Nurse Practitioner​/Physician Assistant – Sub-Investigator

Responsibilities

• Perform Physical Exams
• Assess Lab Values and Evaluate EKGs
• Monitor Subject Compliance with study drug use and follow-up visits
• Evaluate Subject Response to therapy
• Document Adverse Events and determine their relationship to treatment
• Provide Medical Care for treatable adverse events
• Communicate with Primary Care Physicians about subject participation if requested
• Record Study Events in subject’s source documents
• Report Serious Adverse Events promptly to the PI and study coordinator
• Familiarize with Investigational Products and related documents
• Effective Communication with subjects, research team, IRB, and sponsors
• Regular Team Meetings to discuss subject participation, issues, and protocol processes
• Other Duties as Assigned

• Must hold a valid and current Advanced Practice Registered Nurse (APRN) and Certified Nurse Practitioner (CNP) license in Texas.
• Commitment to Ethical Research Practices and patient safety
• Experience with CTMS a plus
• No History of License Suspension or debarment in any state or by the FDA
• Clinical Experience working with patients
• IV Certification a plus

Demonstrates expertise in conducting physical exams, evaluating lab values, and monitoring patient compliance in clinical research settings. Proficient in documenting adverse events and communicating effectively with healthcare teams and subjects.