Job Description
Overview
We are seeking a dedicated Clinical Research Nurse to support oncology clinical trials in a patient-facing research environment. This role plays a critical part in coordinating study activities, ensuring protocol compliance, and providing education and support to study participants throughout the research lifecycle.
Key Responsibilities
- Coordinate and manage patient participation in clinical research studies, including recruitment, screening, enrollment, treatment administration, and follow-up in accordance with study protocols.
- Educate participants on study procedures, expectations, and responsibilities to ensure informed and compliant participation.
- Obtain, document, and maintain informed consent and HIPAA authorization, ensuring accuracy and ongoing compliance.
- Review study protocols and eligibility criteria with investigators and participants.
- Prepare, complete, and submit study documentation and case report forms within required timelines.
- Maintain accurate and complete source documentation, including clinical data, visit notes, and participant outcomes.
- Evaluate new and returning patients, review diagnostic imaging or scan results, and track eligibility and study status.
- Provide ongoing oversight of participants to ensure subject safety, protocol adherence, and data quality.
- Verify required approvals prior to treatment initiation or medication changes, including protocol-mandated dose adjustments or crossover.
- Dispense oral investigational products and educate participants on proper administration.
- Perform and document protocol-required clinical calculations (e.g., BSA, creatinine clearance, urine protein-to-creatinine ratios).
- Coordinate and schedule study visits, labs, imaging, and other protocol-required procedures.
- Identify, document, and report adverse events and safety findings per protocol and regulatory requirements.
- Complete study discontinuation documentation when applicable.
- Facilitate participant re-consent when updated informed consent forms are issued.
- Maintain investigational product accountability, including inventory management and reconciliation.
- Collaborate closely with investigators and research staff to meet study goals and timelines.
- Serve as a primary liaison between study participants, investigators, and the research team.
- Provide coverage or support at additional research sites as needed.
Required Qualifications
- Active RN license
- Associate’s Degree in Nursing
- Minimum 1 year of oncology experience
- 2 years of clinical research experience
Schedule
- Monday–Friday, 8:00 AM–5:00 PM
- Flexibility available based on patient visit schedules
Why Join Us?
- Growing research team with opportunities for upward mobility
- Hands-on involvement in meaningful oncology clinical trials
- Collaborative, patient-centered research environment
Job Tags
Monday to Friday,