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.
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..
The Research Coordinator is an entry-level role for candidates with research experience and who have a bachelors degree in behavioral or quantitative social sciences or a related subject. You will work as part of a team responsible for delivering insights and ad effectiveness measurement.
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 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.
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 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 assisting the clinical research team in overall study coordination, including, but not limited to, preparing for study initiation and activation, acquisition of source documents, record maintenance, preparing study documents, patient registration, coordinating and data entry.