Oncology Clinical Research Nurse Coordinator
Actalent
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Benefits offered by this job
Job summary
Actalent in Paramus, NJ is seeking a Clinical Research Nurse Coordinator to oversee oncology trial operations, ensure compliant conduct, and act as liaison among investigators, clinical staff, and regulatory specialists.
The role includes supporting feasibility, regulatory submissions, patient recruitment, informed consent, budgeting, and accurate documentation across EMR/CTMS; requires RN license, BSN, and oncology trial experience.
(This paragraph is a placeholder to maintain length)Qualifications
- Active RN license and clinical nursing experience.
- BSN required; MSN may satisfy BSN.
- Minimum 3 years clinical nursing, or 1 year clinical with 2 years research.
- Experience in oncology clinical trials and regulatory processes.
Responsibilities
- Coordinate regulatory submissions and IRB communications.
- Assist investigators in trial protocol reviews and budgets.
- Recruit and educate patients; schedule visits.
- Monitor patient safety and document adverse events.
- Maintain trial records across EMR and CTMS.
- Ensure compliance with HIPAA and protocol requirements.
Skills
Education
Tools
Job description
Actalent in Paramus, NJ is seeking a Clinical Research Nurse Coordinator to oversee oncology trial operations, ensure compliant conduct, and act as liaison among investigators, clinical staff, and regulatory specialists.
The role includes supporting feasibility, regulatory submissions, patient recruitment, informed consent, budgeting, and accurate documentation across EMR/CTMS; requires RN license, BSN, and oncology trial experience.
(This paragraph is a placeholder to maintain length)
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