Associate Director, Real World Evidence

Novo Nordisk
Location
Mississauga, Ontario, CA
Job Type
Full-time
Posted
September 24, 2026
Views
48
Salary Range
$159k - $209k USD

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.

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.

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The position is located in Mississauga, Ontario, CA, and is an on-site position.
What are the key responsibilities of this role?
You will drive the Real World Evidence Strategy and Evidence and Insights Generation Plans. Responsibilities include leading local studies, managing and developing a team of three, collaborating with stakeholders, scouting novel data sources, and ensuring compliance with local regulatory requirements and Novo Nordisk policies.
Who will I report to and will I manage a team?
You will report to the Head of Medical and Regulatory Affairs and be a member of the Medical and Regulatory Leadership Team. This is a people manager role with three team members reporting directly to you.
What qualifications and experience do I need to apply?
You need a PhD, Masters, MD, or PharmD in a healthcare-related field. You must have strong knowledge and experience designing innovative trials and RWE studies, good knowledge of healthcare data and the pharmaceutical industry, experience as a people manager with direct reports, and excellent collaboration skills.
What is the salary range for this position?
The annual base salary ranges from $159,230 to $209,230. Your placement within this range will be assessed during the recruitment process. Depending on the role's level, the package may also include short-term and/or long-term incentives.
What is the application process and deadline?
To apply, click "Apply now", attach your CV, and follow the instructions. The application deadline is July 10th, 2026. Note that applications are reviewed and interviews are conducted on an ongoing basis, which may conclude the process before the deadline.

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Source: manual
AI Relevance: 78/100 (Relevant)
Remote Type: onsite
Allowed Locations: Worldwide
Skills & Tags:
novo nordisk biostatistics clinical
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