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Job details

Clinical Research Coordinator 1

Department

BSD MED - Pulmonary - Clinical Research Staff


About the Department

The University of Chicago’s Respiratory Clinical Research team assists Principal Investigators in conducting drug trials, device trials, observational studies, databases, and biorepositories for a range of pulmonary diseases. The clinical research core provides support to nine Principal Investigators, who conduct both industry sponsored and grant funded projects (federal and foundation).


Job Summary

The Clinical Research Coordinator 1 (CRC 1) provides support to the faculty of the Section of Pulmonary/Critical Care within the Department of Medicine. The CRC 1 works with the PI, Co-Investigator(s), department, sponsoring agencies, and/or the to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study.

Responsibilities

  • Coordinate all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.

  • Maintain accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.

  • Plan and coordinate patient schedule for study procedures, return visits, and study treatment schedules.

  • Ensure Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.

  • Prepare and maintains protocol submissions and revisions.

  • Educate patients about study procedures to be performed, visit schedule, what to report between and during visits, and potential side effects.

  • Perform assessments at visits and monitors for adverse events.

  • Organize and attend site visits from sponsors and other relevant study meetings.

  • May recruit and interview potential study patients. May obtain, possess, and transport specimens to appropriate laboratory according to established aseptic techniques.

  • 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.


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 years of work experience in a related job discipline.


Certifications:

---

Preferred Qualifications

Education:

  • Bachelor's degree.


Experience:

  • Experience with clinical coordinating.

  • Experience with REDCap.

  • Experience with primary data entry and analysis.

  • Experience working with human research subjects.
     

Preferred Competencies

  • Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.

  • 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 understand complex documents (e.g., clinical trials).

  • Ability to handle competing demands with diplomacy and enthusiasm.

  • Ability to absorb large amounts of information quickly.

  • Adaptability to changing working situations and work assignments.

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

$50,000.00 - $65,000.00

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.

 

The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: http://securityreport.uchicago.edu. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.

Average salary estimate

$57500 / YEARLY (est.)
min
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$50000K
$65000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Clinical Research Coordinator 1, UChicago Medicine

Are you looking for an exciting opportunity in clinical research? Join the University of Chicago's Respiratory Clinical Research team as a Clinical Research Coordinator 1 in Chicago, IL! In this role, you'll be integral in assisting our Principal Investigators (PIs) with drug trials, device trials, and observational studies focusing on various pulmonary diseases. Your day-to-day activities will involve coordinating clinical trials by managing patient enrollment, follow-ups, and ensuring compliance with regulations. You'll maintain meticulous documentation, including informed consent and Case Report Forms (CRFs), while efficiently educating patients about their study procedures and potential side effects. This position fosters a collaborative environment where you'll interact with PIs, Co-Investigators, and various agencies, helping to ensure the success of our research initiatives. If you are detail-oriented and passionate about advancing pulmonary medicine, we want to hear from you! With a supportive team and opportunities for professional growth, the University of Chicago is committed to fostering your career in clinical research. So if you have a background in a related field and less than two years of experience, apply today to be part of an impactful team that contributes to groundbreaking research!

Frequently Asked Questions (FAQs) for Clinical Research Coordinator 1 Role at UChicago Medicine
What responsibilities does the Clinical Research Coordinator 1 at the University of Chicago undertake?

The Clinical Research Coordinator 1 at the University of Chicago plays a vital role in coordinating clinical trials, which includes managing patient enrollment, follow-ups, and ensuring adherence to regulatory guidelines. The role also involves maintaining comprehensive documentation, preparing protocol submissions, and educating patients about study procedures.

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What qualifications are necessary for the Clinical Research Coordinator 1 position at the University of Chicago?

To qualify for the Clinical Research Coordinator 1 position at the University of Chicago, applicants need a college degree in a related field and must have knowledge and skills typically developed through less than two years of work experience in a relevant discipline. Preferred qualifications include a Bachelor’s degree and familiarity with clinical coordinating.

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How does one apply for the Clinical Research Coordinator 1 role at the University of Chicago?

