Clinical Research Coordinator
Core
Coordinate care for patients on clinical research protocols and manage the implementation of Phase 4 and observational/registry trials under medical supervision.
Role type
Clinical Research Coordinator (non-RN)
Builds
Clinical trial data and patient care processes for oncology and hematology studies
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Protocol comprehension, GCP/ICH/FDA regulatory knowledge, adverse event reporting, informed consent process, data collection and integrity, investigational product handling, budget execution
Preferred skills
College education, prior research or medical science experience, EMR experience, EDC experience, CTMS experience
Technologies
MS Office (Word, Excel, PowerPoint, Outlook), EMR, EDC, CTMS
Responsibilities
Conduct protocol feasibility assessments, identify and screen study subjects, review diagnostic tests, document adverse events, ensure proper storage and handling of investigational products, collect and report accurate data, prepare documents for monitoring visits
Seniority
Entry-level, foundational
