Clinical Research Nurse 1

Yale University; New Haven (CT); On-site; USD 65,000 - 85,000; Full time

Job summary

An esteemed university in Connecticut is seeking a dedicated clinical research coordinator. This role involves enrolling research subjects, providing clinical services, and ensuring compliance with protocols. Candidates should have a Bachelor's degree in Nursing and 3 years of relevant experience. Strong teamwork and communication skills are essential. The position offers an opportunity to contribute to impactful research while supporting diverse study staff.

Qualifications

• 3 years of related experience or an equivalent combination of education and experience.
• Ability to train staff on study protocols.
• Excellent oral and written communication skills.

Responsibilities

• Identifies, assesses eligibility, and enrolls research subjects.
• Provides direct clinical services and observes subjects.
• Contributes to protocol development and regulatory compliance.
• Conducts evaluations and administers medications.

Skills

Teamwork and leadership

Communication skills

Phlebotomy

Critical thinking

Education

Bachelor’s of Science Degree in Nursing

Job description

Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!

Overview

Identifies, assesses eligibility, enrolls, and collects accurate medical and demographic history on research subjects for a variety of studies; obtains and explains written consent for subject participation. Provides direct clinical services to subjects; observes subjects and notifies clinicians to any medical/emotional change. Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes. Conducts patient and research subject evaluations; administers medications and research instruments, and presents data. Reviews, codes and contributes in the entering of all collected patient data to assure completeness and accuracy. Ensures regulatory compliance by maintaining clinical and nursing records to meet the needs of various protocols. Maintains the integrity of the clinical research study by striving to advocate for patients. May perform other duties as assigned.

Required Skills And Abilities

• Teamwork and leadership: Ability to work constructively toward a team goal and leads a group of diverse study staff.
• Ability to train staff on study protocols and determine the appropriate level of independence to provide to staff.
• Ability to monitor for, identify, think critically about and propose/implement solutions for inefficiencies and errors.
• Excellent oral and written communication skills. Protocol implementation.
• Proven ability with Phlebotomy and placement of peripheral IV lines.

Principal Responsibilities

• Identifies, assesses eligibility, enrolls, and collects accurate medical and demographic history on research subjects for a variety of studies; obtains and explains written consent for subject participation.
• Provides direct clinical services to subjects; observes subjects and notifies clinicians to any medical/emotional change.
• Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes.
• Conducts patient and research subject evaluations; administers medications and research instruments, and presents data.
• Reviews, codes and contributes in the entering of all collected patient data to assure completeness and accuracy.
• Ensures regulatory compliance by maintaining clinical and nursing records to meet the needs of various protocols.
• Maintains the integrity of the clinical research study by striving to advocate for patients.
• May perform other duties as assigned.

Required Education and Experience: Bachelor’s of Science Degree in Nursing and three years of related experience or an equivalent combination of education and experience.

EEO Statement

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). Yale University is a tobacco‑free campus.