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Clinical Trials Coordinator

Company: PRiSMS GROUP LLC.
Location: Cicero
Posted on: May 14, 2018

Job Description:

We are looking for an aspiring seasoned professional for one of our Chicago-land locations. Responsibilities include: Provides research services, administrative support, and assistance to the Clinical Research Study Site Coordinator, Principal Investigator(s), and Sub-Investigators to facilitate clinical research protocols in Oncology, Cardiovascular, Endocrinology therapeutics. Assists the Clinical Research Study Site Coordinator with identifying the appropriate forms and processes necessary to complete the research protocol and coordinate statistical and scientific consultation from research staff. Advises on topics such as Good Clinical Practice, informed consent, study file management, and other related issues. Assists with coordinating research in accordance with approved protocol and applicable local and state and federal regulations, while promoting the safety and confidentiality of research subjects and their data at all times. Maintains complete and accurate study drug and equipment accountability at all times. Advises and provides oversight support to all study Research Assistants. Performs data collection by conducting research interviews. Recruits and screens subjects for research studies. Collects baseline and follow up data from subjects. Checks for validity and accuracy of data ensuring compliance with Quality Assurance requirements and clinical relevance. Performs other duties as assigned. Salary dependent on experience. Must have prior experience in Clinical Trials of minimum 1 year.

Keywords: PRiSMS GROUP LLC., Cicero, Clinical Trials Coordinator, Healthcare, Cicero, Illinois

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