Novartis is a global healthcare leader focused on reimagining medicine to improve and extend lives. With a strong commitment to innovation, diversity, and inclusion, Novartis offers a dynamic work environment where employees drive meaningful impact in patient care.
📍 Location: Hyderabad (Hybrid)
📅 Last Date to Apply: July 30, 2025
📌 Job ID: REQ-10057727
Job Description
Key Responsibilities:
- Prepare high-quality medical and scientific communications, including literature reviews, abstracts, posters, slide sets, and complex manuscripts.
- Perform quality control (QC) checks to ensure accuracy and compliance.
- Manage multiple projects across two brands simultaneously.
- Follow Novartis documentation standards (Novstyle, templates, etc.).
- Track clinical trial milestones and maintain project records.
- Ensure compliance with SOPs, audits, and training requirements.
- Train new team members as needed.
Skills Required:
✔ Clinical Research
✔ Medical Writing
✔ Regulatory Compliance
✔ Detail-Oriented
✔ Clinical Trials
Eligibility Criteria
Minimum Requirements:
- B.Sc. + 8 years of Clinical Research (CR) experience
- M.Sc./M.Pharm + 6 years of CR experience
Preferred Qualifications:
- PhD + 4 years of CR experience
- MBBS/MD + 2 – 4 years of CR experience
- Strong background in scientific/medical writing
Why Join Novartis?
✅ Impactful Work: Contribute to life-changing medical innovations.
✅ Career Growth: Opportunities for professional development.
✅ Hybrid Work Model: Flexible office & remote work options.
✅ Inclusive Culture: Diverse and collaborative work environment.
📌 Employee Benefits:
- Competitive salary & bonuses
- Health & wellness programs
- Learning & development opportunities
