Clinical Research Data Manager I

Care2Prevent; Chicago (IL); On-site; USD 50,000 - 65,000; Full time

Job summary

The University of Chicago is seeking a Clinical Research Data Manager I to support clinical research data collection, entry, analysis, and reporting for low-complexity studies. This onsite role in Chicago, IL involves working with PIs and sponsors to ensure data integrity and regulatory compliance.

Responsibilities include assisting with documents, QA reviews, and preparing analysis materials under supervision. A strong eye for detail and teamwork are essential for success.

Qualifications

• Requires college/university degree in a related field.
• Minimum < 2 years of work experience in a related job discipline.

Responsibilities

• Performs data management tasks for low complexity clinical studies under supervision.
• Collects and reviews documents (medical records) with confidentiality.
• Prepares study-related documentation (protocol worksheets, reports, IRB docs).
• Supports quality assurance reviews and ensures data integrity.

Skills

Attention to detail

Organizational skills

Time management

Communication

Adaptability

Reading complex documents

Independent work

Education

Bachelor's degree in related field

Job description

Clinical Research Data Manager I - Logo### Clinical Research Data Manager IApply: Onsite: Chicago, IL: Full time: Posted Today: JR35742**Department**BSD MED - Hematology and Oncology - Clinical Research Data Managers - Cluster 5**About the Department**The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient care and clinical discovery. Ranked among the finest cancer programs in the country, the Section is comprised of nationally and internationally known faculty with expertise in all major types of malignancies, blood disorders, and experimental therapies.**Job Summary**The job performs routine tasks associated with the collection, entry, analysis, and reporting of clinical research data for low-complexity clinical research studies, ensuring accuracy and compliance with standard procedures. Participates in maintaining data integrity, quality review, and contributes to documentation efforts for clinical research conducted across the University. The Clinical Research Data Manager I will perform a variety of data management duties in support of clinical research studies conducted by principal investigators (PIs) for the clinical research program to ensure adherence to protocols and quality of information received.**Responsibilities*** Works on trials directly assigned. Works on industry sponsored trials which provide consistent monitoring/oversight.* Assist senior staff maintain high enrolling studies.* Accountable for all data management tasks in support of low complexity clinical research studies under direct supervision.* In collaboration with the principal investigator (PI), assists with collecting and reviewing documents such as medical records, while maintaining a high degree of confidentiality.* Participates in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated internal review groups.* Prepares study-related documentation for analysis, such as protocol worksheets, 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.**Work Experience:**Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.**Certifications:****---****Preferred Qualifications****Education:** * Bachelors degree.**Experience:** * Minimal medical/science related education or position.**Preferred Competencies** * Absorb large amounts of information quickly.* Adaptability to changing working situations and work assignments.* Attention to detail.* Interact and communicate (verbal and written) with clarity, tact, and courtesy with patrons, sponsors, staff, faculty, students, and others.* Organizational skills.* Read and understand complex documents.* Time management.* Ability to work independently and as part of a team.**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**No**Health Screen Required**No**Motor Vehicle Record Inquiry Required**No**Pay Rate Type**Salary **FLSA Status**Exempt **Pay Range**$50,000.00 - $65,000.00The 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**YesThe 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.