowledge
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Deliver excellent customer service with scientific accuracy
2. Medical and Scientific Reviewer
Location: Pune / Remote
Email to Apply: [careers@eversana.com]
Qualification: Pharm.D, M.Pharm, Ph.D., MBBS, MDS, BDS
Experience: Minimum 2 years in scientific writing, content QC, or medical review
Key Responsibilities:
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Review promotional and non-promotional content for scientific accuracy and compliance
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Ensure all claims are well-supported by clinical data and appropriate references
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Participate in MLR (Medical, Legal, Regulatory) review processes
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Provide quality assurance for documents using platforms like Veeva Vault
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Collaborate with cross-functional medical, content, and regulatory teams
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Support development of FAQs, scientific response documents, slide decks, and more
3. Medical Content and Review Specialist
Location: Pune / Remote
Email to Apply: [careers@eversana.com]
Qualification: Life Sciences / Biomedical graduate (B.Pharm, M.Pharm, MSc, MBBS, etc.)
Experience: Minimum 2 years in pharma agency or life sciences industry
Key Responsibilities:
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Manage end-to-end MLR review processes
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Schedule, facilitate, and document review committee meetings
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Upload and annotate documents in Veeva Vault (PromoMats/MedComms)
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Perform QC on final approved materials for FDA submission
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Collaborate with Medical Affairs for project execution and document tracking
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Ensure compliance with internal and regulatory guidelines
Why EVERSANA?
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Work with global pharma and biotech leaders
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Exposure to multiple therapeutic areas including Oncology, Neurology, Cardiology, and Rare Diseases
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Flexible remote work opportunities
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Commitment to training, professional growth, and inclusion
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Opportunity to work at the intersection of science, compliance, and patient care
Application Deadline:
Apply by: 25th June 2025
For all roles, strong English communication skills and familiarity with regulatory and medical standards are essential. Candidates with experience in Veeva Vault, medical content development, and compliance review will be given preference.
Ready to make a difference in the life sciences world?
Send your resume to careers@eversana.com with your preferred role in the subject line.
EVERSANA is an equal opportunity employer committed to diversity and inclusion in the workplace.
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