Clinical Research Coordinator III (Phase 1)
Core
Coordinate patient management and execution of Phase 1 clinical trials for the Drug Development Program, including recruitment, safety monitoring, and data collection.
Role type
Senior Clinical Research Coordinator (Phase 1 Oncology)
Builds
Clinical trial data and patient care outcomes for pharma-sponsored and investigator-initiated studies
Domain
Oncology / Clinical Research / Drug Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Patient recruitment and screening, Informed consent administration, Vital signs and ECG monitoring, Medication administration per protocol, Sample collection and processing, Data collection and source documentation, Adverse event monitoring, Chemotherapy administration
Preferred skills
ACRP or SOCRA certification, DeSouza Institute Chemotherapy certification, IATA shipping regulations knowledge, Laboratory procedures knowledge
Technologies
MS Office (Word, Excel, PowerPoint)
Responsibilities
Identify and screen potential study subjects, Execute study visits including assessments and sample collection, Monitor patient safety and administer treatments, Coordinate patient visit schedules, Provide clinical care and patient/family teaching, Ensure meticulous documentation per ICH/GCP guidelines
Seniority
Mid-to-Senior, hands-on IC