Top Benefits
About the role
Sr. Clinical Research Associate
Category: Clinical Development
**Location:**Mississauga, Ontario, CA
Clinical, Medical & Regulatory (CMR) department
Mississauga, Ontario
Are you passionate about clinical research and ensuring patient safety? Do you have a strong background in monitoring clinical trials and fostering collaborative relationships with investigative sites? If so, we invite you to join our team as a Senior Clinical Research Associate at Novo Nordisk Canada. Take the next step in your career and apply today!
Your new role
As a Senior Clinical Research Associate, you will:
-
Implement, monitor, and summarise clinical trials while ensuring adherence to protocols, ICH-GCP, Canadian regulatory requirements, local ethics requirements, and Novo Nordisk SOPs.
-
Develop and maintain collaborative relationships with clinical investigative sites, ensuring data integrity, patient safety, and regulatory compliance.
-
Manage recruitment and retention strategies, analysing projections against actual numbers to meet targets.
-
Collaborate regularly with the study team, communicating site progress and escalating critical issues.
-
Perform on-site drug accountability and reconciliation, verifying drug storage and maintaining the Investigator Trial Master File (ITMF).
-
Participate in sponsor and regulatory audits, preparing sites and supporting external trial staff during audits.
-
Oversee operational aspects of clinical trials, including site and vendor selection, preparing clinical trial budgets, and ensuring studies are conducted within clinical trial protocols.
Your new department
You will be part of the Clinical, Medical & Regulatory (CMR) team in Canada. Our department is at the forefront of clinical development activities, from the initial planning of clinical trials to authority submissions. We investigate patient reactions to new drugs, compare them to existing products, and run pre-specified trials in human subjects. Our team provides expertise in Biostatistics, Clinical Reporting, Data Management, and more, ensuring process alignment, competency development, and knowledge sharing across trial management and medical staff. The atmosphere is dynamic, collaborative, and driven by a shared commitment to innovation and excellence.
Your skills and qualifications
We are looking for a candidate with the following qualifications:
- Must-Have Skills
- University graduate (BSc, Nursing Degree) or equivalent and minimum of 6 years of clinical trial experience within a pharmaceutical or healthcare setting.
- At least 4 years of experience as an on-site monitoring Clinical Research Associate (CRA).
- Strong understanding and experience with ICH-GCP.
- Nice-to-Have Skills
- CRA/Monitoring training certificate.
- Previous experience as a Study Coordinator.
- Bilingual (French and English).
- Ability to work effectively within international and local teams, work independently from home office and ability to prioritize tasks.
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 August 6th, 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.
About Novo Nordisk, Inc.
For almost 100 years, Novo Nordisk has been translating the unmet medical needs of people living with a serious chronic disease into innovative medicines and delivery systems, like our insulin pens.
Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases.
From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world.
Our industry is dynamic. And the scientific understanding of the diseases we treat and the people living with them, improves every day. This is a constant reminder that what got us to where we are today is not necessarily what will make us successful in the future.
As an employer, we recognise the need to embrace experimentation and strive for diversity and inclusion to help make better decisions by ensuring that multiple perspectives are considered.
Together, we’re life changing.
Top Benefits
About the role
Sr. Clinical Research Associate
Category: Clinical Development
**Location:**Mississauga, Ontario, CA
Clinical, Medical & Regulatory (CMR) department
Mississauga, Ontario
Are you passionate about clinical research and ensuring patient safety? Do you have a strong background in monitoring clinical trials and fostering collaborative relationships with investigative sites? If so, we invite you to join our team as a Senior Clinical Research Associate at Novo Nordisk Canada. Take the next step in your career and apply today!
Your new role
As a Senior Clinical Research Associate, you will:
-
Implement, monitor, and summarise clinical trials while ensuring adherence to protocols, ICH-GCP, Canadian regulatory requirements, local ethics requirements, and Novo Nordisk SOPs.
-
Develop and maintain collaborative relationships with clinical investigative sites, ensuring data integrity, patient safety, and regulatory compliance.
-
Manage recruitment and retention strategies, analysing projections against actual numbers to meet targets.
-
Collaborate regularly with the study team, communicating site progress and escalating critical issues.
-
Perform on-site drug accountability and reconciliation, verifying drug storage and maintaining the Investigator Trial Master File (ITMF).
-
Participate in sponsor and regulatory audits, preparing sites and supporting external trial staff during audits.
-
Oversee operational aspects of clinical trials, including site and vendor selection, preparing clinical trial budgets, and ensuring studies are conducted within clinical trial protocols.
Your new department
You will be part of the Clinical, Medical & Regulatory (CMR) team in Canada. Our department is at the forefront of clinical development activities, from the initial planning of clinical trials to authority submissions. We investigate patient reactions to new drugs, compare them to existing products, and run pre-specified trials in human subjects. Our team provides expertise in Biostatistics, Clinical Reporting, Data Management, and more, ensuring process alignment, competency development, and knowledge sharing across trial management and medical staff. The atmosphere is dynamic, collaborative, and driven by a shared commitment to innovation and excellence.
Your skills and qualifications
We are looking for a candidate with the following qualifications:
- Must-Have Skills
- University graduate (BSc, Nursing Degree) or equivalent and minimum of 6 years of clinical trial experience within a pharmaceutical or healthcare setting.
- At least 4 years of experience as an on-site monitoring Clinical Research Associate (CRA).
- Strong understanding and experience with ICH-GCP.
- Nice-to-Have Skills
- CRA/Monitoring training certificate.
- Previous experience as a Study Coordinator.
- Bilingual (French and English).
- Ability to work effectively within international and local teams, work independently from home office and ability to prioritize tasks.
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 August 6th, 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.
About Novo Nordisk, Inc.
For almost 100 years, Novo Nordisk has been translating the unmet medical needs of people living with a serious chronic disease into innovative medicines and delivery systems, like our insulin pens.
Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases.
From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world.
Our industry is dynamic. And the scientific understanding of the diseases we treat and the people living with them, improves every day. This is a constant reminder that what got us to where we are today is not necessarily what will make us successful in the future.
As an employer, we recognise the need to embrace experimentation and strive for diversity and inclusion to help make better decisions by ensuring that multiple perspectives are considered.
Together, we’re life changing.