Clinical Research Associate (CRA) - Oncology & General Medicine

We are seeking Experienced Clinical Research Associates (CRAs) to lead and support a Full Service Outsourcing team across various sponsors, with a focus on Oncology or Ophthalmology. French-speaking candidates are preferred, and location flexibility across Canada is offered. The role involves conducting 8-10 documentation oversight visits per month, with potential travel nationwide. Key Responsibilities Include Managing all aspects of site monitoring, including routine visits, site close-out, and liaising with vendorsEnsuring protocol adherence, proper informed consent procedures, and data integrityHandling registry management, SAE reporting, and source document reviewSupporting site staff training and acting as a local project coordinator as neededPerforming tasks independently and assisting in training new team members Qualifications And Skills University, college, or allied health certification (e.g., nursing license)1+ years of clinical monitoring experience, preferably in Oncology or OphthalmologyCAR-T experience is highly desiredComfort working in a fast-paced, dynamic environment with changing prioritiesStrong teamwork, communication, and technology skillsAbility to travel and perform physical activities related to site visits Work Environment And Physical Requirements Office-based with frequent travel across CanadaAbility to operate computers, lift up to 20 lbs, and perform related physical tasksConsistent attendance and adaptability to varied hours This role emphasizes high-quality clinical oversight, data accuracy, and effective communication within a collaborative, technology-driven environment.