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
• Update 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 English
• Superior organizational skills with attention to details
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS and EDC Systems
• 2+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Experience in Oncology and Hematology is required
• Willingness to travel required

• Supportive and team-oriented work environment
• Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
• Diverse and inclusive workplace
• Equal employment opportunities