Clinical Research Associate

Are you motivated by driving innovation for the life-changing benefit of patients Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can make it happen.

The position

• The CRA is the primary point of contact between site staff and Novo Nordisk. In this role the CRA acts as ambassador for the company and contributes to making Novo Nordisk the preferred partner.
• The CRA is responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, Novo Nordisk procedures and protocol requirements to ensure data quality and study subject protection.
• The CRA is responsible for managing the site to meet patient recruitment rate and target.
• The CRA thereby delivers results that have direct impact on the successful completion of the clinical programme.
• The CRA coordinates with LTM and RTM and communicates to them progress and critical issues that may impair trial progress.

Qualifications

• Bachelor's degree or above of Medical Science, e.g. medical, pharmacy, nursing, etc.
• Adequate English verbal and written skills
• Requires a minimum of one year clinical trial experience within pharmaceuticals industry or CRO preferably in clinical monitoring. Other experience may also be relevant, e.g. as study staff at a clinical research site.
• Knowledge of Good Clinical Practice (GCPs), ICH Guidelines, and local regulations, research process and scientific knowledge as relates to clinical trial conduct.
• Willingness to travel

About the department

In CMRQ (Clinical Medical Regulatory and Quality),We commit to bringing our products to Chinese market with the fastest speed and top quality, and applying the most scientific way to communicate our products benefits to our customers. We have 6 team in CMRQ aiming to portfolio evaluation and overall strategy New product approval, licence maintenance, Product localization Clinical evidence trial operation Phase (I-IV, NIS) Multiple stakeholders engagement (HA/KOLs/investigators) and Medical evidence generation/communication.

Working at Novo Nordisk

At Novo Nordisk we recognise that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and the communities we operate in.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to discuss flexible working, depending on the role and subject to business needs.

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

At Novo Nordisk, we're not chasing quick fixes - we're creating lasting change for long-term health. For over 100 years, we've 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 what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're 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.