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Clinical Operations Associate Jobs in Vaughan, ON

TMF Associate Employment Type: Full time, Permanent Job Reports To ... Manager, TMF Operations Department/Unit Name : TMF Operations Job Summary: Responsible for the ...

... clinical excellence, system coordination, and compassionate support to ensure every child with ... Administrative & Operational Support * Provide senior administrative support to the Chief ...

Research Associate

Toronto, ON · On-site

CA$49.91 - CA$62.43/hr

A custom combination of technology and clinical expertise supports a reimagined model of care ... Your role will be to support the Research Chair in managing the day-to-day operations of the grant ...

Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to ... Clinical Affairs, Assay R&D, and Quality Assurance regarding priorities and timetables for ...

... operations while preserving clinical autonomy at the practice level. As Dentalcorp continues to ... The Associate Data Engineer will contribute to the development, support, and continuous improvement ...

Showing results 41-60

Clinical Operations Associate information

See Vaughan, ON salary details

$22

$44

$93

How much do clinical operations associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical operations associate in Vaughan, ON is $44.36, according to ZipRecruiter salary data. Most workers in this role earn between $28.88 and $54.13 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Vaughan, ON?

The most popular types of Clinical Operations jobs in Vaughan, ON are:

What cities near Vaughan, ON are hiring for Clinical Operations Associate jobs?

Cities near Vaughan, ON with the most Clinical Operations Associate job openings:

Infographic showing various Clinical Operations Associate job openings in Vaughan, ON as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $92,263 per year, or $44.4 per hour.

Associate Director, Real World Evidence

Novo Nordisk

Mississauga, ON • On-site

CA$159K - CA$209K/yr

Full-time

Re-posted 7 days ago


Novo Nordisk rating

8.2

Company rating: 8.2 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

32nd of 86 rated pharmaceutical


Job description

Medical and Regulatory Affairs

Mississauga, ON

Are you passionate about real-world evidence and its impact on healthcare? Do you have the expertise to drive innovative solutions and strategic alignment in clinical and real-world data? If so, we invite you to join us as our new Associate Director, Real World Evidence at Novo Nordisk. Read more and apply today!

Your new role

As the Associate Director, Real World Evidence, you will drive the development and execution of Real World Evidence Strategy and Evidence and Insights Generation Plans (EIGP) across all therapeutic area portfolios. In this role, you will report to the Head of Medical and Regulatory Affair and will be a member of the Medical and Regulatory Leadership Team. This is a people manager role; three team members will report to you.  Some of your specific responsibilities will include:

  • Provide strategic alignment of clinical and real-world data resources with business objectives. Support business cases for innovative solutions through presentations to management.
  • Lead and manage local studies, including RWE, clinical, and observational investigator-sponsored studies (ISS).
  • Manage and develop a team; set priorities, coach performance, and build RWE capabilities.
  • Collaborate with internal and external stakeholders, including key opinion leaders, RWE vendors, and global counterparts, to develop and implement innovative RWE solutions.
  • Scout and evaluate novel real-world data sources and methodologies to enhance insights and decision-making.
  • Ensure compliance with local regulatory requirements, Novo Nordisk policies, and quality standards.
  • Provide training and education on real-world evidence and clinical data sources as needed.

Your new department

As part of International Operations, you will join our largest operational unit. Covering 194 countries and 95% of the world's population, more than 18,000 of us work passionately to serve 35 million patients each day. With a promise to outperform the competition, we continue to be the growth driver for Novo Nordisk, and to improve health at scale across the globe.

Novo Nordisk is based in Mississauga, Canada, and this is an on-site position. At Novo Nordisk Canada, we are dedicated to driving evidence generation and insights that make a difference for patients and healthcare systems. Our team fosters a collaborative and innovative atmosphere, working together to address complex challenges and deliver impactful solutions. Join us in shaping the future of healthcare through real-world evidence.

 

Your Skills and Qualifications

We are looking for a candidate with the following qualifications:

  • A PhD, Masters, MD, or PharmD degree in a healthcare-related field (e.g., health economics, epidemiology, outcomes research, public health, biostatistics, medicine, biomedical sciences).
  • Strong knowledge and experience in designing innovative trials and real-world evidence studies.
  • Good knowledge of healthcare data and applications, pharmaceutical industry and clinical research.
  • Experience as a people manager, with direct reports.
  • Excellent collaboration skills and proven success working in a crossfunctional and matrix environment.

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

At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage. 

Salary: for this role the Annual Base salary ranges from $159,230 to $209,230.

The placement in the salary range will be assessed during the recruitment process based on your skills, competencies, knowledge and relevant experience match the position requirements.

Incentives: based on the role’s level and other factors, the salary package may include short-term (STI) and/or long-term (LTI) incentives.

Benefits: the eligibility for specific benefits may vary based on the job and location.

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.

This posting is not for an existing vacancy. 

Application Deadline: July 10th, 2026    -    We’re reviewing applications and interviewing as we go, which may allow us to conclude the process before the deadline. 

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.


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