Clinical Research Coordinator II
About The Position
The Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism is a national leader in research leading to the development of new insights in the treatment of endocrine diseases and disorders. Work in the areas of diabetes, thyroid and sleep disorders has been greatly advanced by The University of Chicago endocrinology faculty. Our research activities are supported by a number of different sources including the National Institute of Health (NIH) and non-federal granting agencies. The Section is home to one of 16 NIH funded Diabetes Research and Training Centers. Over the years, several members of the Endocrine faculty have led investigations that resulted in significant discoveries in the areas of diabetes, thyroid and sleep disorders. The Clinical Research Coordinator II (CRCII) is a specialized researcher, partnering with the clinical Principal Investigator (PI), Dr. Silvana Pannain in the Section of Endocrinology in the Department of Medicine. 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. Accountable for all tasks in moderately complex clinical studies. Performs other related work as needed.
Requirements
- Minimum requirements include a college or university degree in related field.
- Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
- Resume/CV (required)
- Cover Letter (required)
Nice To Haves
- Bachelors degree.
- Clinical research experience or relevant experience.
- Coordinating multiple studies, such as investigator initiated, industry sponsored, and multi-site trials.
- Aware of safety hazards and take appropriate precautions.
- Comprehend technical documents.
- Create and deliver presentations.
- Communicate in writing.
- Communicate orally.
- 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.
Responsibilities
- Recruit, screen, and enroll eligible study participants.
- Obtain informed consent and provide detailed study information to patients.
- Monitor patient status, collect clinical data, and report adverse events.
- Collect biospecimens according to protocol.
- Maintain accurate and timely documentation in compliance with Good Clinical Practice (GCP).
- Coordinate study visits, assessments, and follow-ups.
- Educate patients and families about clinical trials and research procedures.
- Ensure adherence to ethical guidelines, regulatory requirements, and institutional policies.
- Collaborate with investigators, study coordinators, and other healthcare staff.
- Prepare study-related reports and assist in regulatory submissions when needed.
- Present study findings and participate in research meetings and training as needed.
Benefits
- The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
