About the role
About the Role
Under the direction of the Principal Investigator, the Research Nurse Specialist II (RNS II) plays a critical role in the successful execution of oncology clinical trials. This position ensures the integrity, quality, and compliance of clinical research studies while delivering high-quality, patient-centered care.
You will be responsible for managing patients throughout the full clinical trial lifecycle—from screening and enrollment through study completion—while ensuring adherence to protocols, regulatory guidelines, and Good Clinical Practice (GCP).
Key Responsibilities
- Manage clinical trial patients from screening → enrollment → study completion
- Implement and optimize patient recruitment strategies
- Ensure compliance with GCP, federal regulations, and sponsor protocols
- Perform study-related clinical procedures per protocol
- Maintain accurate, timely documentation and regulatory records
- Monitor and report adverse events and protocol deviations
- Collaborate closely with Principal Investigators, sponsors, and research teams
- Communicate effectively with patients, families, and cross-functional teams
Qualifications
- Registered Nurse (RN) required
- 3+ years of nursing experience
- At least 1 year of oncology experience (required)
- Clinical research experience preferred (not required)
- Strong understanding of clinical trials, compliance, and patient care
- Excellent organizational, communication, and multitasking skills
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