Research Nurse (31089)

Physician Affiliate Group of New York • Bronx, NY

5d • Onsite

About The Position

Physician Affiliate Group of New York (PAGNY) is hiring a Research Nurse at NYC Health + Hospitals/Jacobi and North Central Bronx. The role coordinates and provides clinical nursing care to research participants in accordance with approved study protocols, Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements.

The Research Nurse administers and documents investigational medications and study-related treatments, monitors participants for treatment responses and safety concerns, and performs protocol-required clinical procedures and assessments. The position collaborates with investigators and clinical and research teams on participant eligibility, informed consent, study visits, and continuity of care. It also maintains source documentation, electronic medical records, and research data, and supports sponsor monitoring visits, audits, and other research activities.

PAGNY directly employs nearly 4,000 physicians and allied health professionals who provide services to NYC Health + Hospitals. The organization describes its mission as providing accountable, responsive, quality care with sensitivity to the needs of New York City's diverse population.

Requirements

• Bachelor of Science in Nursing (BSN).
• Current New York State Registered Nurse (RN) license.
• At least 3 years of nursing experience.
• Experience with medication administration, IV therapy, patient assessments, and clinical monitoring.
• Strong organizational, communication, documentation, and clinical assessment skills.
• Proficiency with electronic medical records and Microsoft Office applications.

Nice To Haves

• Nursing experience in clinical research is preferred.
• Knowledge of Good Clinical Practice (GCP), clinical research protocols, and regulatory requirements is strongly preferred.

Responsibilities

• Coordinate and provide clinical nursing care to research participants in accordance with approved study protocols, GCP, institutional policies, and regulatory requirements.
• Administer and document investigational medications and study-related treatments, including oral, subcutaneous, intramuscular, and intravenous medications, according to approved protocols, authorized orders, and nursing scope of practice.
• Monitor participants for treatment responses, adverse events, and other safety concerns; document and report concerns promptly to 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 informed consent, 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.

Benefits

• 401(k): immediate vesting in a 3% company contribution of base earnings; after one year of service, an additional 7% company contribution. No employee match is required.
• Generous annual paid time off, including vacation and holidays.
• Medical, prescription, and dental coverage.
• Life insurance and accidental death and dismemberment coverage equal to 3 times salary, up to $250,000, provided at no cost; voluntary employee-paid coverage is also available.
• Healthcare and dependent care flexible spending accounts.
• Pre-tax employee-paid contributions for commuting expenses.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level