Job Title: Senior Scientific Writer
Location: Hyderabad, India
Company: Novartis Healthcare Private Limited
Employment Type: Full-Time
Experience Required: 4–8+ years in Clinical Research/Medical Writing
Novartis is a global healthcare leader dedicated to reimagining medicine to improve and extend people’s lives. With a mission to become the most valued and trusted medicines company worldwide, Novartis fosters a culture of innovation, collaboration, and inclusion, driving breakthrough therapies that transform patient outcomes.
The Senior Scientific Writer will be responsible for creating high-quality scientific content, including publications, presentations, and core medical content, aligned with strategic scientific narratives. This role ensures accuracy, compliance, and first-time-right delivery across all deliverables, supporting clinical research, regulatory requirements, and marketing activities.
Develop scientific and medical documents such as abstracts, posters, slide decks, manuscripts (including subgroup analyses and real-world evidence studies), and congress materials.
Support medical education materials and omni-channel communications aligned with therapeutic area priorities.
Perform quality control (QC) checks and proofreading to ensure compliance with internal and external standards.
Manage multiple projects simultaneously, maintaining timelines and delivering high-quality outputs.
Gather and implement feedback from internal stakeholders to enhance document quality and relevance.
Maintain accurate project documentation, archives, and audit readiness in line with SOPs and regulatory standards.
Comply with Novartis specifications for documentation, templates, and processes.
Education:
B.Sc. or equivalent + 8 years of Clinical Research experience, or
M.Sc./M.Pharm + 6 years of Clinical Research experience, or
PhD + 4 years of Clinical Research experience, or
MBBS/MD or equivalent + 2–4 years of Clinical Research experience
Skills & Expertise:
Strong knowledge of scientific writing, clinical research, and regulatory requirements.
Experience preparing medical and scientific documents for publication, regulatory submissions, and marketing support.
Proficiency in adhering to publication standards such as CONSORT and journal formatting requirements.
Ability to manage multiple projects efficiently while maintaining quality and deadlines.
Excellent communication skills for cross-functional collaboration and interaction with internal and external stakeholders.
Proven ability to build strong relationships with clients, KOLs, and internal teams.
Experience in designing and improving processes to meet compliance and quality standards.
Strong attention to detail and a commitment to delivering first-time-right scientific content.
Be part of a global innovation-driven organization dedicated to improving patient outcomes.
Work in an inclusive and collaborative environment that values diversity and professional growth.
Access comprehensive benefits and rewards to support personal and professional development.
Contribute to scientific communication that shapes healthcare decisions globally.
Apply Now to join Novartis as a Senior Scientific Writer and help drive impactful medical communications across therapeutic areas.
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
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Paris | Lyon |South Africa :
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