Clinical Research RN Position Available In Ontario, New York

Job Description:

Location Detail:

560 Hudson St HH E&R Ctr (10058)

ShiftDetail:

Monday-Friday Work where every moment matters. Every day,almost 30,000 Hartford HealthCare employees come to work with onething in common: Pride in what we do, knowing every moment mattershere. We invite you to become part of Connecticut’s mostcomprehensive healthcare network. The Hartford HealthCare CancerInstitute focuses on offering our cancer patients an unparallelednetwork of coordinated services- all under one roof. Our system ofcare includes a truly integrated team with the most talented,experienced, and compassionate caregivers and physicians, backed bythe latest cutting-edge technology. The Oncology Clinical ResearchNurse (RN) of Cancer Clinical Research Office (CCRO) is an integralmember of the research team. In compliance with all regulatory,institutional and departmental requirements, performs patientscreening, 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 appropriateconduct of clinical research trials in oncology which may besupported by the NCI, industry, cooperative groups or HHC systemalliances.
• Coordinate and conduct the operation of clinicaltrials as per GCP and ICH guidelines including participantrecruitment; informed consent; continuous monitoring of protocolfor compliance and patient safety; source document review; dataentry; sponsor monitoring.
• Interact/collaborate with allphysicians, other members of the health care team andparticipants/families across the system in a manner that supportsthe conduct of clinical trials.
• Required to attend the respectivesystem-wide Disease Management Team meetings and present theclinical trials to potential investigators.
• Collaborate with andsupport other clinical trial staff across the system to ensurehighest quality clinical research activities.
• Document relevantdata collections into various sponsor electronic data capturesystems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participanttracking logs and screening/enrollment logs.
• Assist regulatorystaff with study regulatory reporting requirements and IRB policiesfor protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trialbilling in the resolution of related queries.
• Assist/coordinatepreparation for internal and external audits.
• Handle allconfidential information appropriately.

QualificationsRequirements:

• Bachelor’s degree Nursing
• Minimum of 2-3 years ofrelevant clinical research experience.
• Demonstrated clinicalcompetency with patient related measurements and with a high degreeof accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity withdatabases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) andquerying.
• Experience with Microsoft Access, Excel and electronicdata capture systems.
• Experience in preparing and completing CaseReport Forms (CRF’s), eligibility checklist and other relevantdocumentation protocols.
• Excellent interpersonal skills arerequired for working with the study participants and working as amember of a highly integrated team.
• Ability to travel betweenclinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offersexciting opportunities for career development and growth. Here, youare part of an organization on the cutting edge – helping to bringnew technologies, breakthrough treatments and community educationto countless men, women and children. We know that a thrivingorganization starts with thriving employees we provide acompetitive benefits program designed to ensure work/life balance.

Every moment matters. And this is your moment .