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|Date Posted||March 8, 2019|
Health Research Institute
|Address||2900 W Oklahoma Ave|
Supports research initiatives in a specific department or clinical area of Aurora Health Care. Assists the investigators, residents, students, scientists, healthcare providers, fellows, and other research staff in the planning of studies, conducting projects, and disseminating findings.
Assists the principle investigator(s) or Sr. Research Associate to design, develop, obtain Institutional Review Board (IRB) approval, implement and disseminate investigator initiated research. May participate in study participant recruitment and data and/or biospecimen collection activities. May interview and evaluate study participants to determine trial/project eligibility and disseminate information for enrollment on protocol once eligibility is confirmed. Assists in coordination of data analysis and manuscript writing.
May schedule study participants participating in research projects for tests and procedures according to protocol design and sets up qualification, initiation and monitoring visits throughout the study, as needed.
Assists in the review of subject medical records, database records and other sources to screen and identify potential subjects for inclusion in research projects based on criteria described in the protocol
Assists heath care professionals including various research staff in the conduct of projects in an ethical and safe manner according to Good Clinical Practice (GCP), standard operating protocols (SOPs), Institutional Review Board (IRB) policies and procedures, and regulatory standards.
Collection of biospecimens and/or data and completes and submits data on appropriate documents according to the IRB, the Clinical Research Department's Standard Operating Procedures (SOPs), or regulatory policies, including routine data reporting, submissions, continuing reviews, amendments and adverse event reporting.
We are looking for two Associates:
One of the two research associates will be working closely with the interventional cardiologist group, and the other will be working more closely with the CV surgeons and EP group.
Ideal candidate will have in clinical research, regulatory submissions, scientific publications, study design, etc.