Senior Clinical Research Associate I

About the role

As a Senior Clinical Research Associate (SCRA) you will be at the heart of our clinical operations-serving as the trusted liaison between our study teams and investigator sites. You will oversee the conduct of clinical trials from site activation through database lock, ensuring they meet the highest standards of quality, compliance, and patient safety. This is a role where your expertise directly impacts the integrity of clinical research and the development of life-changing therapies. Key accountabilities: Lead Site Operations: Manage all operational aspects of clinical trial activities at assigned investigator sites, ensuring timelines and quality deliverables are consistently met Build Strong Partnerships: Serve as the primary point of contact for investigator sites, fostering collaborative relationships with site personnel, study teams, and vendors Ensure Compliance & Safety: Conduct thorough site monitoring activities-both onsite and remote-to maintain protocol compliance and safeguard patient welfare Drive Quality & Resolution: Identify and resolve site issues promptly, develop corrective actions, and support quality event remediation Support Recruitment & Progress: Partner with study teams to facilitate investigator meetings, provide enrollment support, and drive recruitment initiatives Manage Critical Documentation: Submit timely reports, maintain trial master files, track protocol deviations, and monitor clinical supply management Mentor & Develop: May mentor Clinical Research Associates and coach site personnel on protocol requirements and best practices