Sr. Clinical Research Associate

Clinical, Medical & Regulatory (CMR) department

Vancouver, British Columbia

Are you passionate about clinical research and have a proven track record in Clinical Research ? Do you want to play a key role in driving clinical research that make a real difference in patients’ lives? If so, we invite you to join our team in Canada. Read on and apply today!

Your new role

As part of the Sr. Clinical Research Associate team, you will:

• Lead the planning, execution, and summarisation of clinical trial activities for assigned investigative sites.

• Ensure strict adherence to protocols, ICH-GCP guidelines, Health Canada regulations, local ethics requirements, and Novo Nordisk SOPs.

• Act as the primary point of contact for clinical sites, fostering collaborative relationships while ensuring data quality and subject safety.

• Develop and implement patient recruitment and retention strategies, analysing enrolment projections to meet trial targets and milestones.

• Provide leadership by mentoring less experienced CRAs and contributing to internal process improvement initiatives.

Your new department

The Clinical, Medical & Regulatory (CMR) team in Canada is at the forefront of driving innovation in clinical research. With a focus on collaboration and excellence, we manage projects that are critical to advancing Novo Nordisk’s mission of defeating serious chronic diseases. Our team operates in a fast-paced and dynamic environment, ensuring consistency across clinical trials while adhering to the highest standards of quality and compliance. Joining CMR means being part of a supportive and ambitious group of professionals dedicated to making a difference for patients worldwide.

Your skills and qualifications

We are looking for a candidate with the following qualifications:

• Must-Have Skills
  • At least a minimum of 6 years of clinical trial experience within pharmaceutical and/or healthcare setting of which at least 4 years has been in the role of an on-site monitoring CRA
  • Previous experience as a Study Coordinator is an asset
  • ICH/GCP experience
• Nice-to-Have Skills
  • Bilingual proficiency in French and English to support trials in all Canadian regions.
  • Possession of a formal CRA/Monitoring training certificate or prior experience as a Study Coordinator.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

More information

For more information, visit novonordisk.com, Facebook, Instagram, X, LinkedIn and YouTube.

To complete your application, click on "Apply now", attach your CV and follow the instructions.

Deadline

Please apply before October 14th, 2025

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

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

"Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.”