Clinical Research Nurse
1 month ago
Responsibilities:
- Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
- Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
- Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
- Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
- Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
- Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
- Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
- Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
- Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
- Assist/coordinate preparation for internal and external audits.
- Handle all confidential information appropriately.
Qualifications
- Bachelor’s degree Nursing
- Minimum of 2-3 years of relevant clinical research experience.
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