In this role, you will be responsible for
meet with investigators to discuss submission of proposals; prepare applications for IRB proposals; determine where supports are needed with regard to grants / budgets.
The Research Coordinator will manage and oversee research project activities ensuring adequate recruitment, data collection quality and integrity, and full compliance with all regulatory guidelines. Manages professional and support staff, reviewing work product to ensure study protocol is followed as written and approved by the relevant IRB..
In this role, you will assists research investigators in budgeting and managing financial accounts effectively within the guidelines and policies established by the Hospital as well as sponsoring agencies.
In this role, you will be responsible for the oversight/monitoring of all clinical trial expenses; reviews the protocol plan to differentiate standard of care versus research to ensure that clinical care expenses, personnel effort, site initiation costs, IRB fees, pharmacy costs, equipment, and supplies are tracked and captured as direct costs to the clinical trial.
In this role, you will coordinate recruitment, participant enrollment, and clinical services. Assesses patient eligibility for inclusion in clinical trials (may be multiple or various PIs). Ensures proper consent protocols have been followed for study participation.
In this role, you will be responsible for recruiting, consenting and interviewing post-Acute Coronary Syndrome patients and/or stroke patients in both the Emergency Department and inpatient settings; administering standardized questionnaires - some with potentially sensitive questions about mood; conducting follow-up interviews or sub-study visits on-site or in the community.
In this role, you will be responsible for coordination of a designated study or group of studies. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data.
The Research Coordinator will assist with day to day operations of CDC and CDPH funded projects that involve providing social service support to individuals living with or at risk for HIV/STIs in South Chicago.
In this role, you will be responsible to plans and organizes data collection activities in the cutaneous oncology center/mohs surgery division of facial plastics. Manages databases. Assists in the preparation of study designs, grants and manuscripts as well as irb submissions which may include literature searches and bibliography constructions.
In this role, you will coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research.
The position will be the lead coordinator for all neuro-oncology and gynecologic oncology trials. This position is also responsible for providing regulatory support for pediatric hematology/oncology and special projects as assigned.