Coordinates with the Clinical Research RN to organize procurement of research samples and then prepares, packages and ships research samples. CLINICAL RESEARCH COORDINATOR II. Collect and manage patient and laboratory data for clinical research projects. Collect and manage patient and laboratory dat...
This position is entirely an on-site CRC role requiring daily travel to a primary site.This role may periodically require travel to a secondary site to provide support or temporary coverage as needed....
Clinical Research Coordinator Opportunity in Chicago, IL(60611). Medix is currently seeking experienced Research Professionals wanting to grow their career in the Clinical Research Field. Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and f...
Manages clinical research studies and adheres to Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), study protocols, clinical trial agreements, and regulations governing clinical research. Our client is seeking a Clinical Research Coordinator to work onsite at their Chicago, IL lo...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as doc. ...
Research Coordinator, Clinical Research, Coordinator, Clinical, Healthcare, Education, Research. ...
Serves as an initial point of contact for clinical research participants and clinical staff, providing information regarding research procedures, expectations, and informational inquiries. Coordinates clinical research studies, performing related tasks and activities. Schedules logistics, determines...
The Clinical Research Coordinator manages and coordinates the timely handling of all components of clinical research protocols, including pre and post research activities, that are internal and external to the clinical setting. Knowledge of research protocols, principles and procedures; knowledge of...
High School Diploma with three to five years research experience -or- Associates /two years of College with two to four years research experience or- Bachelors with one to three years research experience. Coordinates study conduct with other departments to effectively implement clinical research pro...
Clinical Research Coordinator (CRC). The CRC will support principal investigators, work as a link between sponsor and institute, oversee details of clinical studies and ensure compliance with study review board and clinical research regulations. Clinical research certification. Working knowledge of ...
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Promotes the ethical conduct of research and Lurie Children’s by serving in a leadership/appointed role of an internal/external clinical research committee (e. High School Diploma with five t...
Provide support in training new coordinators to ensure seamless integration into the research team. Experience: Two years of clinical research experience working with adults who have aphasia or a related dementia syndrome. Location: Chicago, IL Job Description: Manage the recruitment and scheduling ...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...
Senior Clinical Research Coordinator – Oxnard, CA. Senior Clinical Research Coordinator. Daily Responsibilities for Senior Clinical Research Coordinator:. Required Qualifications for Senior Clinical Research Coordinator:. ...
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Promotes the ethical conduct of research and Lurie Children’s by serving in a leadership/appointed role of an internal/external clinical research committee (e. Coordinates all clinical resear...
Works in collaboration with Chief Integrity Officer and research leaders to develop and implement research compliance education and training programs for all research staff, including without limitation clinical research billing, research misconduct, human research protections, conflict of interest,...
Coordinates schedules and monitors research activities and subject preparation for minimal risk studies for a defined clinical research trial(s). Collects, abstracts, and enters research data. Experience working with patients and families in clinical settings preferred. ...
The Pediatric Clinical Trials Office (Peds CTO) is an existing centralized support office that provides services and high level guidance to individuals (faculty, investigators, research staff, and clinic coordinators from the University and Hospital) involved in human subjects research. The Clinical...
Coordinates schedules and monitors research activities and subject preparation for minimal risk studies for a defined clinical research trial(s). Collects, abstracts, and enters research data. Experience working with patients and families in clinical settings preferred. ...
Acts as a resource on clinical research and related aspects of clinical study for other clinical research staff. CRC) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the Section Administrator and/or Clinical Research Manager within the ...
Clinical Research Coordinators, Research Associates, Graduate Students, Students, Volunteers. The UIC Office of the Vice Chancellor for Health Affairs - Office of Population Health Sciences seeks Visiting Clinical Research Compliance Coordinator. The UIC Office of the Vice Chancellor for Health Affa...
Duration: 12 Months (Possibility of extension) Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operat...
Works under the general direction of a departmental, clinical research manager and/or the Office of Clinical Research (OCR) in partnership with the Principal Investigator (PI), Co-Investigator(s) and other study personnel. Coordinates, completes and monitors the daily clinical trial activities and p...
The Clinical Research Coordinator 1 works under the general direction of the PI and HAARC Center Clinical Research leadership. The Clinical Research Coordinator 1 (CRC1) provides support to the Healthy Aging & Alzheimer’s Research Care (HAARC) Center within the Biological Sciences Division. The Heal...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...