Clinical Research Nurse Coordinator, Oncology Trials
Overview
You will coordinate oncology clinical trials at a major research institution, ensuring compliant study conduct and serving as the key liaison among investigators, nurses, and regulators. You will oversee study feasibility, regulatory submissions, patient recruitment, and documentation across multiple concurrent trials. Working onsite in Paramus, NJ, you will collaborate with principal investigators and a multidisciplinary team. This contract-to-hire role offers the chance to impact patient care and advance oncology research.
What You'll Do10
- 1Liaise between principal investigators, sub-investigators, and regulatory specialists on protocol changes and regulatory issues.
- 2Assess study feasibility and competition with existing protocols before submission.
- 3Prepare trial protocols and ensure departments receive documentation, including scientific merit and accrual potential.
- 4Submit protocol revisions, informed consents, continuing reviews, and serious adverse events to the IRB of record.
- 5Develop study budgets with investigators and finalize drafts with the budget coordinator.
- 6Recruit and evaluate potential study patients, coordinating appointments and interviews.
- 7Document patient medical histories and perform nursing assessments, tracking responses with toxicity flow sheets.
- 8Maintain accurate records in electronic medical records, clinical trial management systems, and study databases.
- 9Educate patients, caregivers, and staff on trial procedures, treatments, and side effects, including informed consent and HIPAA.
- 10Coordinate research activities, including labs, radiology, and specimen processing, and prepare for sponsor monitoring visits.
Requirements11
- 1Active RN license and BSN; advanced nursing degree may substitute.
- 23+ years clinical nursing experience, or 1 year nursing plus 2 years clinical research.
- 3Experience as a clinical research nurse or coordinator in oncology.
- 4Proficiency in IRB submissions, continuing reviews, and adverse event reporting.
- 5Skill in recruiting and screening patients for trial eligibility.
- 6Experience with electronic medical records and clinical trial management systems.
- 7Ability to develop and manage study budgets.
- 8Competence in performing EKGs and processing biological specimens.
- 9Knowledge of HIPAA and informed consent procedures.
- 10Strong organizational skills for managing multiple trials and deadlines.
- 11OCN credential or eligibility preferred.
Salary Insight
Salary not disclosed in listing
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