Expert Writer, Medical Content Development – EVERSANA (Remote, Pune, India)
Location: Pune, Maharashtra, India (Remote Eligible)
Department: Clinical & Medical
Function: Medical Writing
Employment Type: Full-Time
Company Overview
EVERSANA is a global leader in life sciences commercialization, delivering next-generation solutions across pharmaceutical, biotechnology, medical device, and digital therapeutics sectors. With a workforce of more than 7,000 professionals and a presence across markets worldwide, the organization is committed to bringing innovative therapies to patients through integrated services and deep scientific expertise.
The company serves over 650 clients, ranging from early-stage biotechs to established global pharmaceutical companies. EVERSANA is recognized for its inclusive culture, strong ethical values, and its dedication to improving patient outcomes.
Position Overview
EVERSANA is seeking an Expert Writer, Medical Content Development to support medical affairs, medical information, scientific communications, and cross-functional content development initiatives. This role reports directly to the Manager, Medical Content Development and collaborates closely with internal teams across Medical Information, Medical Affairs, Regulatory, Pharmacovigilance, and Quality.
The position involves developing high-quality scientific content for diverse clients in pharmaceuticals, biotechnology, medical devices, digital therapeutics, and over-the-counter product sectors, including established and early-stage companies.
Experience Required
Minimum 4 years of medical writing and scientific content development experience within the life sciences or pharmaceutical industry.
Advanced degree preferred: PharmD, M.Pharm, MS Pharm, PhD, or MD.
Demonstrated experience in Medical Information, Medical Communications, or Scientific Communications.
Experience with literature review platforms (PubMed, Embase, Ovid) and reference management tools (EndNote, Mendeley, Citavi).
Strong familiarity with AMA Style Guide, ICMJE, GPP, and other medical publication guidelines.
Experience with Veeva PromoMats/MedComms preferred.
Prior experience developing content for medical information materials, scientific response documents, FAQs, slide decks, and new product launch materials is highly desirable.
Key Responsibilities
Develop scientific and medical content including Scientific Response Documents, FAQs, slide sets, abstracts, posters, training materials, and medical education content.
Lead content development for client engagements, ensuring scientific rigor, accuracy, compliance, and strategic alignment.
Support end-to-end document development including material gathering, authoring, review facilitation, and MLR (Medical, Legal, Regulatory) alignment.
Serve as content owner within document management platforms such as Veeva PromoMats or MedComms.
Perform scientific data verification and fact-checking to support medical reviewers.
Collaborate with cross-functional teams and participate in key client discussions to ensure alignment with objectives.
Contribute to thought leadership initiatives including newsletters, blogs, industry publications, and congress materials.
Support creation and refinement of SOPs, templates, style guides, and internal process documents.
Mentor junior writers and support onboarding activities as required.
Stay updated on medical writing best practices, evolving technologies, and regulatory expectations.
Deliver high-quality, accurate content within established timelines while proactively addressing quality or compliance concerns.
Work independently on multiple therapeutic areas including oncology, neurology, immunology, and rare disease domains.
Job Expectations
Ensure delivery of high-quality scientific content aligned with client expectations.
Collaborate effectively within matrix teams and adhere to regulatory, ethical, and compliance standards.
Independently interpret complex scientific data and translate it into clear, structured content.
Manage timelines, coordinate reviews, and maintain workflow efficiency.
Travel up to 10 percent, if required (post-COVID).
Average workload: 40+ hours per week.
Required Skills and Competencies
Excellent written, verbal, and presentation communication skills.
Strong understanding of clinical research methodologies and applied statistics.
Proficiency in Microsoft Office, Adobe Acrobat, and scientific research tools.
Ability to manage multiple projects simultaneously and meet strict deadlines.
High integrity, ethical decision-making, and strong attention to detail.
Ability to collaborate across business units and interact with senior stakeholders.
Agile learner with capability to work across multiple disease areas and therapeutic domains.
Preferred Qualifications
Prior experience authoring medical information materials for product launches.
Published abstracts, posters, or manuscripts.
Experience managing content within Veeva Vault MedComms or PromoMats.
Experience writing across diverse therapeutic areas.
Work Culture and Values
EVERSANA is committed to a culture built around ethics, innovation, diversity, and patient-centricity. The organization emphasizes:
Patient-focused decision making
Client satisfaction and project excellence
Transparent communication
Collaboration across teams and global functions
Continuous innovation and professional growth
Respect for diverse perspectives and backgrounds
EVERSANA also actively warns candidates about recruitment fraud. The company does not request payments or sensitive personal information during the hiring process.
Equal Opportunity Statement
EVERSANA is an Equal Opportunity Employer. The company values diversity across age, gender identity, disability, veteran status, orientation, religion, and all backgrounds.
How to Apply
Interested candidates can apply through the official EVERSANA career portal or relevant job channels. Qualified applicants are encouraged to submit their profiles even if their experience does not match every requirement.
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