Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred
Core
Manage oncology patients participating in pharmaceutical-sponsored clinical trials, handling screening, enrollment, education, and monitoring to ensure protocol and regulatory compliance.
Role type
Clinical Research Coordinator (Phase II-III)
Builds
Clinical trial data and patient safety outcomes for pharmaceutical sponsors
Domain
Oncology / Clinical Research
Deliverable
client delivery
Required skills
Patient screening and enrollment, Good Clinical Practice (GCP) knowledge, FDA regulations compliance, informed consent management, regulatory compliance monitoring, data documentation, drug dosing calculations (BSA, ANC), multidisciplinary team liaison
Preferred skills
Registered Nurse (RN) certification, complex data analysis, technical document interpretation
Technologies
Computer applications (word processing, email)
Responsibilities
Recruit and screen potential clinical trial subjects, Conduct detailed review of patient medical history for eligibility, Educate patients on study protocols and medication adherence, Maintain patient safety and rights throughout the study, Interface with multiple departments including Physicians and Pharmacy, Document all relevant patient and study information accurately
Seniority
Entry to Mid-level, hands-on IC
