Clinical Research Coordinator I
Core
Coordinate oncology clinical trials (Phase I-III) for the Clinical Research Management Office, managing patient enrollment, data collection, and regulatory compliance.
Role type
Clinical Research Coordinator
Builds
Clinical trial operations for oncology studies
Domain
Healthcare / Oncology Clinical Research
Deliverable
client delivery
Required skills
Clinical trial coordination, informed consent documentation, patient scheduling, specimen collection, CTMS data entry, adverse event reporting, regulatory compliance (GCP/HIPAA)
Preferred skills
3-5 years clinical research experience, scientific or health-related degree
Technologies
Clinical Trials Management System (CTMS)
Responsibilities
Obtain and document informed consent, schedule study procedures and assessments, coordinate specimen collection, update CTMS with patient data, document and report serious adverse events, facilitate sponsor meetings, liaise with hospital staff and auditors
Seniority
Mid-level IC
