Clinical Research Coordinator I
Job details
- Location
- Chicago, Illinois
- Work type
- Onsite
- Compensation
- $50,000 - $65,000/yr
- Posted
- 4 days ago
- Apply on
- uchicago.wd5.myworkdayjobs.com
About this role
Department
BSD MED - Genetic Medicine - Gilad Research Staff
About the Department
Job Summary
We are seeking an experienced Clinical Research Coordinator I to support the implementation of a research project involving patient tissue samples. Key responsibilities include assisting with patient recruitment for basic research studies, walking patients through the process of informed consent, storing and transporting blood samples from the hospital to the laboratory, and preparing samples for DNA extraction. The incumbent will also participate in the management of day-to-day operations of a basic research laboratory, developing and optimizing protocols, and maintaining detailed and accurate records of pertinent lab data.
This is an on-site, patient-facing, specialized researcher partnering with the Principal Investigator (PI) and under the direction of a departmental or lab research manager.
Responsibilities
Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.
Supports regulatory compliance efforts in accordance with governmental and departmental protocols. Implements, organizes and maintains regulatory compliance records.
Coordinates with clinical staff to facilitate patient recruitment and informed consent.
Collects, stores, and transfers samples from University of Chicago Medicine locations to the Gilad Laboratory.
Develops procedures to ensure safety, security, quality, and accuracy of results.
Solves complex problems relating to the administration of projects, including planning new procedures, adapting existing procedures to the needs of the project, and making significant contributions to methodology.
Responds to email communications and other requests promptly and courteously.
Collects and enters data.
Maintains laboratory supplies inventory by checking stock to determine inventory level, anticipating needed supplies, placing and expediting orders for supplies, verifying receipt of supplies.
Maintains laboratory equipment performance by establishing quality standards; developing operations, quality, and troubleshooting procedures; ensuring staff compliance; certifying instrument performance; arranging equipment service and repair.
Accountable for all tasks in basic clinical studies.
Assists with various professional, organizational, and operational tasks under direct supervision.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
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Preferred Qualifications
Education:
Bachelors degree.
Experience:
Clinical research experience or relevant experience.
Experience working in a research laboratory.
Technical Skills or Knowledge:
Aware of safety hazards and take appropriate precautions.
Comprehend technical documents.
Create and deliver presentations.
Preferred Competencies
Oral and written communication.
Condense complicated issues to simple summaries that can be understood by a variety of constituents.
Develop and manage interpersonal relationships.
Exercise absolute discretion regarding confidential matters.
Follow written and/or verbal instructions.
Give directions.
Handle sensitive matters with tact and discretion.
Handle stressful situations.
Learn and develop skills.
Maintain a high level of alertness.
Pay attention to detail.
Perform multiple tasks simultaneously.
Prioritize work and meet deadlines.
React effectively, quickly, calmly, and rationally during conflicts and emergencies.
Train or teach others.
Work effectively and collegially with little supervision or as member of a team.
Work independently.
Application Documents
Resume/CV (required)
Cover Letter (required)
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Role Impact
Scheduled Weekly Hours
Drug Test Required
Health Screen Required
Motor Vehicle Record Inquiry Required
Pay Rate Type
FLSA Status
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.
Benefits Eligible
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.
Posting Statement
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.
Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.
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