Clinical Research RN

Work where every

moment

matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common : Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut's most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

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