Job Description

We are seeking a skilled and compassionate Research Nurse in Staten Island to support patient-centered clinical trials in compliance with established protocols and regulatory guidelines. This role involves direct patient interaction, coordination with interdisciplinary teams, and meticulous documentation to ensure the integrity of clinical research activities.

Key Responsibilities

Contribute to the initial assessment of research protocols, evaluating feasibility based on site capacity, patient population, and clinical criteria.

Partner with Principal Investigators (PIs) to screen and determine subject eligibility, accurately documenting findings according to study requirements.

Guide patients and families through the informed consent process, ensuring ongoing understanding and compliance with FDA, GCP, IRB, and sponsor regulations.

Educate participants, caregivers, and internal healthcare staff on study specifics, protocol changes, and emerging clinical data.

Perform essential clinical procedures such as phlebotomy, vital signs, specimen collection, ECGs, IV insertion, and investigational drug administration under appropriate supervision.

Support audits and inspections by regulatory authorities and sponsors through preparation and facilitation of site documentation and data review.

Assist in the evaluation of clinical response to treatment, collaborating with the PI to assess outcomes and ensure protocol adherence.

Aid in the coordination and administration of study budgets and grant submission processes in collaboration with study leadership.

Maintain accurate, timely, and compliant records of all clinical trial activities and patient interactions.

Carry out other related clinical research duties as needed.

Required Skills & Experience

Solid understanding of Good Clinical Practice (GCP) standards

Experience with regulatory submissions (IRB, ethics committees)

Proficient in conducting patient follow-ups and sample processing

Skilled in site qualification visit (SQV) preparation and study start-up

Strong interpersonal and communication abilities

Able to work independently and collaboratively within a multidisciplinary team

Adaptable and quick to learn within a dynamic research environment

Additional Details

Open to Relocation: Yes

Seniority Level: Intermediate to Entry-Level

Work Authorization: Must be authorized to work in the United States

Job Tags

Similar Jobs