Medical Job Opportunity: Senior GCP Advisor at Novo Nordisk Bangalore
Looking for a high-impact medical job in clinical quality and compliance? Novo Nordisk is hiring a Senior GCP Advisor in Bangalore, Karnataka. This opportunity is ideal for experienced professionals in Good Clinical Practice (GCP), quality management systems, and clinical trials who are passionate about ensuring global compliance and excellence in drug development. If you are exploring Novo Nordisk careers, GCP jobs, or medical jobs in Bangalore, this role could be your next big career move.
Job Details:
- Job Position: Senior GCP Advisor
- Company: Novo Nordisk
- Department: Novo Nordisk Quality GBS – R&D Quality
- Location: Bangalore, Karnataka, India
- Application Deadline: 1 March 2026
About the Company:
Novo Nordisk is a global healthcare company headquartered in Denmark with more than 100 years of innovation in defeating diabetes and other serious chronic conditions. The company develops and manufactures innovative biological medicines to benefit people living with diabetes, obesity, rare blood disorders, and endocrine diseases. Through continuous research and development, Novo Nordisk transforms unmet medical needs into life-saving and preventive medicines. If you are exploring Novo Nordisk careers, this organization offers a strong global presence, an innovative research culture, and a meaningful impact on patients’ lives.
Job Description:
This medical job focuses on managing Content Control and Process Management processes for clinical trials while ensuring compliance with Good Clinical Practice (GCP) regulations on behalf of Process Quality Assurance (PQA). As a Senior GCP Advisor, you will:
- Serve as a GCP Advisor and member of the Clinical Trial (CT) SOP Council
- Advise the line of business regarding quality concerns and ensure a quality mindset
- Provide support during GCP inspections
- Drive continuous quality improvement initiatives
- Ensure global consistency and compliance in clinical development processes
Qualifications:
To qualify for this senior-level medical job, candidates must have:
- Degree in medical or similar
- Minimum 10–12 years of experience within GCP and clinical trial conduct
- Strong knowledge of the pharmaceutical business and GCP regulations in drug development
- Extensive experience conducting clinical trials
- Experience in QMS and quality processes
- Audit and inspection support experience
- In-depth understanding of drug development and lifecycle management
- Project management and global coordination skills
- Ability to present complex quality issues effectively
Key Responsibilities:
- Verify and approve Standard Operating Procedures (SOPs) and ensure correct interpretation of GCP regulations as a quality advisor
- Collaborate with Novo Nordisk Process Managers following Process Management guidelines
- Communicate regularly with Process Quality Assurance Delegate (PQAD)
- Maintain global CT SOPs and ensure compliance with internal and external requirements
- Attend CT SOP council meetings and raise, present, and discuss quality concerns
- Work independently using strong GCP knowledge and stay updated with changing regulations and QMS needs
- Support stakeholders during GCP inspections
- Ensure global consistency in clinical development through documentation, guidance, and information sharing
- Act as a quality anchor for worldwide clinical development processes
