Clinical Research Nurse- 226044
2 weeks ago
Responsibilities:
- Organize and facilitate the smooth execution of clinical research trials in oncology, whether funded by the industry, cooperative groups, or system alliances.
- Manage and oversee the implementation of clinical trials in adherence to GCP and ICH guidelines, including tasks such as participant recruitment, obtaining informed consent, continuous protocol monitoring for compliance and patient safety, reviewing source documents, data entry, and sponsor monitoring.
- Collaborate closely with physicians, healthcare team members, and participants/families across the system to ensure seamless execution of clinical trials.
- Attend Disease Management Team meetings and present clinical trials to potential investigators within the system.
- Work collaboratively with other clinical trial staff across the system to maintain the highest standards of clinical research.
- Record pertinent data into various sponsor electronic data capture systems and complete data entry within specified protocol timelines.
- Develop study calendars and materials, maintain participant tracking logs, and manage screening/enrollment logs.
- Assist regulatory staff in meeting study regulatory reporting requirements and adhering to IRB policies regarding protocol deviations, safety reporting, and continuing reviews.
- Support research account specialists in resolving clinical trial billing queries.
- Assist in coordinating internal and external audits.
- Maintain confidentiality of all relevant information.
Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
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