Pharmacovigilance Advisor

Pharmacovigilance Advisor

Play a critical role in patient safety while ensuring compliance across one of our most important growth markets.

Your new role

As a Pharmacovigilance Advisor youll be instrumental in maintaining the highest safety standards for our products in China. Youll serve as a key liaison between local operations and global safety teams ensuring that every safety signal is captured assessed and acted upon in compliance with both local regulations and Novo Nordisk standards.

Your responsibilities will include:

• Supporting local PV compliance management to ensure all safety activities are processed in accordance with Chinese regulations and Novo Nordisk SOPs
• Providing safety oversight and communications on customer engagement programs (CEPs) co-promotional/co-marketing activities and digital initiatives including training qualification assessment and SDEA review
• Collecting reviewing processing and distributing customer complaints and safety information in a timely and quality manner
• Ensuring high-quality and timely submission of individual case safety reports to Global Safety and local Health Authorities according to internal SOPs and local regulations
• Preparing reviewing and submitting periodic and aggregate safety reports according to local requirements (PSUR device PRER annual reports and other safety documents)
• Monitoring local PV regulatory requirements from authorities performing gap analysis and ensuring implementation and compliance
• Providing comprehensive trainings for internal and external stakeholders including vendors and CROs and mentoring new/junior product safety staff

Your skills & qualifications

Were looking for an experienced pharmacovigilance professional who combines technical expertise with a genuine commitment to patient safety. Youll bring with you:

• Bachelors degree or above in clinical medicine pharmacy or relevant field
• Minimum 6 years experience in pharmaceutical industry or related industry such as medical devices or healthcare
• Minimum 5 years specifically in pharmacovigilance function
• Strong familiarity with China EU and ICH pharmacovigilance legislation
• Proven ability to manage safety information in compliance with Good Documentation Practice (GDP) and regulatory requirements
• Excellent communication and training skills with ability to engage diverse stakeholders including vendors health authorities and internal teams
• Strong organizational skills and attention to detail in managing complex compliance requirements

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this we approach our work with determination constant curiosity and a commitment to finding better ways forward. For over 100 years this dedication has driven us to build a company focused on lasting change for long-term pharmacovigilance this means never compromising on patient safety while continuously improving our processes and systems. Youll work in a culture where diverse thinking shared purpose and mutual respect come together to create extraordinary results. When you join us youre not just starting a job youre becoming part of a story that spans generations.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk were not chasing quick fixes were creating lasting change for long-term health. For over 100 years weve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of whats possible in healthcare. We embrace diverse perspectives seek out bold ideas and build partnerships rooted in shared purpose. Together were making healthcare more accessible treating and preventing diseases and pioneering solutions that create change spanning generations. When you join us you become part of something bigger a legacy of impact that reaches far beyond today.