Location & Practice Overview

The position is based within Adams Clinical’s New York City research sites, with required presence at both the Harlem and Bronx locations.

Practice Type Independent clinical trial site network conducting pharmaceutical-sponsored studies
Harlem Site 345 E 102nd Street, Suite 200 (D), New York, NY 10029
Bronx Site 1200 Waters Place, Suite 310, Bronx, NY 10461
Care Setting Outpatient research clinics; Bronx site also supports inpatient psychiatry capabilities

Responsibilities

  • Place IVs, initiate and manage infusions per sponsor protocol, and assist with difficult phlebotomy or IV access.
  • Administer subcutaneous and intramuscular injections.
  • Review medical records and laboratory results; reconcile concomitant medications.
  • Collect adverse events and medical history; report serious adverse events with required follow-up.
  • Facilitate informed consent, perform screening procedures, enter study data, and maintain regulatory binders.
  • Provide on-site medical support for emergencies and mentor clinical research coordinators.

All activities occur under the supervision of physician principal investigators and the clinical nurse manager in accordance with FDA regulations and GCP.

Qualifications & Requirements

Core credentials are required; prior research experience is preferred rather than mandatory.

License
Active Registered Nurse license in New York State
Education
Bachelor’s degree in nursing
Nursing Experience
Two or more years preferred; recent bedside experience viewed as ideal
Research Experience
Preferred but not required
Site Availability
Ability to work at both New York City locations

Compensation & Benefits

Salary is set between $90,000 and $110,000 per year, commensurate with experience, and is paired with a standard benefits package.

  • $90,000–$110,000 annual salary
  • 401(k) matching
  • Medical, dental, and vision insurance
  • Health savings account, flexible spending account, and life insurance
  • Paid time off and parental leave
  • Employee assistance program and professional development assistance

Schedule & Work Environment

Employment Type Full-time
Work Model On-site
Site Structure Regular presence required at both Harlem and Bronx research sites
Physical Setting Research clinic environment supporting scheduled participant visits

Patient Population & Clinical Setting

The nurse works with adult participants enrolled in pharmaceutical-sponsored clinical trials. Studies at the New York sites commonly address psychiatric and neurological indications.

Participant Type Adults enrolled in industry-sponsored research protocols
Study Focus Areas Psychiatric and neurological conditions; specific indications vary by active protocol
Visit Structure Scheduled research visits rather than unscheduled acute care encounters
Setting Character Protocol-governed research environment distinct from routine clinical practice

Clinical Focus & Key Services

The clinical content of the role centers on the safe delivery and monitoring of investigational products within defined study protocols.

Investigational Product Administration IV infusions and injectable study medications delivered according to sponsor instructions
Safety Surveillance Ongoing assessment and documentation of adverse events and serious adverse events
Clinical Data Review Laboratory results, medical history, and medication reconciliation supporting protocol compliance
Regulatory Framework All clinical activity conducted under FDA regulations and Good Clinical Practice standards

Role Highlights

Distinctive features of this position relative to many clinical research nursing roles.

  • Dual-site operational model spanning two separate New York City research clinics
  • Formal mentoring and guidance responsibilities for clinical research coordinators
  • Combination of advanced vascular-access skills with structured research-operations duties

About Adams Clinical

Adams Clinical is an independent clinical research site network specializing in late-phase psychiatric and neurologic trials. Founded in 2011 and headquartered in Watertown, Massachusetts, the organization currently operates six locations across New York, Massachusetts, Pennsylvania, and Texas. The New York City sites are located in Harlem and the Bronx. The network has contributed to studies supporting the development of multiple approved medications in psychiatry and neurology.

Organization Type Independent clinical research site network
Founded 2011
Headquarters Watertown, Massachusetts
Network Scale Six sites in four states
Primary Focus Late-phase psychiatric and neurologic clinical trials

Frequently Asked Questions

Is this primarily a clinical care role or a research role?
The position blends hands-on nursing procedures with protocol-driven research operations. Participant interactions occur within the framework of specific study protocols rather than general clinical treatment plans.
Will I need to work at both the Harlem and Bronx sites?
Yes. The role requires the ability and willingness to work at both New York City locations as part of normal duties.
Is prior clinical research experience mandatory?
No. Research experience is preferred but not required. Recent bedside nursing experience is considered particularly relevant.
Who provides clinical supervision?
The Clinical Research Nurse works under the supervision of physician principal investigators and the clinical nurse manager.
Does the position include mentoring other staff?
Yes. Clinical research nurses provide mentoring, direction, and guidance to clinical research coordinators.
Are the trials mainly outpatient?
Most activity occurs in outpatient research clinic settings. The Bronx site also maintains inpatient psychiatry capability for certain studies.

Clinical Research Nursing Environment in New York City

Clinical research nursing at Adams Clinical combines direct participant care with the structured workflow of pharmaceutical-sponsored studies. Rather than following a general inpatient or outpatient treatment plan, the nurse works within study-specific protocols that define visit procedures, investigational product administration, safety assessments, documentation, and required follow-up. A typical research workflow can involve preparing a participant for a scheduled study visit, reviewing relevant medical information and laboratory results, completing protocol-required nursing procedures, documenting findings, and communicating clinically important information to the study team. The role therefore requires both hands-on nursing judgment and consistent attention to protocol details and research documentation. Clinical Research Nurses also serve as an important connection between participants, physician principal investigators, clinical research coordinators, and other members of the site team. For an RN moving from traditional bedside practice into clinical research, the position offers a way to retain meaningful clinical responsibilities while developing experience with study operations, participant safety, regulatory processes, and pharmaceutical-sponsored research in an urban clinical trial setting.

What to Consider Before Applying for This Clinical Research Nurse Role

Candidates considering this New York City Clinical Research Nurse position should be comfortable working in a structured, protocol-driven environment where consistency and documentation are as important as hands-on nursing skills. The role is based on-site and requires the ability to work between Adams Clinical locations in Harlem and the Bronx, so candidates should consider the practical demands of a dual-site position before applying. The work may be a strong fit for an RN who enjoys focused patient interactions, procedural nursing, careful review of clinical information, and collaboration with investigators and research coordinators rather than the faster pace and broader patient turnover commonly associated with hospital units. It can also suit nurses who want to build research experience without moving completely away from clinical practice. Because study procedures are governed by protocols and Good Clinical Practice requirements, attention to detail, reliable documentation, clear communication, and the ability to follow defined processes are important parts of the working environment. The position may be particularly relevant to nurses interested in developing longer-term experience in clinical research, trial operations, participant safety, or research-site nursing while remaining closely connected to patient-facing clinical work.

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