Entry-level Clinical Research Associate - Clinical Study Coordinator experience required
Core
Conduct on-site monitoring visits for clinical trials to ensure data accuracy, protocol compliance, and patient safety across global research sites.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device development
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Clinical research coordination, site monitoring, regulatory compliance, data verification, patient recruitment assessment, adverse event reporting, inventory management
Preferred skills
Medical or health science background, travel adaptability, Microsoft Office proficiency
Technologies
Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC)
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Monitor adverse events and concomitant medications; Assess patient recruitment and retention; Maintain regulatory document inventory
Seniority
Entry-level, requires prior coordinator experience
