Nurse Practitioner/Physician Assistant Sub-Investigator, On-Site, Phoenix, AZ
Core
Mid-level provider (Nurse Practitioner or Physician Assistant) performing clinical assessments, monitoring patient compliance, and managing adverse events in clinical research studies.
Role type
Mid-level provider sub-investigator (clinical research)
Builds
Clinical research data and patient safety reports for life sciences sponsors
Domain
Clinical research / Healthcare
Required skills
Physical exams, lab value assessment, EKG evaluation, adverse event documentation, medical care for adverse events, study protocol adherence, source document recording, regulatory compliance (IRB/FDA)
Preferred skills
CTMS experience, IV certification
Technologies
CTMS
Responsibilities
Perform physical exams, assess lab values and evaluate EKGs, monitor subject compliance with study drug use, evaluate subject response to therapy, document adverse events, provide medical care for treatable adverse events, communicate with primary care physicians, record study events in source documents, report serious adverse events to PI, familiarize with investigational products, conduct regular team meetings
Seniority
Mid-level, hands-on IC
