Clinical Research Coordinator
3 weeks ago
Description
Job Schedule: Full TimeStandard Hours: 40
Job Shift: Shift 1
Shift Details: Flexibility is required to accommodate subject schedules and study activity. Some weekends and off-hours possible.
Workwhere every momentmatters.
Every day, over 30,000 Hartford HealthCare colleagues come to work with onething in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcarenetwork as a Visiting Registered Nurse.
St. Vincent’s Medical Center is thefirst hospital in Fairfield County to be integrated into the HartfordHealthCare network, and is the system’s second-largest hospital. Located in Bridgeport, St. Vincent’s has morethan 3,200 employees and includes a 473-bed community hospital, a 76-bedinpatient psychiatric facility in Westport and special needs services foradults and children.
The Clinical Research Coordinator willwork in the Connecticut Orthopaedic Institute at St. Vincent’s MedicalCenter. In compliance with allregulatory, institutional, and departmental requirements, the Clinical ResearchCoordinator is responsible for clinical research and trial design, patientscreening, data collection and entry, and ensuring data quality and integrityin the implementation of research protocols.
Job Description- Oversees management andoperation of clinical protocols to ensure research participant accrual,research participant safety, data quality and protocol compliance.
- Interacts with physicians,health care team members and trial participants/family members in a manner thatsupports the conduction of clinical trials.
- Utilizes Clinical TrialManagement Systems (CTMS) and various databases (Access, Excel, RAVE, iRIS,etc.) and source records in electronic medical record systems to collectresearch participant information.
- Manages protocol calendars,schemas, schedules and participant tracking logs; schedules patient visits forvarious study related procedures.
- Develops standard operatingprocedures to ensure highest quality research operations.
Qualifications
Qualifications- Bachelor’s degree (Nursing,pharmacy, or healthcare related)
- 2-5 years of relevantclinical research experience, conducting orthopedic clinical trials or clinicalresearch experience within the orthopedic field. Any appropriate combination of relevanteducation, experience and/or certifications may be considered.
- Experience in preparing andcompleting Clinical Research Forms (CRF), Informed Consent Forms (ICF),Standard Operating Procedures (SOPs), Institutional Review Board (IRB)submissions, eligibility checklists and other protocol relevant documentationprotocols.
- Proficiency with MicrosoftAccess, Excel and electronic data capture systems.
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