Research Nurse (31089)

Physician Affiliate Group of New York (PAGNY) has an opportunity for a Research Nurse at NYC Health + Hospitals/Jacobi and North Central Bronx. Jacobi Medical Center is a 457-bed, Level I Trauma Center and North Central Bronx Hospital (NCB) has 213 licensed beds. To this day, Jacobi and NCB remain respected leaders in emergency medicine, trauma surgery, burn care, pediatrics, primary care, and women’s health. The hospital maintains a strong academic affiliation with Albert Einstein College of Medicine to maintain its high healthcare delivery standards.

The mission of NYC Health + Hospitals is to extend equally to all New Yorkers, regardless of the ability to pay, comprehensive health services of the highest quality in an atmosphere of humane care, dignity, and respect. Their Values are built on a foundation of social and racial equity and has established the ICARE standards for all staff.

NYC Health + Hospitals is the nation’s largest municipal health care delivery system in the United States. Dedicated to providing the highest quality health care services to all New Yorkers with compassion, dignity and respect, and regardless of immigration status or ability to pay.

Opportunity Details:

• Responsible for coordinating and providing clinical nursing care to research participants in accordance with approved study protocols, Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements.
• Administer and document investigational medications and study related treatments including oral, subcutaneous, intramuscular, and intravenous medications, in accordance with approved protocols, authorized orders, and nursing scope practice.
• Monitor participants for treatment responses, adverse events, and other safety concerns, ensuring timely documentation and reporting to the appropriate study personnel.
• Perform clinical procedures, including vital sign monitoring, venipuncture, IV catheter placement, blood draws, specimen collection, and other protocol-required assessments.
• Collaborate with investigators to assess patient eligibility and facilitate the informed consent process, as applicable.
• Coordinate study visits, clinical procedures, and laboratory testing.
• Maintain accurate and timely source documentation, electronic medical records, and research data in accordance with protocol and regulatory requirements.
• Collaborate with investigators, research coordinators, pharmacists, and clinical teams to ensure protocol compliance and continuity of care.
• Support sponsor monitoring visits, audits, and other research related activities.