Interested candidates can apply for the Clinical Research Coordinator 1 role at the University of Chicago by submitting a resume and cover letter through the My Experience page of the application portal. Make sure to upload the required documents in the designated section.

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What benefits can a Clinical Research Coordinator 1 expect at the University of Chicago?

As a Clinical Research Coordinator 1 at the University of Chicago, you can expect a comprehensive benefits package, which includes health insurance, retirement plans, and generous paid time off. Detailed information about benefits can be found in the University’s Benefits Guidebook.

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Is experience with REDCap beneficial for the Clinical Research Coordinator 1 role at the University of Chicago?

Yes, experience with REDCap is considered a preferred qualification for the Clinical Research Coordinator 1 role at the University of Chicago. Familiarity with REDCap can greatly assist in data management and primary data entry tasks essential to the role.

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Common Interview Questions for Clinical Research Coordinator 1
What experience do you have with coordinating clinical trials as a Clinical Research Coordinator 1?

When discussing your experience, be specific about the trials you have coordinated. Mention your roles in patient recruitment, data management, and adherence to regulatory guidelines, emphasizing any successful outcomes from those trials.

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How do you ensure compliance with regulatory guidelines in clinical research?

To ensure compliance, outline how you stay updated on regulatory requirements and the protocols you follow. Mention any specific training or certifications you may have and your attention to detail in maintaining documentation.

Join Rise to see the full answer
Describe a time when you had to handle a challenging situation with a study participant.

Share a specific incident that showcases your problem-solving skills. Detail the challenge, the steps you took to resolve it, and the outcome, highlighting your communication skills and empathy as a Clinical Research Coordinator.

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What strategies do you use to manage multiple clinical trials simultaneously?

Discuss your organizational skills and any tools or methods you use to prioritize tasks. For instance, you might mention maintaining a detailed calendar, utilizing project management software, and consistent communication with team members to keep everything on track.

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How would you educate patients about study procedures and potential side effects?

Explain your approach to patient education, focusing on clear and empathetic communication. You might include how you assess patients’ understanding and encourage questions to ensure they feel supported and informed about their participation.

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What is your experience with data management systems like REDCap?

Share your proficiency with REDCap and how you have utilized it in previous roles for data entry and management. Highlight your ability to analyze data and ensure accuracy, essential skills for a Clinical Research Coordinator.

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Can you describe your experience with obtaining informed consent from study participants?

Discuss your understanding of the informed consent process and your approach to ensuring participants are fully informed. Share examples of how you've communicated complex information in a clear and approachable manner.

Join Rise to see the full answer
What aspects of clinical research do you find most rewarding?

Share personal insights about what motivates you in clinical research—such as contributing to advancements in medicine, helping patients, or being part of a dedicated research team. Authenticity here will resonate with interviewers.

Join Rise to see the full answer
How do you handle competing demands and prioritize tasks as a Clinical Research Coordinator?

Provide an example of a time you successfully managed competing demands, outlining your decision-making process and tools you used to prioritize effectively. This shows your ability to stay organized and focused under pressure.

Join Rise to see the full answer
What role do you think communication plays in the Clinical Research Coordinator position?

Emphasize the importance of clear and effective communication in your role as a Clinical Research Coordinator. Discuss how it facilitates collaboration among stakeholders and ensures patients feel informed and comfortable throughout their study journey.

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Photo of the Rise User
Inclusive & Diverse
Rise from Within
Mission Driven
Diversity of Opinions
Work/Life Harmony
Transparent & Candid
Growth & Learning
Fast-Paced
Collaboration over Competition
Take Risks
Friends Outside of Work
Passion for Exploration
Customer-Centric
Reward & Recognition
Feedback Forward
Rapid Growth
Medical Insurance
Paid Time-Off
Maternity Leave
Mental Health Resources
Equity
Paternity Leave
Fully Distributed
Flex-Friendly
Some Meals Provided
Snacks
Social Gatherings
Pet Friendly
Company Retreats
Dental Insurance
Life insurance
Health Savings Account (HSA)

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Full-time, on-site
DATE POSTED
April 6, 2025

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