Are you passionate about making a difference in the healthcare industry? Novartis, a global leader in pharmaceuticals, is hiring for the role of Global Clinical Publishing Associate (Job ID: REQ-10042152). This is an exciting opportunity to contribute to groundbreaking projects that improve patient lives worldwide. Read on to learn more about the job responsibilities, requirements, and how to apply.
Job Overview: Global Clinical Publishing Associate
Location: India
Job ID: REQ-10056544
Posting Date: August 27, 2025 (30+ days left to apply)
Novartis is seeking a Global Clinical Publishing Associate to manage regulatory documentation, ensure compliance with global standards, and support the development and maintenance of life-saving products. If you have a background in clinical study reports, data analysis, and regulatory compliance, this role is perfect for you.
Key Responsibilities
As a Global Clinical Publishing Associate, you will:
- Manage medium to small-scale global regulatory submission projects.
- Ensure compliance with regulatory requirements for documentation and record retention.
- Provide technical and strategic input for global product development and maintenance.
- Collaborate with internal and external stakeholders to drive project success.
- Report technical complaints, adverse events, and special case scenarios within 24 hours.
This role requires a strong understanding of lifesciences, operational excellence, and documentation management.
🎓 What Degrees Are Eligible?
Novartis has not specified exact degrees, but based on the required skills and typical industry standards, the following degrees are commonly eligible:
✅ Eligible Degrees (with 3–5 years of relevant experience):
- B.Pharm / M.Pharm
- M.Sc. in Life Sciences (Biotechnology, Biochemistry, Microbiology, etc.)
- Pharm.D
- B.Sc. + Experience in Regulatory Affairs or Publishing
- B.E. / B.Tech (Life Science or IT related) – with training in regulatory affairs
Skills
To excel in this role, you should have:
- Experience in cross-cultural collaboration and project management.
- Strong skills in data analysis and regulatory compliance.
- Knowledge of clinical study reports and documentation management.
- Excellent communication skills in English.
Work Experience:
- Functional breadth in operations management and execution.
- Proven ability to collaborate across boundaries.
Why Join Novartis?
At Novartis, we believe in empowering our employees to make a difference. Here’s why you should join us:
- Be part of a community that values collaboration and innovation.
- Work on projects that transform patient lives globally.
- Access to competitive benefits and rewards.
- Opportunities for professional growth and development.
The Global Clinical Publishing Associate role sits at the intersection of both Regulatory Affairs and Clinical Research, but it is more closely aligned with Regulatory Affairs.
| Category | Is it Core to the Role? | Notes |
|---|---|---|
| Regulatory Affairs | ✅ Yes (Primary) | Core responsibility is submission publishing. |
| Clinical Research | ✅ Yes, but secondary | You support clinical teams, but don’t conduct trials or data analysis. |
