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Medical And Scientific Reviewer

EVERSANA
2+ years
8-15 LPA
Pune, Pune city, India
10 June 10, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical and Scientific Reviewer | 2–5 Years Experience | Salary: 8–15 LPA


Job Description

EVERSANA is hiring a Medical and Scientific Reviewer to join its Clinical & Medical team in Pune. This is a remote-friendly role focused on reviewing and validating scientific, medical, promotional, and non-promotional content for pharmaceutical, biotechnology, and healthcare clients. The position plays a critical role in ensuring medical accuracy, scientific integrity, regulatory compliance, and strategic alignment of content used across multiple therapeutic areas.

The ideal candidate will possess strong scientific knowledge, experience in medical review or scientific writing, and the ability to interpret complex clinical data and literature while collaborating with cross-functional teams.


Key Responsibilities

Scientific Review & Medical Content Validation

  • Perform scientific fact-checking and review of promotional and non-promotional materials submitted for Medical, Legal, and Regulatory (MLR) review.

  • Ensure scientific accuracy, clinical relevance, completeness, and balanced presentation of data.

  • Verify that claims are appropriately supported by scientific evidence and references.

  • Assess the acceptability and quality of scientific references.

  • Ensure content aligns with approved product labeling and medical strategy.

  • Review and proofread medical content for accuracy, consistency, and compliance.

Medical Affairs & Regulatory Support

  • Collaborate with medical signatories and reviewers to ensure efficient and compliant content approval.

  • Support review discussions and resolve medical review findings with content owners and stakeholders.

  • Identify and escalate issues impacting quality or project timelines.

  • Contribute recommendations for process improvements and content optimization.

  • Support adherence to industry regulations and pharmaceutical compliance standards.

Medical Content Development Support

  • Assist in creating and reviewing scientific response documents (SRDs), FAQs, slide decks, abstracts, posters, educational materials, and training content.

  • Support Medical Affairs, Medical Information, and Medical Communications projects.

  • Facilitate document review processes and MLR review meetings.

  • Support development and maintenance of SOPs, templates, style guides, and review checklists.

Cross-Functional Collaboration

  • Work closely with medical writers, scientific reviewers, creative teams, and client stakeholders.

  • Participate in client meetings and strategic discussions when required.

  • Support multiple therapeutic areas and client projects simultaneously.

  • Ensure timely delivery of high-quality scientific content and reviews.


Required Qualifications

  • PharmD, M.Pharm, M.S. Pharm, PhD, MBBS, BDS, or MDS.

  • Minimum 2 years of experience in scientific writing, scientific review, medical communications, or document quality control within the pharmaceutical or life sciences industry.

  • Experience reviewing promotional and non-promotional medical content.


Required Skills

  • Strong scientific and medical knowledge across therapeutic areas such as Oncology, Hematology, Immunology, Rare Diseases, and related specialties.

  • Ability to critically analyze and interpret scientific literature and clinical data.

  • Experience with literature databases such as PubMed, Ovid, Embase, and RightFind.

  • Knowledge of clinical trial design, drug development, and medical terminology.

  • Understanding of pharmaceutical regulations governing promotional and non-promotional materials.

  • Experience with Veeva Vault PromoMats and/or Veeva Vault MedComms.

  • Excellent medical writing, editing, proofreading, and communication skills.

  • Strong project management and time management capabilities.

  • High attention to detail and commitment to quality.

  • Ability to work independently and manage multiple projects simultaneously.

  • Proficiency in Microsoft Office Suite and document management platforms.

  • Strong collaboration and stakeholder management skills.