Clinical Research Coordinator 2

University of Chicago

University of Chicago

Chicago, IL, USA
USD 60k-75k / year
Posted on Apr 23, 2025

Department

BSD NEU - Clinical Research Staff


About the Department

The Department of Neurology at The University of Chicago Medical Center has a great history and tradition, having made significant contributions to neurological training, clinical care, and the basic understanding of neurological disease.


Job Summary

The Clinical Research Coordinator 2 (CRC 2) is an onsite, patient-facing, specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the Clinical Research Manager. The CRC 2 supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities

  • Coordinates the conduct of clinical research studies from startup to closeout including IRB submissions, screening and recruitment of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence and data integrity.

  • Arranges and conducts clinical research visits.

  • Coordinates reimbursement of subjects.

  • Collects, processes, and ships biospecimen samples.

  • Data collection and entry.

  • Organizes and/or attends relevant study meetings.

  • Protects 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.

  • Ensures compliance with federal regulations and institutional policies.

  • May assist in the training of new or backup coordinators.

  • Accountable for all tasks in moderately complex clinical studies.

  • Assists with various professional, organizational, and operational tasks under moderate supervision.

  • Performs other related work as needed.


Minimum Qualifications

Education:

Minimum requirements include a college or university degree in related field.


Work Experience:

Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.


Certifications:

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Preferred Qualifications

Education:

  • Bachelor's degree.


Experience:

  • Clinical research experience or relevant experience.

  • Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).

Preferred Competencies

  • Strong communication skills (verbal and written).

  • Excellent interpersonal skills.

  • Adaptability to changing working situations and work assignments.

  • Ability to comprehend technical documents.

  • Ability to develop and manage interpersonal relationships.

  • Ability to exercise absolute discretion regarding confidential matters.

  • Ability to follow written and/or verbal instructions.

  • Ability to handle sensitive matters with tact and discretion.

  • Ability to pay attention to detail.

  • Ability to perform multiple tasks simultaneously.

  • Excellent time management and ability to prioritize work assignments.

  • Ability to train or teach others.

  • Working knowledge of Good Clinical Practices (GCP).

Application Documents

  • Resume (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

Research


Role Impact

Individual Contributor


Scheduled Weekly Hours

40


Drug Test Required

Yes


Health Screen Required

Yes


Motor Vehicle Record Inquiry Required

No


Pay Rate Type

Salary


FLSA Status

Exempt


Pay Range

$60,000.00 - $75,000.00

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

Yes

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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