Chemistry & Pharma Jobs, Senior Regulatory Writer Post @ Novartis

Chemistry & Pharma Jobs, Senior Regulatory Writer Post @ Novartis

Pharmaceutical Science Senior Regulatory Writer. Applications are invited for the post of Senior Regulatory Writer @ Novartis.Career @ Novartis. Pharma job opportunity at Novartis. Senior Regulatory Writer post vacancy. Interested candidates may apply online. Check out all the details on the same below:

Job Id: 268826BR

Job Title: Senior Regulatory Writer

Eligibility: Masters Degree in Science or Pharmacy

Experience: Minimum 6 years to 10 years of relevant experience in medical writing


  • Advanced knowledge of and experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements).
  •  Advanced knowledge of and repeat experience in global registration of drugs (complex submissions).
  •  Ability to plan and priorities workload
  •  Ability to work in a matrix environment
  •  Ability to build effective relationships across teams
  • Active command in English with excellent written and spoken communication skills
  • Adequate knowledge of software and computer tools.
  • Creative thinking and effective interdisciplinary collaboration with other functions.

Job Description

Your responsibilities:

Your responsibilities include, but are not limited to: 

1. To the author, review and manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Risk Management Plans (RMP), submission

documents (e.g., summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics).

2.A core member of Clinical Trial Team (CTT) / contributor to Safety Management Team.

3.A major contributor to planning of data analyses and presentation used in CSRs and submission documents.

4.Documentation specialist in CTTs and Clinical Submission Teams (CST) to ensure compliance of documentation to internal company standards and external regulatory guidelines. Provide content expertise and guidance for clinical portions of the CTD.

5. Program Writer ensuring adequate medical writing resources are available for assigned program and consistency between documents. Extended member of International Clinical Team (ICT)

6. Lead Writer for simple submissions, contributing to key messaging and pooling strategy, providing content guidance, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. Core member of CST.

7. Contribute to process improvement in RWS and/or cross-functional initiatives or activities.

Apply Online

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