Senior Clinical Research Associate – CNS

Job Description:

• Manage research activities at sites participating in Worldwide’s clinical research projects
• Identify potential sites to participate in research efforts
• Perform study start-up activities, including collecting regulatory documents from sites
• Support negotiation of contracts and budgets
• 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 requirements, safety-event reporting, and applicable regulatory requirements

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 CNS is strongly preferred
• Candidates must reside on the West Coast
• Willingness to travel regionally required

Benefits:

• Support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
• Regular touchpoints and coaching conversations with Line Manager
• Clear career path and professional development that can lead to Clinical Trial Manager roles
• Accessible Executive Leadership team
• Competitive benefits package depending on location
• Transparent compensation and pay equity