Expert Scientific Writer
Novartis
Expert Scientific Writer
Job Description
Summary
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.Locations
- India
Salary
Estimated Salary Rangemedium confidence
70,000 - 120,000 INR / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical documentation writingintermediate
- Safety documentation managementintermediate
- Regulatory submission expertiseintermediate
- Documentation reviewintermediate
- Consultancy provisionintermediate
- Quality assurance in documentationintermediate
- Marketing application supportintermediate
Required Qualifications
- Experience in clinical and safety documentation (experience)
Responsibilities
- Write high quality clinical documentation
- Review clinical and safety documentation
- Manage production of documentation for regulatory submission
- Support marketing applications to regulatory authorities
- Provide documentation consultancy to line functions
Answer 10 quick questions to check your fit for Expert Scientific Writer @ Novartis.
10 Questions
~2 Minutes
Instant Score
Expert Scientific Writer
Novartis
Expert Scientific Writer
Job Description
Summary
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.Locations
- India
Salary
Estimated Salary Rangemedium confidence
70,000 - 120,000 INR / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical documentation writingintermediate
- Safety documentation managementintermediate
- Regulatory submission expertiseintermediate
- Documentation reviewintermediate
- Consultancy provisionintermediate
- Quality assurance in documentationintermediate
- Marketing application supportintermediate
Required Qualifications
- Experience in clinical and safety documentation (experience)
Responsibilities
- Write high quality clinical documentation
- Review clinical and safety documentation
- Manage production of documentation for regulatory submission
- Support marketing applications to regulatory authorities
- Provide documentation consultancy to line functions
Answer 10 quick questions to check your fit for Expert Scientific Writer @ Novartis.
10 Questions
~2 Minutes
Instant Score