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Expert Writer, Medical Content Development

Eversana
EVERSANA
4+ years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 (Remote – Pune, India)

Company: EVERSANA
Location: Pune, Maharashtra, India (Remote)
Job Type: Full-Time
Department: Clinical & Medical
Job Family: Medical Writing
Experience Required: 4+ years in Medical Writing / Medical Information / Scientific Communications


Position Overview

EVERSANA is seeking an Expert Writer for Medical Content Development to deliver high-quality, scientifically accurate medical and scientific content for global clients in the pharmaceutical, biotechnology, medical device, digital therapeutics, and over-the-counter sectors. This role supports clients ranging from emerging biotech companies to established pharmaceutical organizations and contributes to integrated commercialization, Medical Information (MI), and Medical Affairs (MA) engagements.

The successful candidate will collaborate with cross-functional teams, including Medical Affairs, Medical Information, Pharmacovigilance, Regulatory, and Quality, to develop impactful medical content in alignment with regulatory and industry standards.


Key Responsibilities

Medical Content Development

  • Create and review medical and scientific content including:

    • Scientific Response Documents (SRDs)

    • FAQs, slide decks, abstracts, posters

    • Education and training materials

  • Drive the content development process from research and drafting to Medical/Legal/Regulatory (MLR) review facilitation

  • Ensure scientific accuracy, clarity, and compliance of all content

  • Manage content on document management systems (e.g., Veeva PromoMats / MedComms)

Client & Project Support

  • Collaborate with Manager, Medical Content Development on strategic content projects

  • Participate in client meetings and contribute to project planning, execution, and feedback

  • Support thought leadership initiatives including publications, congress materials, newsletters, and blogs

  • Mentor and coach junior team members; assist with onboarding and team development

Regulatory & Compliance

  • Maintain awareness of regulatory requirements and best practices in Medical Information, Medical Affairs, and medical communications

  • Ensure compliance with industry standards and internal SOPs

  • Flag and manage quality issues and implement corrective actions

Collaboration & Cross-Functional Work

  • Work with EVERSANA teams across MI, MA, Pharmacovigilance, Regulatory, and Quality functions

  • Support multiple therapeutic areas, disease states, and client types in a flexible, agile environment

Travel & Work Schedule

  • Up to 10% business travel (post-COVID)

  • Full-time, approximately 40+ hours/week, with flexibility as required


Required Qualifications

Education:

  • Pharm.D., M.Pharm, M.S. Pharm, PhD, or MD with relevant medical writing/content development experience

Experience & Skills:

  • Minimum 4 years in life sciences or pharmaceutical industry with strong medical writing and content development background

  • Direct experience in Medical Information, Medical Communications, or Scientific Communications

  • Strong understanding of clinical research principles, applied statistics, and medical publishing guidelines (ICMJE, GPP, CONSORT, PRISMA, STROBE)

  • Familiarity with AMA Style Guide and scientific literature evaluation

  • Proficient in Microsoft Office, Acrobat, and reference management tools (EndNote, Mendeley, Citavi)

  • Excellent written, oral, and presentation skills; ability to interpret and summarize complex scientific data

  • Strong project management skills with a results-driven mindset

  • High ethical standards and professionalism

Preferred Qualifications:

  • Experience in medical content development for new product launches

  • Experience publishing abstracts, posters, or manuscripts

  • Multi-therapeutic area experience

  • Experience with Veeva Vault MedComms / PromoMats


Why Join EVERSANA

  • Remote work flexibility in Pune, India

  • Opportunity to develop high-impact medical content across multiple therapeutic areas

  • Work with a global, inclusive, and innovative life sciences organization

  • Contribute to projects that enhance patient care and scientific communication


Cultural Beliefs

  • Patient Minded: Act in the patient’s best interest

  • Client Delight: Take ownership of client experiences

  • Take Action: Empower yourself and others to act now

  • Grow Talent: Invest in your development and that of others

  • Win Together: Collaborate passionately to achieve results

  • Communication Matters: Maintain transparent, thoughtful dialogue

  • Embrace Diversity: Foster awareness and respect

  • Always Innovate: Be bold and creative in everything you do


Apply Now

EVERSANA is looking for an Expert Medical Content Writer to create, review, and manage high-quality scientific content for clients worldwide. Join a collaborative, cross-functional team and make an impact on patient care and the global life sciences industry.