As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects' rights, safety and well-being and quality of data compliance. Home-based in Quebec, Canada. You will: • Conduct and report all types of onsite monitoring visits • Be involved in study startup • Perform CRF review, source document verification and query resolution • Be responsible for site communication and management • Supervise study activities, timelines, and schedules on the country level • Be a point of contact for in-house support services and vendors • Be involved in quality control, such as compliance monitoring and reports review • Participate in feasibility research • Support regulatory team in preparing documents for study submissions Qualifications • College/University degree in Life Sciences or an equivalent combination of education, training & experience • Independent on-site monitoring experience • Experience in all types of monitoring visits in Phase II and/or III • Participation in clinical projects as a Lead/Senior Monitor • Experience in Oncology • Full working proficiency in English and French • Proficiency in MS Office applications • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel • Valid driver's license (if applicable) Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Videos To Watch https://www.youtube.com/watch?v=BZEQBN4wZGQ