Job Title:
Medical Writing Specialist
Company:
Novo Nordisk
Location:
Bangalore, India
About Novo Nordisk:
The Clinical Reporting unit at Novo Nordisk’s Global Business Service has seen tremendous growth since its inception in 2011. Our team comprises skilled Medical Writers, Disclosure Medical Writers, Publishers, and Document Controllers with advanced degrees in life sciences, pharmacology, and medicine. With expertise in various therapeutic areas and regulatory requirements, we ensure clear and impactful communication on clinical trials.
Position Details:
Position | Medical Writing Specialist |
---|---|
Organization | Novo Nordisk |
Qualifications | B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences |
Experience | ≥10 years |
Salary | ₹17.6 Lakhs per year |
Location | Bangalore |
Key Responsibilities:
- Communicate clinical data clearly and concisely.
- Plan, develop, and oversee regulatory documents for clinical development phases.
- Act as Project Medical Writer (PMW) and Clinical Submission Team Lead (CST).
- Mentor and train other medical writers.
- Ensure timely, clear, and proactive communication with stakeholders.
- Support the execution of Clinical Reporting strategy and vision.
- Maintain accuracy and compliance with regulatory standards.
- Drive process improvements and knowledge sharing.
- Challenge expert contributors to enhance document quality.
Qualifications:
- Graduate degree (PhD, MSc, M.Pharm, or equivalent).
- ≥10 years of experience in medical writing or relevant roles.
- Expertise in regulatory medical writing (CSRs, protocols, IBs, etc.).
- Strong understanding of clinical development and regulatory processes.
- Experience in global pharmaceutical/CRO settings.
- Excellent analytical, communication, and presentation skills.
- Proven track record of delivering high-quality work on time.
- Ability to handle multiple tasks simultaneously and improve methods.