Sr Clinical Research Associate

Remote – US based candidates only, no visa sponsorship available

About the role

This role supports clinical priorities focused on quality, patient-centered outcomes, and effective care delivery. You will collaborate with clinical leaders, operational teams, and cross-functional stakeholders to improve standards, workflows, and execution. The position offers the opportunity to strengthen care quality, team performance, and measurable outcomes within a healthcare environment.

Responsibilities

• Support execution of clinical studies for product development and validation
• Collaborate cross-functionally to ensure timely monitoring and compliance
• Build professional relationships with investigators, site staff, and key opinion leaders
• Develop study documentation, conduct site selection, and train site personnel
• Coordinate data quality assurance with monitors and management teams
• Contribute to process improvements in study operational activities
• Perform site closeout and support study compliance monitoring

Requirements

• Bachelor's degree in a technical discipline; Master's or PhD preferred with relevant experience
• 5-8 years experience in clinical research; or 2-5 years with a Master's; or 0-2 years with a PhD
• Strong background in Good Clinical Practice (GCP) and clinical study execution
• Experience with electronic data capture systems (EDC), Clinical Trial Management Systems (CTMS), and electronic trial master files (eTMF)
• Preferred experience in diabetes clinical trials and Continuous Glucose Monitoring (CGM) systems
• Ability to manage multiple studies and drive efficiency in study operations

Benefits

• Exposure to innovative CGM technology and impactful patient communities
• Comprehensive benefits program
• Global growth and advancement opportunities
• Access to continual career development resources and tuition reimbursement
• Work within a forward-thinking organization focused on employee and community service

Pay

$100,700 – $167,900 annually