The Senior Clinical Research Associate is responsible for delivering high-quality site management and monitoring for clinical studies to ensure scientific quality and ethical standards
Job Summary
The Senior Clinical Research Associate is responsible for delivering high-quality site management and monitoring for clinical studies to ensure scientific quality and ethical standards.
This role involves conducting on-site and remote monitoring visits, driving recruitment, and developing strong relationships with investigators and site staff.
Candidates must be able to travel up to 60% and work in a fast-paced environment that values diversity and continuous improvement.
Matching Summary
The Senior Clinical Research Associate is responsible for delivering high-quality site management and monitoring for clinical studies to ensure scientific quality and ethical standards.
Skills & Requirements
Must-have
5+ years clinical research experience
4+ years site management monitoring
Bachelor's degree in life sciences
Knowledge of GCP and regulatory guidelines
Proficiency with Microsoft Office Suite
Nice-to-have
Experience with peripheral vascular diseases
Medical device study background
Veeva Vault CTMS proficiency
ACRP or SOCRA certification
Strong interpersonal communication skills
Key Requirements
Bachelor's Degree (BS/BA) in life sciences
5+ years experience in clinical research
4+ years experience with site management & monitoring
Valid knowledge of domestic and international regulations