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Expert Writer, Medical Content Development

Eversana
EVERSANA
4+ years
Not Disclosed
Pune, India
10 March 19, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Expert Writer – Medical Content Development | Medical Writing & Medical Affairs

Location: Pune, Maharashtra, India (Remote/Hybrid)
Company: EVERSANA
Job Type: Full-Time
Department: Clinical & Medical | Medical Writing

Job Overview
EVERSANA is seeking an experienced Expert Writer – Medical Content Development to join its global Medical Writing and Compliance team. This role is responsible for developing high-quality, scientifically accurate, and regulatory-compliant medical content across a wide range of therapeutic areas including oncology, neurology, immunology, and rare diseases.

The position plays a key role in supporting Medical Affairs, Medical Information, and Medical Communications initiatives, working closely with cross-functional teams to deliver impactful content aligned with client strategies and global compliance standards.

Key Responsibilities

Medical Content Development

  • Develop and author high-quality medical and scientific content including:

    • Scientific Response Documents (SRDs)

    • Frequently Asked Questions (FAQs)

    • Slide decks, abstracts, posters, and manuscripts

    • Training and educational materials

  • Ensure content is scientifically rigorous, accurate, and aligned with client medical strategies

Client & Project Management

  • Lead end-to-end document development from data gathering to final delivery

  • Support Medical, Legal, and Regulatory (MLR) review processes

  • Collaborate with internal stakeholders and clients to ensure timely project execution

  • Participate in client meetings and provide strategic content input

Scientific Review & Data Interpretation

  • Analyze and interpret complex clinical and scientific data

  • Conduct literature searches using tools such as PubMed, Embase, and Ovid

  • Perform scientific fact-checking and ensure proper referencing and citation

Compliance & Quality Assurance

  • Ensure all content complies with global regulatory standards and industry guidelines

  • Follow best practices including ICMJE, GPP, CONSORT, PRISMA, and STROBE guidelines

  • Maintain high standards of editorial quality, consistency, and accuracy

Cross-Functional Collaboration

  • Work closely with Medical Affairs, Medical Information, Pharmacovigilance, Regulatory, and Quality teams

  • Collaborate with creative teams and other medical writers to deliver integrated solutions

  • Mentor junior team members and support onboarding and training initiatives

Process Improvement & Innovation

  • Contribute to development of SOPs, templates, and style guides

  • Support thought leadership content such as publications, blogs, and newsletters

  • Stay updated on industry trends, tools, and technologies to enhance content quality and efficiency

Required Qualifications

  • PharmD, M.Pharm, MS Pharm, PhD, or MD in Life Sciences or related field

  • Strong understanding of clinical research, medical communications, and regulatory requirements

  • Familiarity with medical writing guidelines and publication standards

Experience Required

  • Minimum 4+ years of experience in medical writing, medical content development, or scientific communications within the pharmaceutical or life sciences industry

  • Proven experience in Medical Information, Medical Affairs, or Medical Communications

  • Experience handling MLR review processes and working with content management platforms such as Veeva Vault

Preferred Experience

  • Experience supporting new product launches and medical information content

  • Publication experience (abstracts, posters, manuscripts)

  • Exposure to multiple therapeutic areas

Key Skills

  • Medical Writing & Scientific Content Development

  • Clinical Data Analysis & Interpretation

  • Regulatory Compliance & MLR Review

  • Literature Search & Evidence Synthesis

  • Project Management & Client Handling

  • Attention to Detail & Quality Control

  • Communication & Stakeholder Engagement

Why Join EVERSANA?

  • Be part of a global leader in life sciences commercialization services

  • Work on innovative therapies across diverse therapeutic areas

  • Collaborative and inclusive work culture with global exposure

  • Strong focus on professional growth, learning, and leadership development

About EVERSANA
EVERSANA is a leading global provider of integrated commercialization services to the life sciences industry, supporting over 650 clients worldwide. With a workforce of 7,000+ professionals, the company delivers end-to-end solutions that help bring innovative therapies to market and improve patient outcomes globally.

How to Apply
Interested candidates can apply through EVERSANA’s official careers portal or submit their updated resume on ThePharmaDaily.com to explore similar opportunities in Medical Writing, Medical Affairs, and Scientific Communications.