Job Schedule: Full Time Standard Hours: 40 Job Shift: Shift 1 Shift Details: M-F Normal business hrs (8am-5pm) with modifications based on patient care needs. Requires intermittent travel between our health system locations
where every moment
Every day, almost 25,000 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 as a Biospecimen
Clinical Research Coordinator l 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. This position specifically supports
non-therapeutic and biospecimen focused research and serves as a research
and facilitate the appropriate conduct of biospecimen studies in oncology.
therapeutic research through specimen collection, processing, shipping and
timed assessments. Coordinates with pathology and sponsors for tissue samples.
inventory management of research laboratory supplies.
protocols and laboratory manuals to assess for impact, logistical planning and
and conduct studies 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; processing, storing and shipping of
research specimens in accordance with study laboratory manual and IATA
with and support other clinical trial staff across the system to ensure highest
quality clinical research activities.
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
regulatory staff with study regulatory reporting requirements and IRB policies
for protocol deviations, safety reporting and continuing reviews.
research account specialist of CCRO with clinical trial billing in the
resolution of related queries.
preparation for internal and external audits.
Handle all confidential information appropriately.
duties as assigned.
Bachelor’s degree (in Nursing, Pharmacy, or Healthcare related).
of 2-3 years of relevant clinical research experience.
with basic laboratory principles and safe handling of blood and other biological
clinical competency with patient related measurements and with a high degree of
accuracy with respect to documentation and data collection.
to work with spreadsheets (such as Excel), familiarity with databases (ex:
RedCap, Medidata, RAVE, etc.) and querying.
in preparing and completing Case Report Forms (CRF’s), eligibility checklist
and other relevant documentation protocols.
interpersonal skills are required for working with the study participants and
working as a member of a highly integrated team.
to travel between clinical sites in the Greater Hartford area, whenever
We take great care of careers.
With locations around the state, Hartford HealthCare offers
exciting opportunities for career development and growth. Here, you are
part of an organization on the cutting edge – helping to bring new
technologies, breakthrough treatments and community education to countless men,
women and children. We know that a thriving organization starts with
thriving employees-- we provide a competitive benefits program designed to
ensure work/life balance. Every moment matters. And this is your