Senior Clinical Research Associate
Core
Oversee and manage Phase I–III clinical trial activities to ensure compliance with protocol, regulatory requirements, and industry standards.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial execution across Oncology, Neurology, Psychiatry, Obesity, and Dermatology
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial monitoring, site management, regulatory compliance (ICH-GCP), data integrity management, study documentation management, issue resolution, training and guidance to site staff
Preferred skills
Proficiency in clinical trial software and tools, ability to manage multiple sites and projects simultaneously
Technologies
Clinical trial software and tools
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Manage study documentation, regulatory submissions, and ethics/IRB approvals; Collaborate with cross-functional teams to ensure high-quality data and patient safety; Ensure study cost efficiency and timely issue resolution
Seniority
Senior, hands-on IC
