Safety Surveillance Adviser Novo Nordisk – MBBS/MD Candidates Apply Now!
Category: Regulatory Affairs & Safety Pharmacovigilance
Location: Bangalore, Karnataka, IN
Department: Global Safety – Global Business Services (GS-GBS)
Do you thrive in a dynamic work environment where collaboration and strategic alignment are key? Are you passionate about safety surveillance and regulatory compliance? If so, this position at Novo Nordisk could be the perfect opportunity for you. Join us and be part of a global leader in healthcare.
The Position
As a Safety Surveillance Adviser, you will play a crucial role in establishing and maintaining the product safety profile during development and post-marketing phases. Your key responsibilities include:
- Conducting systematic safety surveillance of Novo Nordisk (NN) products.
- Communicating drug safety issues to internal teams and health authorities (HAs).
- Leading the cross-functional safety committee to review ongoing safety data.
- Managing safety-related aspects of clinical trials and regulatory documentation.
- Preparing safety-related sections of DSURs, SUSAR reports, PSURs, and RMPs.
- Providing safety input to product development plans, clinical trial protocols, and investigator brochures.
- Responding to inquiries from health authorities and ethics committees.
Qualifications
- Master’s in Medicine (MD) or MBBS preferred.
- Experience in Signal Management, Aggregate Management, and ICSR.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Strong analytical and organizational skills with a quality-focused mindset.
- Excellent communication skills in English.
- Adaptable, proactive, and a team player with cross-cultural awareness.
About the Department
Global Safety – Global Business Services (GS-GBS) was established in 2010 as a hub for safety case processing. The team manages case processing from various sources, including spontaneous, literature, solicited, and clinical trials. Key activities include medical review, safety report submission, ICSR quality control, signal detection, risk mitigation, and literature surveillance.
Working at Novo Nordisk
Novo Nordisk is a global healthcare leader with a 100-year legacy in fighting chronic diseases. With over 63,000 employees worldwide, we are committed to driving change, impacting millions of lives, and fostering an inclusive and diverse work culture. Join us and make a difference.
Application Process
Deadline: 28 March 2025
How to Apply: Upload your CV and motivational letter online by clicking “Apply.” Internal candidates should inform their line managers before applying.
Important Notice
Novo Nordisk does not charge any fees during the recruitment process. Be cautious of fraudulent job offers that ask for personal information or payments.
At Novo Nordisk, we aspire to be the best company in the world by fostering a culture of inclusion and diversity. Join us on this mission—Together, we’re life-changing.
Keywords: Pharmacovigilance, Drug Safety, Clinical Trials, Risk Management, Regulatory Affairs. Safety Surveillance Adviser Novo Nordisk
