Coordinates with the Clinical Research RN to organize procurement of research samples and then prepares, packages and ships research samples. CLINICAL RESEARCH COORDINATOR I. Collect and manage patient and laboratory data for clinical research projects. Serve as primary contact with research partici...
Serves as Primary Research Coordinator on studies across multiple sites guiding research team members involved in the study and coordinates and tracks research activities across sites. Senior Clinical Research Coordinator. Performs clinical and administrative coordination of sponsored clinical trial...
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...
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,...
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...
Clinical Research Coordinator – Neuroscience/Psychiatry Evanston, IL. Position: Research Coordinator. Experience: At least two years of experience in coordinating clinical trials (experience with neurosciences/psychiatry/behavioral clinical trials highly preferred). Coordinate and assist with multip...
Clinical Research Coordinator within the Ophthalmic Clinical Trials and TranslationalCenter (OCTTC) is responsible for managing, coordinating, and implementing allcomponents of clinical research protocols, including pre and post-researchactivities both within and outside the clinical setting. Clinic...
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. Recruit and interview potential study patients with guidance from PI and other clinica...
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 ...
Analyzes, facilitates, and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management, including patient data retrieval, referring MD office records, preparing clinical research charts, subject consenting, subject recruitm...
The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biol...
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...
The Clinical Research Coordinator 1 (CRC1) (Project -Based, 18 month) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of a departmental or lab research manager. Identifies and explains the responsibilities of Principal Investigators, resea...
The CRN will participate in required training and education programs, provide clinical research education to local clinic staff, and ensure site research quality by practicing in compliance with policies, SWIs, principles of Good Clinical Practice (GCP) and applicable federal, state, and local regul...
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;...
Certification as a clinical research coordinator (ACRP or SOCRA). Prior working experience involving clinical research protocol development. This position provides an opportunity to interact with the inpatient critical care team, screen complex medical patients, and implement state-of-the-art clinic...
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,...
Coordinate administrative and clinical aspects of multiple research projects. Certification specializing in Research Professional credentialed from the Public Responsibility in Medicine and Research (PRIM&R) preferred. Two years clinical research experience preferred. Collaborate with primary invest...
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...
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...
Knowledge of research protocols, principles,and procedures; knowledge of aspects of clinical trials such as screening,interviewing, knowledge of computer data management; knowledge of ethics andregulatory procedures (, informed consent process, data safety andmonitoring plans, principles of data col...
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...
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...
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 ...
The CRN will participate in required training and education programs, provide clinical research education to local clinic staff, and ensure site research quality by practicing in compliance with policies, SWIs, principles of Good Clinical Practice (GCP) and applicable federal, state, and local regul...