Novartis Regulatory Writer Jobs for MBBS candidates – Apply Online!
About Novartis:
Novartis is a leading global healthcare company based in Switzerland, committed to reimagining medicine to improve and extend people’s lives. With a strong focus on innovative science and digital technologies, Novartis develops and delivers breakthrough treatments in areas such as oncology, neuroscience, cardiovascular, and immunology. Operating in over 150 countries, Novartis combines cutting-edge research with a patient-centric approach to address some of the world’s most challenging health issues.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Learn more about Novartis here.
- Job Posting: Regulatory Writer
- Job ID: REQ-10048706
- Date Posted: Apr 16, 2025
- Location: India
Summary
To write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide documentation related consultancy to other line functions.
About the Role:
Major Accountabilities:
- To author and review high quality clinical and safety documents: non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Risk Management Plans (RMP).
- Lead for outsourced Narrative projects. Coordinate other outsourced activities in RWS.
- Core member of Clinical Trial Team (CTT) / participate in Safety Management Team (SMT).
- Actively participate in planning of data analyses and presentation used in CSRs.
- Act as documentation consultant in CTTs and SMTs to ensure compliance of documentation to internal company standards and external regulatory guidelines.
- May act as Program Writer ensuring adequate medical writing resources are available for assigned program and consistency between documents.
- Act as liaison between CTTs and publishing teams to ensure timely delivery of final documents for publishing.
- Support the development of RWS through participating in RWS workstreams and other related activities.
- Contribute to development of processes within RWS. May contribute to cross-functional initiatives.
- Fostering cross-functional communication to optimize feedback and input towards high quality documents.
- Maintain audit, SOP and training compliance.
Key Performance Indicators:
- Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards
- Customer / partner/ project feedback and satisfaction
- Adherence to Novartis policy and guidelines
Minimum Requirements:
Work Experience:
- Minimum 3-5 years of medical writing experience or 1-3 years of experience with MBBS/PhD.
- Good knowledge of and some experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements).
- Knowledge of process for and some experience in global registering of drugs (simple submissions).
- Excellent communication skills (written, verbal, presentations)
- Very good understanding of biostatistics principles.
- Ability to prioritize and manage multiple demands and projects.
- Ability to define and solve complex problems (“Problemsolver”)
- Broad knowledge and future oriented perspective
- Proven track record in a matrix environment
- Experience in contributing to global, cross-functional projects
- Global, cross-cultural perspective and customer orientation
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Keywords: Novartis, regulatory writer, medical writing, clinical study reports, safety documentation, global regulatory environment, jobs
