Trabajos clinical research coordinator en Chicago, Illinois (IL) State

DEPARTMENT: 18383 - Safety & High ReliabilityLOCATION: 350 7th Street North, Naples, FL, 34102WORK TYPE: WORK SCHEDULE: ABOUT NCHNCH is an independent, locally governed non-profit delivering premier comprehensive care. Our healthcare system is comprised of two hospitals, an alliance of 700+ physi...

IRB applications, data safety and monitoring plans) involved with clinical trials and other clinical research; ability to work as a member of a project team; knowledge of clinical tasks required for research (e. This position manages and coordinates the timely handling of all components of clinic...

The Clinical Research Coordinator will coordinate the research component of the specified clinical program at the Shirley Ryan AbilityLab (SRAlab). The Clinical Research Coordinator will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values b...

This position is responsible for overseeing, organizing and implementing multiple clinical research trials being conducted. Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholder...

The Communication Bridge Research Program at the Healthy Aging & Alzheimer's Research Care (HAARC) Center, is seeking a Clinical Research Coordinator 2 to join our groundbreaking intervention study. The Healthy Aging & Alzheimer's Research Care (HAARC) Center, is a new multidisciplinary center at...

This position is responsible for overseeing, organizing and implementing multiple clinical research trials being conducted. Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholder...

The Travel Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This role will perform a variety of clinical and administrati...

Based out of the Chicago, IL area, the Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compli...

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 intere...

Completion of a research certification through accredited research professional organization such as ACRP. Previous clinical research experience involving direct interaction with participants including consenting. Background in healthcare and/or clinical research with experience collecting medica...

Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150286 Job Category University Staff Job Type Full-Time FLSA Status Non-Exempt Campus Maywood-Health Sciences Campus Department Name CBCC Research Location Code CBCC RESEARCH (06310A) Is this split and/or fully grant funded? Yes Duties a...

This position manages and coordinates the timely handling of all components of clinical research protocols, including pre and post research activities, internal and external to the clinical setting. Notify and inform physicians, clinical staff, affiliates and grant sponsors of adverse events and ...

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 inv...

News & World Report, found UIC climbed up in its rankings among top public schools in the nation and among all national universities. UIC has nearly 260,000 alumni, and is one of the largest ...

... Study Coordinator Qualifications: * Previous experience as a clinical technician or in other ... research site, that focuses upon early phase clinical research and particularly overnight ...

Location: Chicago, IL Job Description: Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.Recruits and interviews potential study patients with guidance from PI and other clinical res...

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...

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 inv...

Participates in subject screening and schedules research study participants for study visits. ...

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 recru...

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...

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, re...

Assists in monitoring and auditing of data for clinical research trials. Experience collaborating with multiple sites in clinical research. Familiarity with reviewing Serious Adverse Events (SAEs), CDAs and other clinical research specific documents. Leads execution & control of research data ba....

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 ...