Senior Clinical Research Associate

• 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 applicable 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 as requested and appropriate

• 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 RN/BSN in Nursing
• Willingness to travel required

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law
• Diverse and inclusive work environment
• Supportive teams and accessible leadership
• Opportunities for professional growth and development