Senior Clinical Research Associate managing oncology trial sites for Worldwide Clinical Trials, a global contract research organization. Overseeing study start-up, site maintenance, safety reporting, and closeout across Canada.
Responsibilities
Manage research activities at sites participating in Worldwide’s clinical research projects
Identify potential sites to participate in clinical research
Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations
Train sites to collect data properly and report potential safety-related events
Manage site activities during study maintenance
Close down research activities at sites once studies conclude
Conduct study initiation visits (SIVs)
Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements
Collaborate with colleagues across diverse therapeutic areas and specialties
Requirements
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
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 Nursing Degree
Experience in Oncology is required
Candidates must reside in Canada
Willingness to travel regionally required
Benefits
Extensive support through regulatory submissions, TMF management, and in-house CRAs
Regular touchpoints and coaching conversations with the Line Manager
Clear career path and professional development leading to Clinical Trial Manager roles
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