University of Chicago Clinical Research Coordinator 2 in Chicago, Illinois
Please make sure to read the job posting in its entirety as it reflects both the University roles and responsibilities, followed by the specific description.
2012211 Medicine-Infectious Diseases
About the Unit
The Chicago Center for HIV Elimination (CCHE), is situated within the Biological Sciences Division at the University of Chicago Medicine. CCHE aims to eliminate all new HIV transmission events by 2041. The University of Chicago's position on the South Side makes it uniquely situated to test, treat, and prevent new HIV infections in a highly affected population. The South Side communities and majority Black suburbs connected to them to the South represents the largest contiguous Black population in the United States. By using our integrated HIV transmission elimination approaches, we are beginning to make new infections in these communities less frequent.
Responsible for all aspects of research projects and research facilities. Plans and conducts clinical and non-clinical research; facilitates and monitors daily activities of clinical trials or research projects. Directs engineering and technical support activities to develop and maintain tools and computational methods needed to gather and analyze data.
Career Track and Job Level
Manages, facilitates, and monitors the daily activities of clinical research and clinical trials. Performs a variety of duties involved in the collection, documentation, analysis and reporting of clinical research and clinical trial data. Manages the strategic, administrative, operational, and financial decisions that impact clinical research and clinical trials conducted across the University.
P1: Performs routine assignments in the entry level to a professional job progression. Typically requires a college or university degree or the equivalent work experience that provides knowledge and exposure to fundamental theories, principles and concepts. Develops competence by performing structured work assignments. Uses existing procedures to solve routine or standard problems. Receives instruction, guidance and direction from others.
The job performs routine assignments related to the documentation, analysis, and reporting of research data. Provides input to support the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University.
1) Performs various aspects of clinical research, such as collecting and processing specimens, interviewing subjects, taking vital signs, and contributing to the case report., 2) Analyzes protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics., 3) Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups., 4) Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports., 5) Performs other related work as needed.
1) Oversee day to day operations of CDC and NIH funded projects that involve working with LGBTQ populations vulnerable to HIV.
2) Coordinate multiple related projects to ensure optimal recruitment, enrollment and fidelity to the complex requirements of study participation and follow-up visits.
3) This will include assistance with the development of study protocols, survey instruments, and maintenance of databases.
4) Conduct study interviews and recruit individuals from the community.
5) Work closely with the study PIs and Research Manager for the Center.
1) Demonstrated effective leadership and teaching skills.
2) Supervisory skills.
3) Strong knowledge of program subject matter.
4) Willingness to attend necessary orientation and trainings through Chicago.
5) Strong interpersonal skills and the ability to work both independently and as part of a team.
8) Ability to manage stressful situations.
9) Ability to maintain confidentiality.
10) Ability to work on multiple projects simultaneously, set priorities, and meet deadlines.
11) Proficiency in the use of Microsoft Applications, including but not limited to Outlook, Excel, Access and Word.
12) Demonstrated written and verbal communication skills and strong analytical skills.
13) Ability to sit for up to 2 hours.
14) Ability to use computers extensively for 4 hours or more.
15) Ability to stand for 4 hours or more.
16) Ability to bend, crouch, or stoop.
Education, Experience, and Certifications
Minimum requirements include a college or university degree in related field.
Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
1) Two years of clinical research experience or relevant experience
2)Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials)
2) Cover letter
Note:When applying, all required documents MUSTbe uploaded under the Resume/CV section of the application
Depends on Qualifications
Scheduled Weekly Hours
Drug Test Required
Health Screen Required
Motor Vehicle Record Inquiry Required
Remove from Posting On or Before
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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.
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- Posted 30+ Days Ago
- Full time