Senior Clinical Research Associate I (SCRA I)
Core
Oversee site management, monitoring, and close-out operations for clinical trials, ensuring compliance and patient safety while mentoring junior CRAs.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical trials
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical trial monitoring, GCP/ICH regulations, site activation management, issue resolution, CAPA implementation, regulatory inspection support, data analysis, stakeholder influence
Preferred skills
Oncology therapeutic experience, global clinical trial experience
Technologies
e-diary systems, database management tools
Responsibilities
Manage investigator sites from initiation to database lock, partner with Site Care Partners on feasibility and activation, mentor Clinical Research Associates, resolve complex site issues and manage CAPAs, support sponsor regulatory interactions, monitor site-level AEs/SAEs
Seniority
Senior, hands-on IC
