Novartis has announced an exciting opportunity for Clinical Scientific Expert I at its Hyderabad office. This role is ideal for professionals interested in clinical research, clinical trial management, clinical data review, patient safety, and global drug development. As a core member of the Clinical Trial Team (CTT), you will contribute to the successful execution of global clinical trials while ensuring compliance with ICH-GCP, regulatory guidelines, and Novartis quality standards.
If you are looking to build your career in Clinical Research Jobs in India, Novartis Clinical Trial Jobs, or Clinical Scientific Expert Jobs in Hyderabad, this opportunity offers exposure to global studies, cross-functional collaboration, and scientific excellence.
Job Details
| Particular | Details |
|---|---|
| Company | Novartis |
| Position | Clinical Scientific Expert I |
| Department | Clinical Development |
| Job Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Application Deadline | July 30, 2026 |
| Experience | Relevant Clinical Research Experience |
| Qualification | Bachelor’s or Master’s Degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or related field |
| Industry | Pharmaceutical / Clinical Research |
About the Role
The Clinical Scientific Expert I (CSE I) supports global clinical studies throughout the clinical development lifecycle. Working under the guidance of senior clinical development leaders, the role focuses on clinical data review, protocol support, patient safety evaluation, scientific insights, and cross-functional trial execution.
The successful candidate will ensure high-quality clinical trial delivery while maintaining compliance with ICH-GCP, regulatory requirements, and Novartis operating procedures.
Key Responsibilities
- Support execution of global clinical trials from study initiation to completion.
- Perform comprehensive clinical data review and identify scientific insights.
- Evaluate clinical data trends, patient safety signals, and endpoint consistency.
- Contribute to protocol development, informed consent forms (ICF), and clinical sections of Clinical Trial Applications (CTA).
- Collaborate with Clinical Development, Data Management, Drug Supply Management, and Country Organizations.
- Participate in issue resolution planning and study risk mitigation.
- Maintain inspection-ready documentation throughout study execution.
- Report adverse events, technical complaints, and special case scenarios within required timelines.
- Support program-level clinical development activities as assigned.
- Ensure compliance with ICH-GCP, regulatory requirements, and Novartis quality standards.
Required Qualifications
Candidates with the following educational backgrounds are encouraged to apply:
- B.Pharm
- M.Pharm
- Pharm.D
- MBBS
- MD
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Biomedical Sciences
- Biological Sciences
- Other relevant Life Sciences disciplines
Required Skills
- Clinical Research
- Clinical Trial Management
- Clinical Trial Protocol Development
- Clinical Data Review
- Clinical Data Integrity
- Patient Safety
- Risk Monitoring
- Trend Analysis
- Cross-functional Collaboration
- Project Management
- ICH-GCP Compliance
- Regulatory Compliance
- English Communication
Preferred Experience
Candidates having exposure to:
- Clinical Development
- Global Clinical Trials
- Clinical Data Review
- Risk-based Monitoring
- Clinical Operations
- Cross-cultural Collaboration
- Scientific Documentation
will be preferred.
Why Join Novartis?
Working at Novartis provides opportunities to:
- Contribute to innovative global clinical development programs.
- Work with international clinical trial teams.
- Gain exposure to advanced clinical data review methodologies.
- Build expertise in patient safety and scientific evaluation.
- Learn from experienced clinical development leaders.
- Grow within one of the world’s leading pharmaceutical organizations.
- Access continuous professional development and global career opportunities.
How to Apply
