In this role, you will provide as an integral member of the clinical research team to research study participants direct nursing care, patient and study assessments, education and patient/ family support.
The Clinical Coordinator will be responsible for establishing and maintaining a therapeutic relationship with patients and their families, as well as serving as a liaison between the physician and the patient and their family for home and hospice care.
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 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, the selected candidate will demonstratedoral and written communication and computer/database management skills; assist the Program Lead and study team with the scientific conduct of clinical studies.
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 Clinical Coordinator is responsible for implementing the clinical programs including individual, group, and family therapy services and carrying out administrative duties related to clinical program which includes clinical progress notes, treatment planning, psychological reports, utilization review forms, and discharge planning.
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, the selected candidate will explain the necessity, preparation, nature and anticipated effects of scheduled research procedures to the subject/patient; work cooperatively and assists other clinical staff to accurately and consistently complete study assignments.
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.