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...
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...
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...
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...
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...
Minimum 2 years of clinical research experience, preferably on a federally funded grant. 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 acti...
Senior Clinical Research Coordinator – Oxnard, CA. Senior Clinical Research Coordinator. Daily Responsibilities for Senior Clinical Research Coordinator:. Required Qualifications for Senior Clinical Research Coordinator:. ...
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...
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...
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 ...
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...
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,...
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. 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...
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;...
Participates in subject screening and schedules research study participants for study visits. ...
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, (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...
Clinical Research Coordinator (CRC) Assistant. The CRC assistant will support the CRC, administrative staff and principal investigators, assist the communications between sponsor and institute, oversee details of clinical studies and ensure compliance with study review board and clinical research re...
Identifies and explains the responsibilities of Principal Investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial. Recruits and interviews potential study patients with guidance from PI and other cl...
The Division ofGastroenterology and Hepatology is seeking an academic hourly Clinical ResearchCoordinator who will manage and coordinate the timely handling of allcomponents of clinical research protocols, including pre and post researchactivities, internal and external to the clinic setting. Certif...
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. ...
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...