Location: Pune, Maharashtra, India (Remote / Hybrid Available)
Company: EVERSANA
Job Type: Full-Time
Department: Clinical & Medical | Medical & Regulatory Affairs
Experience Required: Freshers or Minimum 2+ years (Freshers are eligible)
About the Company
EVERSANA is a globally recognized life sciences services organization focused on delivering next-generation commercialization solutions. With a workforce of 7,000+ professionals and a client base of over 650 organizations—including biotech startups and leading pharmaceutical companies—EVERSANA plays a critical role in bringing innovative therapies to market and improving patient outcomes worldwide.
Job Overview
The Medical and Scientific Reviewer is a key role within global medical content development and Medical Affairs teams. This position requires strong scientific expertise, regulatory understanding, and precision in reviewing promotional and non-promotional materials. The role involves working across multiple therapeutic areas and ensuring that all medical communications meet compliance, accuracy, and quality standards aligned with global regulatory expectations.
Key Responsibilities
Perform scientific review and fact-checking of promotional and non-promotional materials for Medical, Legal, and Regulatory (MLR) submissions
Ensure medical content is scientifically accurate, clinically relevant, and compliant with regulatory standards
Validate claims against scientific literature and approved product labeling
Review references for credibility, adequacy, and alignment with claims
Ensure balanced and non-misleading presentation of scientific data
Collaborate with medical signatories, medical writers, and cross-functional teams to ensure timely approval of materials
Identify risks, inconsistencies, and quality issues impacting timelines and compliance
Support development of Medical Affairs content including Scientific Response Documents (SRDs), FAQs, slide decks, abstracts, posters, and training materials
Participate in MLR review meetings and provide scientific insights
Utilize platforms such as Veeva Vault PromoMats / MedComms for content management and approval workflows
Contribute to SOP development, templates, and process improvement initiatives
Work across multiple therapeutic areas including oncology, immunology, rare diseases, cardiology, and more
Ensure adherence to global regulatory standards, industry codes, and compliance frameworks
Required Qualifications
Educational Background: PharmD, M.Pharm, M.S. Pharm, PhD, MBBS, BDS, or MDS
Minimum 2+ years of experience in scientific writing, medical review, or document QC in the pharmaceutical or life sciences industry
Strong understanding of clinical trials, drug development lifecycle, and medical terminology
Experience in literature search and analysis using databases such as PubMed, Embase, Ovid, or RightFind
Knowledge of MLR review process and regulatory requirements for promotional and non-promotional materials
Hands-on experience with Veeva Vault PromoMats or MedComms preferred
Excellent analytical, writing, editing, and communication skills
Strong attention to detail and ability to manage multiple projects under strict timelines
Preferred Skills and Competencies
Experience in Medical Affairs, Medical Information, or Scientific Communications
Ability to interpret complex clinical data and translate it for diverse audiences including healthcare professionals and patients
Cross-functional collaboration skills in a matrix environment
Strong project management and problem-solving abilities
Adaptability to work across diverse therapeutic areas
Work Environment and Expectations
Flexible remote or hybrid work model
Standard working hours with potential extension based on project requirements
Up to 10% travel, depending on business needs
Why This Role Matters
This position sits at the intersection of science, compliance, and communication. It offers exposure to global pharmaceutical clients, diverse therapeutic areas, and high-impact medical content that directly supports patient care and regulatory decision-making.
Important Note for Applicants
This is a mid-level role requiring prior experience in medical review, scientific writing, or Medical Affairs. Freshers are advised to begin with entry-level roles such as Drug Safety Associate, Medical Writer, or Clinical Research roles before progressing to MLR review positions.
How to Apply
Apply through the official careers page of EVERSANA or explore verified global pharma opportunities on ThePharmaDaily.com.
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