Real World Evidence Associate Director
Real World Evidence Associate Director
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Job Description
Real World Evidence Associate Director
Clinical Development Medical and Regulatory Affairs (CMR)
Cardiovascular and Emerging Therapeutic Areas (CETA)
Toronto Canada
Are you passionate about transforming real-world data into actionable insights that shape healthcare decisions and business strategy Do you thrive at the intersection of science evidence and innovation If yes this is your opportunity to make an impact as Associate Director of Real World Evidence at Novo Nordisk.
Your new role
As Associate Director of Real World Evidence (RWE) you will provide strategic direction and expertise for clinical and real-world evidence across the Clinical Medical and Regulatory (CMR) department. You will be responsible for shaping and executing the Canadian evidence and insights generation plan (EIGP) across our therapeutic areas driving innovative RWE solutions and ensuring alignment with regional and global strategies. Acting as the Canadian lead for RWE within CMR you will build strong internal and external partnerships oversee local and global investigator-sponsored studies and deliver insights that shape business strategy. Some of your specific responsibilities will include:
Lead the development and implementation of the Canadian RWE strategy and Evidence & Insights Generation Plan across therapeutic areas within CMR.
Align clinical and real-world data resources with local regional and global strategic objectives.
Oversee design execution and governance of local RWE and observational studies including investigator-sponsored studies (ISS).
Collaborate cross-functionally with Clinical Development Medical Affairs Patient Access Commercial and Regulatory teams to maximize RWE impact.
Drive scouting and integration of novel real-world data sources ensuring high-quality and compliant data management.
Ensure compliance with Canadian regulatory requirements Novo Nordisk policies and audit readiness for all RWE activities.
Represent Canada in regional/global RWE initiatives working groups and strategic partnerships.
Your new department
As part of International Operations you will join our largest operational unit. Covering 194 countries and 95% of the worlds population more than 18000 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.
You will be part of the Clinical Medical & Regulatory (CMR) team at Novo Nordisk Canada and report to the Medical Director Cardiovascular and Emerging Therapeutic Areas. Our mission is to shape healthcare decisions through robust evidence innovative partnerships and patient-centered solutions.
Your skills and qualifications
We are looking for a candidate who possesses:
A PhD or Masters/MD/PharmD degree in appropriate healthcare-related field (heath economics epidemiology outcomes research public health business/health services research biostatistics medicine biomedical sciences) preferred.
Minimum 5 years of experience in Real-World Evidence (RWE) registries pragmatic trials or investigator-sponsored studies; Medical Affairs or Market Access experience is highly desirable.
Proven experience managing RWE studies with a strong commitment to data integrity and compliance.
In-depth knowledge of Canadian healthcare data clinical research and pharmaceutical industry applications.
Strong project management skills with the ability to lead cross-functional initiatives build stakeholder relationships and communicate effectively with both scientific and business audiences.
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.
Deadline
Please apply before October 06th 2025
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
Were not your typical healthcare 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.
Required Experience:
Director
Employment Type
Full Time
