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About the Role

As a member of our clinical team, you will work under the supervision of our physician principal investigators and clinical nurse manager on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines. You will provide mentoring, direction, and guidance to clinical research coordinators and facilitate the informed consent process, administer screening procedures, perform data entry, and maintain regulatory binders.

Responsibilities

IV placement, initiation and management of IV infusions per sponsor provided protocol
Assist with difficult phlebotomy and IV placement for phlebotomy
Administration of subcutaneous or intramuscular injections
Medical record review
Assist with collection of AEs, concomitant medications, medical history
Timely reporting of Serious Adverse Events and follow up
Medical support on site for emergency situations
Willingness to commute to two locations in New York City area
Uphold GCP

Requirements

Registered Nurse license in New York State required
Bachelor’s degree in nursing required
2+ years of experience as a nurse preferred
Previous clinical research experience preferred, but not required
Willingness and ability to travel to both New York City office locations
Recent bedside experience

Skills

IV catheterization
Drug infusion
Injections
Phlebotomy
Medical record review
Lab results review
Medication reconciliation
Medical liaising
Informed consent process facilitation
Screening procedures administration
Data entry
Regulatory binder maintenance
Nursing functions

Location

New York City area

Work Type

Full-time

Experience Level

2+ years of experience as a nurse preferred

Education Level

Bachelor’s degree in nursing required

Salary/Compensations

$90K-110K annual salary, commensurate with experience

Benefits

401(k) matching
Medical, Dental & Vision insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Professional development assistance

About the Company

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines.
Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare.
Our vision is to set the gold standard for clinical trial excellence.
We believe our people make the difference.
Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.
At Adams Clinical, you’ll find: A culture of respect, transparency, and continuous improvement, Opportunities for professional growth and learning, A team dedicated to improving lives through innovation and integrity.

Equal Opportunity

Adams Clinical is committed to being an equal opportunity and affirmative action employer.
We focus on hiring and nurturing top talent.
All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate’s or employee’s qualifications relevant to the position.
These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.
In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required time frame.
Adams Clinical participates in E-Verify to confirm employment eligibility.