A company is looking for a Clinical Research Coordinator for a Clinical Trials Processing Lab. ...
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. ...
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. ...
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...
CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. You support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout t...
Month Contract Clinical Research Coordinator role in Chicago, IL (60615). We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team and assist with vaccine trials. The ideal candidate will play a critical role in coordinating and overseeing the daily activities of...
Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit. Clinical Research Coordinator I. Assisting Clinical Research Coordinators with patient visits, documentation, CRF completion, data...
The Clinical Research Coordinator will oversee the day-to-day operations of biomedical and/or social-behavioral research studies, working with multidisciplinary teams, sponsors, and external stakeholders. Clinical Research Coordinator - Orland Park, IL (60462). The coordinator will also serve as a r...
Visiting Clinical Research Compliance Coordinator. The Office of Population Health Sciences (OPHS) at UIC is seeking applications for a Visiting Clinical Research Compliance Coordinator. Educate and guide OPHS Clinical Research Team in the design and conduct of human subject research to ensure compl...
Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholders. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all curren...
Occasionally attending out-of-town Investigator Meetings Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent Facilitate ef...
As a Clinical Research Coordinator, you will be at the forefront of managing daily operations of biomedical and/or social-behavioral research studies. Job Title: Clinical Research Coordinator. The team includes Clinical Research Managers, Project Managers, CRC Leads, CRCs, and Data Coordinators. You...
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 ...
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. High School Diploma with five to seven years clinical research experience -or- Associates/two years of College with four to six years clinical research experience or. Bachelors with three to ...
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 Clinical Research Coordinator manages and directs the coordination and timely handling of all components of clinical research protocols in Neurosurgery; including pre and post research activities, in and outside of the clinical setting. Knowledge of research protocols, principles and procedures;...
Provides complex scientific & technical leadership in determining research priorities & the plan, design & execution of research projects ensuring that programs of investigation meet specified objectives. Manages all activities associated with biomedical &/or social-behavioral resear...
Identify and explain the responsibilities of Principal Investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial. Understanding of the federal research regulations and the ability to identify the fede...
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 Pediatri...
The Clinical Research Coordinator, (CRC) is to screen, enroll and follow study subjects while ensuring protocol and regulatory compliance and close monitoring while subjects are in study. Four years of Clinical Research Coordinator experience. Maintain adherence to FDA regulations and ICH guidelines...
EKG, blood collection)Processing all samples and shipping to Central LabMaintaining study sourceEntering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working ...
We are seeking a full-time Clinical Research Coordinator with a minimum of 1 year of clinical research experience, for our Elgin, Il location. Clinical Research Coordinators here at Revival Research Institute , should be genuinely respectful...
Two years of experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice. Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinic...
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...
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. The Clinical Research Coordinator (CRC) is responsible for the coordination and administrati...