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Clinical Research Nurse
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Hackensack, New Jersey, United States Incredible Health Full time{"h2": "Clinical Research Nurse Position at Incredible Health ", "ul": ["\u2022\u00a0\u00a0We are actively hiring for a Clinical Research Nurse at our Hackensack, NJ location. \u2022\u00a0\u00a0As a Clinical Research Nurse, you will work closely with Principal Investigators and other healthcare professionals to coordinate and manage patient care in line with...
Oncology Clinical Research Nurse
2 months ago
At HealthEcareers - Client, we're committed to delivering exceptional patient care and advancing the field of oncology through innovative clinical research. As an Oncology Clinical Research Nurse in our Solid Division, you'll play a vital role in coordinating and overseeing clinical operations of clinical trials, ensuring the highest standards of patient care and compliance.
Key Responsibilities- Protocol Management: Assist the principal investigator in preparing proposed clinical trials, reviewing trial protocols, and ensuring timely submission of protocol revisions, informed consents, and continuing reviews to the IRB of record.
- Regulatory Compliance: Act as liaison between principal investigators and sub-investigators on all regulatory issues and changes within the protocol, interacting with regulatory specialists and principal investigators to ensure compliance.
- Patient Recruitment and Education: Recruit and evaluate potential study patients, work with clinical research coordinators to schedule appointments and interviews, and educate patients on clinical trials, treatments, and side effects.
- Medical Record Management: Review medical records for potential study patients, ensure documentation of laboratory test results and procedures, and maintain accurate, complete, and up-to-date records on each patient participating in a clinical trial protocol.
- Communication and Collaboration: Coordinate research activities, notify principal investigators of adverse events and serious adverse events, and report all serious adverse events to the sponsor and IRB of record according to established timelines.
To succeed in this role, you'll need to possess excellent communication and organizational skills, a strong understanding of clinical research principles, and the ability to work collaboratively with cross-functional teams. If you're passionate about advancing oncology research and delivering exceptional patient care, we encourage you to apply.
