Clinical Research Coordinator III (Nurse - Phase 1)
Core
Coordinate patient management and execution of Phase 1 clinical trials for drug development, including recruitment, safety monitoring, and data collection.
Role type
Senior clinical research nurse (Phase 1 trials)
Builds
Clinical trial protocols and patient care plans for pharma-sponsored and investigator-initiated studies
Domain
Oncology / Clinical Research
Required skills
Patient recruitment and screening, Informed consent administration, Clinical trial protocol execution, Adverse event monitoring, Vital signs and ECG monitoring, Medication administration, Sample collection and processing, Data collection and source documentation, ICH/GCP guidelines knowledge, Chemotherapy administration
Preferred skills
ACRP or SOCRA certification, deSouza Institute chemotherapy certification, IATA shipping regulations knowledge, Laboratory procedures knowledge, MS Office proficiency
Responsibilities
Identify and screen potential study subjects, Obtain informed consent, Coordinate patient visit schedules, Execute study visits including assessments and sample collection, Monitor patient safety and adverse events, Administer treatments per protocol, Collect and document clinical data
Seniority
Mid-Senior, hands-on IC