Drive strategic solutions in real-world evidence with Novo Nordisk as the Associate Director in Mississauga. Lead a dedicated team across creative 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 StrategyManage and mentor a team of RWE professionalsLead local studies including clinical and observational researchCollaborate with stakeholders for innovative solutionsEnsure compliance with regulatory and quality standardsRequirements:PhD, Masters, MD, or PharmD in healthcare-related fieldExperience in innovative trials and RWE studiesStrong knowledge in healthcare data applicationsProven people management experienceExcellent collaboration in a cross-functional environmentLeverage 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