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Job description
Job Title: Nurse Practitioner Clinical Research
Location: On-Site
Job Type: Full-Time, W2
Schedule: Monday - Friday: 8 AM - 5 PM
Job Summary:
The Nurse Practitioner (NP) Clinical Research plays a key role in the planning, coordination, and execution of clinical research studies. Working closely with physicians, researchers, and study sponsors, the NP ensures the delivery of high-quality patient care while supporting clinical trial protocols. This position bridges clinical expertise and research integrity, ensuring compliance with regulatory requirements and contributing to advancements in medical science.
Key Responsibilities: Conduct physical exams, obtain medical histories, and assess eligibility of patients for clinical trial participation.
Administer investigational products (as permitted), monitor patients for adverse events, and provide follow-up care in accordance with study protocols.
Collaborate with Principal Investigators (PIs) to ensure protocol adherence and accurate documentation of patient assessments and clinical trial data.
Educate study participants on the clinical trial process, including informed consent, procedures, and potential risks and benefits.
Monitor patient safety, manage side effects, and report adverse events to the study team and regulatory bodies as required.
Maintain accurate and complete source documentation and assist in data collection and entry into electronic data capture systems.
Participate in study initiation, monitoring, close-out visits, and audits/inspections by sponsors and regulatory agencies.
Support recruitment and retention strategies for study participants.
Ensure compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and federal and state regulations.
Qualifications: Master s or Doctorate degree in Nursing from an accredited program.
Current Nurse Practitioner licensure in good standing.
Board certification as a Nurse Practitioner (e.g., FNP, AGNP, etc.).
Minimum of 1 3 years of experience in a clinical research setting preferred.
Clinical experience in the relevant therapeutic area (e.g., oncology, cardiology, infectious diseases) may be required or preferred depending on the position.
Strong knowledge of clinical trial processes, GCP guidelines, and human subjects protection.
Excellent communication, organizational, and problem-solving skills.
Ability to work independently and as part of a multidisciplinary research team.
Worksite address
san antonio, TX, 78201, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.