Drive clinical excellence at Worldwide Clinical Trials as a Senior Clinical Research Associate. This position is key to managing oncological research sites and ensuring compliance with regulations.You will leverage your five-plus years of CRA experience to oversee research activities across clinical trial sites. Your role will involve site selection, data training, and compliance checks during the study lifecycle. Your commitment to quality in clinical operations will directly affect patient outcomes in various disease areas.Key Responsibilities:Oversee research activities at participating clinical sitesConduct study initiation visits for compliance assuranceTrain site personnel on data collection processesManage budgets and negotiate site contractsEnsure proper closure of research sites after studiesRequirements:5+ years as a Clinical Research Associate requiredBachelor's or Nursing degree essentialExperience in Oncology requiredFluent in both English and FrenchMust reside in Canada and have the ability to travelUtilize your communication and organizational skills to support impactful clinical research with Worldwide Clinical Trials.

📌 Senior Clinical Research Associate Canada (Quebec City)
🏢 Worldwide Clinical Trials
📍 Quebec City