Entry-level Clinical Research Associate - Clinical Research Coordinator experience
Core
Conduct on-site monitoring visits for clinical trials of drugs and medical devices to ensure data accuracy and regulatory compliance.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical trial monitoring, regulatory compliance (GCP/SOPs), medical record verification, adverse event reporting, site qualification, patient recruitment assessment, inventory management
Preferred skills
Background in nursing, dietetics, pharmacy, biomedical research, or sales
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; Monitor adverse events and protocol deviations; Assess patient recruitment and retention; Maintain drug/device inventory
Seniority
Entry-level, training-focused IC
