Clinical Research Coordinator 1 at The University of Chicago in Chicago, Illinois

Job Description:

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 job provides technical support activities related to documents, analyzes, and reports on clinical research data within the Department of Neurology at the University of Chicago. Provides input to support the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University.



Responsibilities

• Perform specific protocol procedures such as scheduling study visits and procedures, interviewing subjects, collecting and processing study specimens, taking vital signs, collecting study ECG's, etc.
  
  


• Understands study protocols and ensures all team members adhere to protocol specific procedures for patient safety and data quality assurance. Coordinates, completes and monitors the daily clinical trial activities and performs a variety of duties involved in the collection, compilation, documentation and reporting of clinical research data.
  
  


• Works under the general direction of a departmental, clinical research manager and/or the Office of Clinical Research (OCR) in partnership with the Principal Investigator (PI), Co-Investigator(s) and other study personnel.
  
  


• Works with the PI, clinical research manager, department, sponsoring agencies, and the OCR to support and provide guidance on the administration of the compliance, financial, and other related aspects of the clinical study.
  
  


• Plays a critical role in ensuring compliance with the study protocol, Federal guidelines, Local guidelines, and in accordance with Good Clinical Practice (GCP).
  
  


• Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
  
  


• Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  
  


• Performs other related work as needed.
  
  

Minimum Qualifications




Education:

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

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Work Experience:

Minimum requirements include knowledge and skills developed through ---
Certifications:




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Preferred Qualifications




Education:

• Bachelor's degree.
  
  

Experience:

• Research experience or related experience.
  
  


• Experience coordinating Neuroscience based clinical trials or previous experience coordinating complex clinical trials.
  
  


• Knowledge of medical terminology/environment.
  
  


• Phlebotomy experience.
  
  

Preferred Competencies

• Interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
  
  


• Work in teams.
  
  


• 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.
  
  


• Read and understand complex documents (e.g., clinical trial protocol).
  
  


• Handle competing demands with diplomacy and enthusiasm.
  
  


• Multi-task on multiple projects assign and prioritize.
  
  


• Adaptability to changing working situations and work assignments.
  
  


• Ability to absorb large amounts of information quickly.
  
  

Application Documents

• Resume/CV (required)
  
  


• Cover Letter (preferred)
  
  

When applying, the document(s) MUSTbe uploaded via the My Experience page, in the section titled Application Documents of the application.



Job Family



Research



Role Impact



Individual Contributor



FLSA Status



Exempt



Pay Frequency



Monthly



Scheduled
Weekly Hours



40



Benefits Eligible



Yes



Drug Test Required



Yes



Health Screen Required



Yes



Motor Vehicle Record Inquiry Required



No



Posting Statement



The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, national or ethnic origin, 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.


Staff 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.


We seek a diverse pool of applicants who wish to join an academic community that places the highest value on rigorous inquiry and encourages a diversity of perspectives, experiences, groups of individuals, and ideas to inform and stimulate intellectual challenge, engagement, and exchange.


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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