Clinical Research Coordinator 1

• →Coordinate the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
• →Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
• →Recruit and interview potential study patients with guidance from PI and manager.
• →Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques.
• →Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.
• →Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.
• →Performs assessments at visits and monitors for adverse events.
• →Organizes and attends site visits from sponsors and other relevant study meetings.
• →Protect patients and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols.
• →Ensures Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.
• →Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.
• →Prepares for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
• →Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• →Accountable for all tasks in basic clinical studies.
• →Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
• →Performs other related work as needed.

• Bachelor's degree.

• Knowledge of medical terminology/environment.

• Ability to communicate with tact and diplomacy.
• Strong organizational skills.
• Strong communication skills (verbal and written).
• Excellent interpersonal skills.
• Strong data management skills and attention to detail.
• Knowledge of Microsoft Word, Excel and Adobe Acrobat.
• Ability to read and understand complex documents (e.g., clinical trial protocols).
• Ability to handle competing demands with diplomacy and enthusiasm.

• Resume (required)
• Cover Letter (required)

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FLSA Status

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Pay Range

The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.

The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.

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