Drive strategic solutions in real-world evidence with Novo Nordisk as the Associate Director in Mississauga. Lead a dedicated team across innovative clinical data projects and evidence generation plans.

In this pivotal role, you will report to the Head of Medical and Regulatory Affairs and oversee a team of three. Your expertise will align clinical data resources with business objectives while engaging with key stakeholders and managing local studies. This leadership position requires collaboration with internal and external partners to enhance decision-making through novel data insights.

Key Responsibilities:



• Develop and execute Real World Evidence Strategy • Manage and mentor a team of RWE professionals • Lead local studies including clinical and observational research • Collaborate with stakeholders for creative solutions • Ensure compliance with regulatory and quality standards

Requirements: • PhD, Masters, MD, or PharmD in healthcare-related field • Experience in creative trials and RWE studies • Strong knowledge in healthcare data applications • Proven people management experience • Excellent collaboration in a cross-functional setting

Leverage your skills in evidence generation and team leadership to impact healthcare outcomes at Novo Nordisk. J-18808-Ljbffr

📌 Associate Director Real World Evidence Mississauga
🏢 Novo Nordisk
📍 Mississauga