University of Chicago
Clinical Research Coordinator I
University of Chicago, Chicago, Illinois, United States, 60601
Clinical Research Coordinator I
The position is a Clinical Research Coordinator I (CRCI) for POH and other clinical research studies. The Clinical Research Coordinator I (CRCI) is an entry level researcher working with the Principal Investigator (PI) Dr. David Meltzer, Co-Investigator(s) and other study personnel, to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study. In addition to CRC1, the position will also serve as a Dental Assistant (DA1) at The University of Chicago Medicine (UCM) Dental Research Study Clinic and will be responsible for chairside assisting to dental providers providing dental care to patients at the University of Chicago Medicine (UCM) Dental Research Study Clinic at its main campus in Hyde Park as well as other study sites, including mobile dental units. Responsibilities include: Supports, facilitates and coordinates daily study activities while working with investigators and other staff. Educates patients about study procedures to be performed, the study visit schedule, what to report between and during visits, and the risks and benefits of the procedures. Plans and coordinates the schedule for study non-clinical visits and activities. With guidance from study protocols, investigators, and staff, conducts screening and informed consent for potential study enrollees, administer study questionnaires/surveys with study enrollees, collect intraoral images of study enrollees. Protects patients and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols. Prepares for or participate in quality assurance audits under supervision or following specific protocol procedures. Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. Recruit participants for other clinical research studies. Provides services at UCM Dental Research Study Clinic as well as affiliated study sites including mobile dental units across Chicagoland area. Helps patients feel comfortable before, during, and after dental treatment. Prepares patient for dental treatment by welcoming, comforting, seating, and draping patient. Schedules clinical appointments with patients in person and over the phone. Asks about the patient's medical history, blood pressure, and pulse. Documents measurements and treatments in the electronic dental record. Positions and passes instruments for dentist's access. Suctions patient saliva and debris during treatments. Maintains patient confidence by keeping information confidential. Provides patients with instructions for oral self-care following dental treatments. Teaches patients appropriate oral hygiene strategies to maintain oral health; (e.g., tooth brushing, flossing and nutritional counseling). Provides information to patients and employees by answering questions and requests. Prepares treatment room for patient by following prescribed procedures and protocols. Adheres to infection control and sterilization procedures and prepare instruments and equipment. Provides instrumentation by working with Central Sterile Processing to sterilize and deliver instruments to treatment area. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Maintains dental supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies. Accountable for all tasks in basic clinical studies. Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples. Performs other related work as needed. Minimum qualifications include a college or university degree in a related field and less than 2 years of work experience in a related job discipline. Preferred qualifications include a bachelor's degree and knowledge of medical terminology/environment. Preferred competencies include the ability to work independently and as part of a team, commitment to providing a high level of service and high degree of professionalism, attention to detail, excellent interpersonal, verbal, and written communication skills, ability to communicate with tact and diplomacy, ability to absorb large amounts of information quickly, and ability to handle multiple tasks simultaneously and under tight deadlines. Application documents required include a resume and cover letter. When applying, the documents MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
The position is a Clinical Research Coordinator I (CRCI) for POH and other clinical research studies. The Clinical Research Coordinator I (CRCI) is an entry level researcher working with the Principal Investigator (PI) Dr. David Meltzer, Co-Investigator(s) and other study personnel, to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study. In addition to CRC1, the position will also serve as a Dental Assistant (DA1) at The University of Chicago Medicine (UCM) Dental Research Study Clinic and will be responsible for chairside assisting to dental providers providing dental care to patients at the University of Chicago Medicine (UCM) Dental Research Study Clinic at its main campus in Hyde Park as well as other study sites, including mobile dental units. Responsibilities include: Supports, facilitates and coordinates daily study activities while working with investigators and other staff. Educates patients about study procedures to be performed, the study visit schedule, what to report between and during visits, and the risks and benefits of the procedures. Plans and coordinates the schedule for study non-clinical visits and activities. With guidance from study protocols, investigators, and staff, conducts screening and informed consent for potential study enrollees, administer study questionnaires/surveys with study enrollees, collect intraoral images of study enrollees. Protects patients and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols. Prepares for or participate in quality assurance audits under supervision or following specific protocol procedures. Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. Recruit participants for other clinical research studies. Provides services at UCM Dental Research Study Clinic as well as affiliated study sites including mobile dental units across Chicagoland area. Helps patients feel comfortable before, during, and after dental treatment. Prepares patient for dental treatment by welcoming, comforting, seating, and draping patient. Schedules clinical appointments with patients in person and over the phone. Asks about the patient's medical history, blood pressure, and pulse. Documents measurements and treatments in the electronic dental record. Positions and passes instruments for dentist's access. Suctions patient saliva and debris during treatments. Maintains patient confidence by keeping information confidential. Provides patients with instructions for oral self-care following dental treatments. Teaches patients appropriate oral hygiene strategies to maintain oral health; (e.g., tooth brushing, flossing and nutritional counseling). Provides information to patients and employees by answering questions and requests. Prepares treatment room for patient by following prescribed procedures and protocols. Adheres to infection control and sterilization procedures and prepare instruments and equipment. Provides instrumentation by working with Central Sterile Processing to sterilize and deliver instruments to treatment area. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Maintains dental supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies. Accountable for all tasks in basic clinical studies. Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples. Performs other related work as needed. Minimum qualifications include a college or university degree in a related field and less than 2 years of work experience in a related job discipline. Preferred qualifications include a bachelor's degree and knowledge of medical terminology/environment. Preferred competencies include the ability to work independently and as part of a team, commitment to providing a high level of service and high degree of professionalism, attention to detail, excellent interpersonal, verbal, and written communication skills, ability to communicate with tact and diplomacy, ability to absorb large amounts of information quickly, and ability to handle multiple tasks simultaneously and under tight deadlines. Application documents required include a resume and cover letter. When applying, the documents MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.