Clinical Research Coordinator 1 - Pediatrics
University of Chicago•Chicago, IL
•Onsite
About The Position
The Clinical Research Coordinator (CRC) 1 in Pediatrics provides research support within the Department of Pediatrics. The CRC 1 works under the general direction of the Director of Clinical Research, a principal investigator (PI), and the study team. The CRC 1 will be involved in multiple research trial types: multi-centered cooperative group and intergroup studies at a national level, multi-institutional pharmaceutical trials, and multi-centered trials designed, implemented and coordinated in a disease-specific Section.
Requirements
- Minimum requirements include a college or university degree in related field.
- Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
- Proficient in data management and knowledgeable in Microsoft Word, Excel, and Adobe Acrobat.
- Read and comprehend complex documents, such as clinical trials.
Nice To Haves
- Bachelor’s degree.
- 1-year clinical research experience or relevant experience.
- Excellent written and oral communication skills, including follow written and verbal instructions.
- Strong interpersonal skills to work independently and collaboratively as part of a team.
- Demonstrated discretion, tact, and professionalism in handling confidential and sensitive matters.
- Adaptable and committed to ongoing learning and skills development.
- Prioritize tasks, manage multiple deadlines, and maintain attention to detail.
Responsibilities
- Ensures standard operating procedures (SOP) are implemented and documented in accordance with study sponsor, PI, and regulatory agency specifications.
- Ensures compliance with federal regulations and institutional policies.
- Coordinates all aspects of conducting clinical trials including recruitment, screening, enrollment, education about study procedures, subject follow-up, completion of the case report form, and adverse event reports.
- Participates in study-related documentation, such as protocol worksheets, procedural manuals, institutional review board documents, or progress reports.
- Aliquot and prepares experimental and clinical samples for freezing.
- Ensures accurate storage for all specimen types, including blood and plasma samples.
- Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, case report forms (CRFs), and study-related communication.
- Understands the IRB submission and review process, and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions independently.
- Accountable for all tasks in basic clinical studies.
- Assists with various professional, organizational, and operational tasks under direct supervision.
- Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
- Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
- Performs other related work as needed.
Benefits
- health, retirement, and paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
