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Regulatory Writer

3-5 years
Not Disclosed
10 April 22, 2025
Job Description
Job Type: Full Time Education: MBBS/MD 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

 


Regulatory Writer

Location: Mumbai or Hyderabad, India
Work Location Type: Office (On-Site)
Job ID: REQ-10048706
Date Posted: April 16, 2025
Category: Research & Development
Division: Development
Business Unit: Innovative Medicines
Company/Legal Entity: Novartis Healthcare Private Limited
Employment Type: Full-time, Regular
Shift Work: No


About the Role:

Novartis is seeking a talented and detail-oriented Regulatory Writer to join their Development team. The Regulatory Writer will be responsible for authoring, reviewing, and managing the production of high-quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. This position also provides documentation consultancy to other line functions and actively contributes to continuous improvement initiatives within Regulatory Writing Services (RWS).


Roles & Responsibilities:

  • Author and review high-quality clinical and safety documents including:

    • Non-registration Clinical Study Reports (CSRs)

    • Development Safety Update Reports (DSURs)

    • Risk Management Plans (RMPs)

  • Serve as the lead for outsourced Narrative projects and coordinate other outsourced RWS activities.

  • Act as a core member of Clinical Trial Teams (CTT) and participate in Safety Management Teams (SMT).

  • Participate in the planning of data analyses and presentations used in CSRs.

  • Provide consultancy to CTTs and SMTs to ensure documentation compliance with internal standards and external regulatory guidelines.

  • May act as a Program Writer, ensuring adequate medical writing resources and consistency across program documents.

  • Serve as a liaison between CTTs and publishing teams to ensure timely delivery of final documents.

  • Support the development of Regulatory Writing Services (RWS) through participation in workstreams and related activities.

  • Contribute to process development initiatives within RWS and cross-functional teams.

  • Foster cross-functional communication to optimize feedback for high-quality documentation.

  • Maintain compliance with audit requirements, Standard Operating Procedures (SOPs), and training standards.


Key Performance Indicators:

  • Timely delivery of high-quality clinical and safety documents.

  • Customer, partner, and project satisfaction and feedback.

  • Adherence to Novartis policies and guidelines.


Minimum Requirements:

Work Experience:

  • Minimum 3–5 years of medical writing experience, or 1–3 years with an MBBS or PhD.

  • Good knowledge of and experience with the global regulatory environment, processes, and safety reporting requirements.

  • Understanding of drug registration processes (especially for simple submissions).

Skills and Competencies:

  • Excellent written, verbal, and presentation communication skills.

  • Strong understanding of biostatistics principles.

  • Ability to prioritize and manage multiple demands and projects.

  • Strong problem-solving capabilities.

  • Broad knowledge and a future-oriented perspective.

  • Proven ability to work in a matrix environment.

  • Experience contributing to global, cross-functional projects.

  • Global, cross-cultural perspective with a strong customer orientation.


Why Novartis:

At Novartis, making a difference for patients and their families goes beyond innovative science. It involves a vibrant community of passionate people collaborating and inspiring each other to create breakthroughs that change lives. Join us in building a brighter future together.

Learn more about our people and culture here.
Explore benefits and rewards at Novartis.


Accessibility and Accommodation:

Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you need assistance during the recruitment process, please contact:
Email:
diversityandincl.india@novartis.com
Please include the job requisition number in your message.

Novartis is dedicated to creating an inclusive environment and building diverse teams representative of the patients and communities we serve.