Expert Medical Content Writer – Life Sciences
Location: Pune, Maharashtra, India (Remote Option Available) | Employment Type: Full-Time | Department: Clinical & Medical | Job Family: Medical Writing
Company Overview
EVERSANA® is a global leader in life sciences commercialization, delivering next-generation solutions that bring innovative therapies to market and support patients worldwide. With a diverse team of over 7,000 professionals, we serve more than 650 clients, including emerging biotech startups, established pharmaceutical companies, and medical device organizations. At EVERSANA, we are committed to creating an inclusive culture, fostering professional growth, and delivering measurable impact to patients and clients alike.
We are recognized as a Great Place to Work®, reflecting our dedication to employee development, collaboration, and ethical excellence in everything we do.
Job Overview
EVERSANA is seeking an Expert Medical Content Writer to join our Compliance and Medical Content Development team. Reporting to the Manager, Medical Content Development, this role focuses on delivering high-quality, scientifically accurate, and compliant medical content for pharmaceutical, biotechnology, medical device, and digital therapeutics clients. The position requires experience in medical writing, medical information, and medical affairs across multiple therapeutic areas, including Oncology, Neurology, Immunology, and Immuno-oncology.
This role is ideal for professionals with strong scientific communication skills, regulatory knowledge, and a proven ability to create impactful content for global life sciences clients.
Key Responsibilities
Develop, review, and finalize scientific and medical content, including:
Scientific Response Documents (SRD), FAQs, slide sets, abstracts, posters, training materials, and other client-facing medical communications.
Lead content development projects from initial research to final review, ensuring scientific rigor, compliance, and alignment with client objectives.
Collaborate with cross-functional teams including Medical Affairs, Pharmacovigilance, Regulatory, and Quality to ensure content accuracy and compliance.
Utilize content management platforms such as Veeva PromoMats/MedComms to manage, upload, and annotate documents.
Conduct literature reviews, fact-check data, and synthesize complex scientific information into clear, concise messaging.
Mentor and support junior medical writers; contribute to hiring, onboarding, and training initiatives.
Participate in client meetings, providing strategic input and subject matter expertise.
Assist in developing SOPs, templates, style guides, and process improvements to enhance content quality and operational efficiency.
Maintain awareness of industry trends, best practices, and evolving compliance standards.
Required Qualifications
Education: PharmD, M. Pharm, M.S. Pharm, PhD, or MD with relevant medical writing experience.
Experience: Minimum of 4 years in medical writing, medical communications, or medical information within the pharmaceutical, biotech, or life sciences industry.
Strong knowledge of clinical research principles, applied statistics, and therapeutic areas relevant to client portfolios.
Familiarity with AMA Style Guide, ICMJE, GPP, CONSORT, PRISMA, STROBE, and other medical publishing guidelines.
Exceptional written, oral, and interpersonal communication skills.
Proficiency in Microsoft Office Suite, Acrobat, literature databases (PubMed, Embase, Ovid), and reference management tools (EndNote, Mendeley, Citavi).
Proven project management skills, with the ability to manage multiple tasks and meet deadlines in a dynamic environment.
High ethical standards, integrity, and professionalism.
Ability to collaborate across business units and with client stakeholders globally.
Willingness to travel up to 10% post-COVID restrictions.
Preferred Qualifications
Experience developing content for new product launches and medical information materials.
Track record of publishing abstracts, posters, manuscripts, or congress presentations.
Experience across multiple therapeutic areas.
Familiarity with Veeva Vault MedComms/PromoMats or similar content management platforms.
Why Join EVERSANA
Contribute to innovative therapies that improve patient lives globally.
Engage with diverse, cross-functional teams in a collaborative environment.
Access structured mentoring, professional development, and career growth opportunities.
Competitive benefits package, flexible work arrangements, and a culture that values inclusion, integrity, and innovation.
Cultural Beliefs at EVERSANA:
Patient Minded: Always prioritize patient outcomes.
Client Delight: Deliver exceptional client experiences.
Take Action: Proactively drive results and empower others.
Grow Talent: Invest in personal growth and development of colleagues.
Win Together: Collaborate to achieve shared goals.
Communication Matters: Encourage transparent and thoughtful dialogue.
Embrace Diversity: Foster an inclusive and respectful environment.
Always Innovate: Apply creativity and bold thinking in every project.
How to Apply
Join EVERSANA and be part of a global team shaping the future of medical content development and life sciences innovation. Apply today and make a tangible impact on patients, clients, and the healthcare industry.
Equal Opportunity Employer: EVERSANA celebrates diversity and inclusion and encourages applicants from all backgrounds to apply.
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