Clinical Research Coordinator II - Biospecimen

Location Detail: 560 Hudson St HH E&R Ctr (10058) Shift Detail: Monday-Friday Work where every moment matters. Every day, more than 40,000 Hartford HealthCare colleagues 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 Clinical Research Coordinator I of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements it performs patient screening, consent, data collection and data entry for research protocols, and projects within Hartford Healthcare Cancer Institute. This position specifically supports studies that involve collection of biospecimens such as blood and leftover surgical tissue. Position Responsibilities Coordinate and facilitate the appropriate conduct of biospecimen studies in oncology: screening and consenting patients, collecting blood and other specimens from study patients. Work with clinical trial coordinators on research specimen collection, processing, shipping and timed assessments. Coordinate with pathology and study sponsors for submission of archived surgical tissue samples. Review cancer clinical trial protocols and laboratory manuals for logistical planning and training needs. Conduct studies in accordance with federal regulation and guidelines governing clinical research including informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring; processing, storing and shipping of research specimens in accordance with study laboratory manual and IATA regulations. 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. Perform research blood draws as needed. 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. Provide inventory management of research laboratory supplies. Qualifications Education Bachelor’s degree (in Nursing, Pharmacy, or Healthcare related). Experience Minimum of 2 years of relevant clinical research experience. Familiar with basic laboratory principles and safe handling of blood and other biological specimens. Knowledge, Skills and Ability Requirements Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection. Review patient medical charts – familiar with Epic or other electronic medical record. Phlebotomy trained or willing to train. Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: RedCap, Medidata, RAVE, etc.) and querying. Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant clinical research documentation. Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team. Ability to travel between clinical sites in the Greater Hartford area, whenever required. #J-18808-Ljbffr Hartford HealthCare