Hiring.Camp

Clinical Research Coordinator II - Endocrinology

Uchicago

·

1 week ago

Salary
$60k – $75k
Location
Hyde Park Campus, United States of America
Workplace
Onsite
Type
Full-time
Department
Healthcare
Education
Bachelor
Closing date
Today
Source
Workday

Description

Department

BSD MED - Endocrinology - Pannain Research Staff


About the Department

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.


Job Summary

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.

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.

  • 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.


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:

---

Preferred Qualifications

Education:

  • Bachelors degree.

Experience:

  • Clinical research experience or relevant experience.

  • Coordinating multiple studies, such as investigator initiated, industry sponsored, and multi-site trials.

Technical Skills or Knowledge:

  • Aware of safety hazards and take appropriate precautions.

  • Comprehend technical documents.

  • Create and deliver presentations.

Preferred Competencies

  • 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.​

Application Documents

  • Resume/CV (required)

  • Cover Letter (required)


The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions.

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.

 

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.

Skills

ReactGCPClinical TrialsCompliance

Similar Jobs

30

Clinical Research Coordinator

Mayo Clinic · Rochester, MN, United States, US

Yesterday

Clinical Research Coordinator

Guidehouse is · Client Office: Bethesda, MD, United States of America · Onsite

Yesterday

Clinical Research Coordinator

Ochsner · Ochsner Medical Center - New Orleans, United States of America

Yesterday

Clinical Research Coordinator

Franciscanalliance · IN - Indianapolis, United States of America

Yesterday

Clinical Research Coordinator

Axle · Bethesda, MD

Yesterday

Clinical Research Coordinator

Massgeneralbrigham · 165 Cambridge Street Boston (Charles River Plaza East), United States of America · Onsite

2 days ago

Clinical Research Coordinator

Cardiovascular Associates of America · Orlando, FL · Onsite

3 days ago

Clinical Research Coordinator

Alcanza Clinical Research · Coastal Carolina Research Center | Charleston, SC

5 days ago

Clinical Research Coordinator

Avispa Technology · Palo Alto, CA, US · Hybrid, Onsite

5 days ago

Clinical Research Coordinator

Northwestern Medicine · Winfield, IL, United States

5 days ago

Clinical Research Coordinator

Massgeneralbrigham · 149 Thirteenth Street Building 149 Charlestown (Building 149), United States of America +1 · Onsite

6 days ago

CLINICAL RESEARCH COORDINATOR

Northwest Specialty Hospital · Post Falls, ID

6 days ago

CLINICAL RESEARCH COORDINATOR

Key Whitman Eye Center · Post Falls, ID

6 days ago

Clinical Research Coordinator

Eurofins Scientific · Piscataway, NJ, United States

6 days ago

Clinical Research Coordinator

Career Opportunities · Silver Spring, MD, United States of America

1 week ago

Clinical Research Coordinator

United Derm Partners · Spokane Valley, WA

1 week ago

Clinical Research Coordinator

Avera Careers · Avera Cancer Institute-Sioux Falls, United States of America

1 week ago

Clinical Research Coordinator

Icon · US, Blue Bell (ICON), United States of America · Onsite

1 week ago

Clinical Research Coordinator

Imh · Intermountain Health Intermountain Medical Center, United States of America · Onsite

1 week ago

Clinical Research Coordinator

Alcanza Clinical Research · Desert Clinical - Henderson, NV

1 week ago

Clinical Research Coordinator

OhioHealth is · RIVERSIDE METHODIST HOSPITAL, United States of America

1 week ago

Clinical Research Coordinator

Imh · Intermountain Health LDS Hospital, United States of America +1 · Onsite

1 week ago

Clinical Research Coordinator

Nymc Touro · Hawthorne, NY, US

1 week ago

Clinical Research Coordinator

Aoncology · Genesis Cancer and Blood Institute, United States of America

1 week ago

Clinical Research Coordinator

Alcanza Clinical Research · Tampa Bay Medical Research - Largo

1 week ago

Clinical Research Coordinator

Foundation for Atlanta Veterans Education and Research · Decatur, GA

1 week ago

Clinical Research Coordinator

Urology of Virginia PLLC · Virginia Beach, VA

1 week ago

Clinical Research Coordinator

MNGI · Minneapolis, MN

1 week ago

Clinical Research Coordinator

74000165 FlexStaff N - ClinaCore · Staten Island, Richmond, United States, US

1 week ago

Clinical Research Coordinator

Mayo Clinic · Phoenix, AZ, United States, US

1 week ago