Travel Research Associate
Core
Conduct clinical trial procedures at patient sites, manage patient care workflows, and ensure regulatory compliance for clinical research.
Role type
Clinical Research Associate (CRA) / Clinical Site Coordinator
Builds
Clinical trial data and patient care services for pharmaceutical/biotech clients
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
GCP compliance, vital signs measurement, phlebotomy, sleep study procedures, patient screening, data entry accuracy, equipment calibration, sample processing, regulatory documentation
Preferred skills
Sleep disorder education, consent management, freezer log maintenance, training new staff
Technologies
MS Office, clinical trial database systems
Responsibilities
Perform technical procedures including vital signs, ECG, and phlebotomy; conduct sleep study evaluations and apply sensors; interact with patients during study visits; manage clinical supplies and specimen labeling; report quality incidents; ensure adherence to GCP and local regulations
Seniority
Mid-level, hands-on IC
