Clinical Research Nurse 2

Yale Cancer Center; New Haven (CT); On-site; USD 68,000 - 121,000; Full time

Job summary

Yale Cancer Center is seeking a Clinical Research Nurse II to support patients in clinical trials within the Clinical Trials Office. The role emphasizes compliant, efficient conduct of trials and patient safety.

Responsibilities include coordinating trial activities, ensuring protocol adherence, obtaining informed consent, and providing patient education, with a focus on regulatory compliance and collaboration with investigators.

Qualifications

• Graduate of an accredited nursing program with at least 3 years of nursing experience in hospital, clinic, or similar health care setting, or 3 years of clinical research nurse experience.
• Connecticut RN licensure or license eligible.
• Experience with clinical trials and adherence to protocol, ICH/GCP, and regulatory requirements.

Responsibilities

• Coordinates, implements, and evaluates all aspects of clinical trial conduct for moderately to highly complex protocols.
• Assists study feasibility reviews and recruitment of participants.
• Adheres to study protocol, maintains documentation, and ensures regulatory and sponsor requirements are met.
• Identifies noncompliance and deviations and reports them to appropriate parties.
• Develops training materials and protocol-specific tool kits for training.
• Performs direct patient care including ECGs and administration of research instruments per protocol.

Skills

Clinical research nursing

Informed consent

Regulatory compliance

Microsoft Office

Communication skills

Education

Nursing degree from accredited program

Tools

CTMS

Job description

Overview

The Clinical Research Nurse II (CRN II) is responsible for providing research services to patients participating in clinical trials within the Yale Cancer Center Clinical Trials Office, while ensuring safe, compliant, efficient, and effective conduct of clinical trials.

Required Skills and Abilities

• 1. Excellent clinical, analytical, and organizational skills with demonstrated research nursing ability. Proven ability to draft, proofread, and document items that are complex in nature. Proven ability to be meticulous with details. Strong computer skills required, including strong competency in Microsoft Office programs (Word, Excel, PowerPoint, etc.).


• 2. Proven ability to multi-task, maintain confidentiality and remain focused in a fast-paced environment. Excellent time management and organizational skills.


• 3. Proven ability to interpret complex protocols and evaluate and assess subject’s suitability for inclusion into studies, obtain informed consent, determine patient eligibility, and coordinate patient enrollment.


• 4. Proven ability to coordinate patient care. Strong interpersonal skills with the proven ability to communicate effectively.


• 5. Knowledge of Food and Drug Administration (FDA) regulations, Good Clinical Practice (GCP) guidelines, and other applicable federal regulations.

Preferred Skills and Abilities

• 1. Proven experience in oncology research setting and experience working with Federal Regulations and IRBs is preferred.


• 2. Minimum two (2) years of clinical research nursing experience strongly preferred.


• 3. Knowledge of Clinical Trials Management Systems (CTMS).

Preferred Licenses or Certifications

• ACRP/SOCRA (or equivalent) certification preferred.


• ONS certification

Principal Responsibilities

• 1. Coordinates, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administration for moderately to highly complex protocols.


• 2. Assists study feasibility reviews.


• 3. Adheres to study protocol, maintains accurate documentation, recruits study participants, and ensures regulatory and protocol requirements and guidelines are met per ICH/GCP, federal regulation, and institutional and sponsor requirements.


• 4. Identifies instances of noncompliance and deviations from protocol and reports noncompliance and deviations to the appropriate parties.


• 5. Builds, reviews, and approves accurate and complete order sets to ensure compliance with individual research protocols. Reviews Beacon order set with CRC in anticipation of upcoming participant’s clinic visit. Pends orders for routing to Investigator for approval and signature.


• 6. Assists in ensuring Principal Investigator oversight by providing updates on protocol issues, obtaining signatures and clinical significance on lab reports, ECGs, adverse events, and other documents as required.


• 7. Develops and participates in the delivery of training for new protocols, including the creation of training materials, protocol-specific tool kit, nursing in-service presentations and others as required by specific protocols. Determines the appropriate training delivery mechanism, timing, and frequency.


• 8. Performs direct patient care (clinical and non‑clinical assessments) including, but not limited to electrocardiograms and administration of research instruments per study protocol requirements.


• 9. Maintains the integrity of the clinical research study by striving to advocate for patients and families. Serves as clinical resource for triaging and addressing research related inquiries generated from YCC websites and professional presentations.


• 10. Provides patient education and medical information to study participants and families to ensure understanding of proper medication dosage, administration, and side effects, when appropriate.


• 11. Serves as front line medical person in interpreting protocol to medical and nursing staff, particularly concerning dose medications and safety issues related to the administration of the study drug or treatment.


• 12. Participates in monitoring visits, and external audits (e.g., sponsor, FDA) to ensure smooth and positive process and outcome.


• 13. Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.


• 14. Performs other duties as assigned.

Required Education and Experience

Graduate of an accredited nursing program and minimum three (3) years of related nursing experience in a hospital, clinic, or similar health care setting required or 3 years of clinical research nurse experience, or equivalent combined experience, or the equivalent combination of education or experience. Experience must indicate the ability to work with minimal supervision in a team environment.

Required License(s) or Certification(s)

Licensure as Registered Nurse in the State of Connecticut or Connecticut license eligible.

Job Posting Date

08/07/2026

Job Category

Professional

Bargaining Unit

NON

Compensation Grade

Administration & Operations

Compensation Grade Profile

Manager; Program Leader (P5)

Salary Range

$68,000.00 - $120,500.00

Time Type

Full time

Duration Type

Staff

Work Model

Hybrid

Background Check Requirements

All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks basedon the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.

Health Requirements

This role is a healthcare worker position. Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.

Posting Disclaimer

Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and current internal and external market conditions.

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties throughtheir hiring department.

The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.

Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.