Senior Clinical Research Associate – Oncology, Hematology

• Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits
• Provide mentoring and guidance to less experienced CRAs and site staff when needed
• Document site visit findings via written reports
• Assess, monitor, and train study site staff on protocol adherence
• Review study subject safety information and informed consent
• Conduct source document verification for compliance, patient safety, and data veracity
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution
• Provide updates for site-related documentation for filing in the Trial Master File (TMF)
• Ensure site compliance with investigational product receipt, accountability, and return or destruction
• Conduct accompanied site visits for assessment or training of other CRAs

• Excellent interpersonal, oral, and written communication skills in French and English
• Superior organizational skills with attention to details
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS and EDC Systems
• 5+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Willingness to travel required

• Diverse and inclusive work environment
• Supportive and cohesive teams
• Accessible leadership
• Professional growth and development opportunities
• Mentoring and guidance from experienced leaders and CRAs