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https://illinoisjoblink.illinois.gov/jobs/12666409 Department
BSD MED - Cardiology - Johnson Research Staff
About the Department
The Section of Cardiology was founded in 1950 and has a proud history.
We are now charting a new course that will propel us to the forefront of
cardiovascular medicine. The strength of the Section reflects the
quality and dedication of its faculty, trainees and support staff and is
enhanced by the rich environment at the University of Chicago.
Job Summary
This position conducts research according to study protocols that
investigate lifestyle and behavioral health interventions for adults
with chronic diseases. Under the direction of the Principal Investigator
(PI) or designee, the Clinical Research Assistant is responsible for
independently performing delegated tasks and procedures involving human
subject research. This work includes medical chart reviewing, patient
screening and consenting, coordination of regulatory activities,
intervention fidelity monitoring, and collection and management of data
for behavioral intervention study protocols related to cardiovascular
disease management. This is not a remote work position.
Responsibilities
Assist with the development, implementation, and refinement of
research processes and procedures as well as data collection
processes.
Obtain consent of research participants in accordance with the IRB
approved protocols and all applicable regulations including HIPAA.
Assist with recruiting, screening, selecting, maintaining and
terminating study subjects for multiple protocols.
Schedule and conduct participant study visits, tests and/or
interviews/telephone follow up calls.
Ensure accuracy and completion of all regulatory documentation,
including local or central IRB and study data. Provide data/support
to study Investigators, sponsors and/or external monitors/auditors.
Extract data from complex medical records with expert accuracy.
Assist with financial /operational aspects of grant and contracts.
Direct the activities of research support staff. Assist with the
training of staff.
Present study status reports related to assigned research projects.
Track and maintain study related information in the data management
system within the required timeframe.
Contribute to the design, development, and documentation of study
related data and collection tools, (e.g., questionnaires, treatment
data and/or therapeutic checklists).
Responsible for monitoring the inventory of research related
supplies.
Responsible for ordering project materials and supplies.
Document and collect data/ samples for research related procedures
performed during participant study visits. Ensure clinicians and/or
PI accurately document their study activities according to protocol.
Monitor strict adherence to all study protocols, including all
regulatory requirements adhering to appropriate federal, local and
institutional guidelines. Identify and resolve issues with protocol
compliance. Keep principal investigator and manager aware of any
issues regarding compliance.
Comply with all safety and infection control standards appropriate
to this position.
Adhere to Good Clinical Practice (GCP) guidelines and all human
subject protection practices Perform other duties as required.
Create systems for project implementation and data collection,
including source documentation.
Maintains system to provide patient compensation and schedule
transportation for participants.
Participate in required clinical research education and training
programs.
Assist with the preparation of research team meetings (meeting
agenda, minutes, etc.).
Performsall tasks in basic clinical studies.
Assists with and performs various administrative and operational
tasks as assigned under direct supervision.
Acquires and applies knowledge of clinical studies to collect
analyzable clinical research data and/or samples.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include vocational training, apprenticeships or the
equivalent experience in related field (not typically required to have a
four-year degree).
Work Experience:
Minimum requirements include knowledge and skills developed through
Certifications:
Preferred Qualifications
Education:
Master\'s degree in a scientific or health related field, or
equivalent experience.
Experience:
Experience using EPIC and REDCap.
Preferred Competencies
Ability to interact and communicate with clarity, tact, and courtesy
with patrons, patients, staff, faculty, students, and others.
Ability to communicat
