Clinical Trials Nurse – Day Shift (Ob/Gyn)

Vanderbilt Health; Nashville (TN); On-site; USD 70,000 - 105,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Tuition reimbursement

Retirement plan

Job summary

Vanderbilt Health in Nashville, TN, seeks a Research Nurse (Clinical Trials) to protect the integrity and quality of clinical research trials while supporting participants and study teams. With guidance from leadership, you will coordinate recruitment and enrollment activities and ensure strict adherence to study protocols and regulatory requirements.

Under supervision, you will manage study visits, document data accurately, and communicate with investigators and sponsors to support trial

Qualifications

• Bachelor’s degree or equivalent relevant experience.
• Active Tennessee Registered Nurse license.
• 2+ years of clinical trials experience strongly desired.
• Ob‑Gyncology experience is a plus.
• Experience with Workday and eStar is a plus.

Responsibilities

• Conveys understanding of policies, procedures, and regulations governing human subject research and applies them in care of participants.
• Assist with new research proposals, amendments, continuing reviews and adverse events.
• Perform administrative duties for trials: procuring equipment, documentation, packaging and shipping medications.
• Utilize nursing skills to deliver individualized care and follow research protocols.
• Recruit and assess candidate eligibility and monitor continued eligibility for participation.
• Engage in ongoing training and development to enhance professional performance.
• Responsibilities may include additional duties as assigned.

Skills

Nursing

Clinical Trials

Regulatory Compliance

Participant Recruitment

Study Coordination

Education

Bachelor’s degree

Tools

Workday

eStar

Job description

Vanderbilt Health in Nashville, TN, seeks a Research Nurse (Clinical Trials) to protect the integrity and quality of clinical research trials while supporting participants and study teams. With guidance from leadership, you will coordinate recruitment and enrollment activities and ensure strict adherence to study protocols and regulatory requirements.

Under supervision, you will manage study visits, document data accurately, and communicate with investigators and sponsors to support trial