Clinical Research Data Specialist I

Posted 4 Days Ago
Be an Early Applicant
Los Angeles, CA, USA
In-Office
27-31 Hourly
Entry level
Edtech
The Role
Support urologic oncology research by identifying and screening eligible patients, obtaining informed consent, collecting and entering clinical data, maintaining research databases, performing data quality checks, assisting follow-up and biospecimen documentation, and ensuring compliance with HIPAA, IRB, ICH/GCP and institutional policies.
Summary Generated by Built In

The University of Southern California (USC), founded in 1880, is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the "Trojan Family," which is comprised of the faculty, students and staff that make the university what it is.

USC’s Keck School of Medicine, Institute of Urology, is seeking a Clinical Research Data Specialist I to join our Clinical Research Database Unit. This position supports one of the nation's premier urologic oncology research programs by managing high-quality clinical research data that drive scientific discovery, translational research, and improvements in patient care.

Essential job duties include but are not limited:

  • Identify eligible patients for research studies.

  • Screen patients for study eligibility using medical records and research protocols.

  • Obtain informed consent from research participants.

  • Collect and enter clinical research data into study databases.

  • Review electronic medical records to ensure accurate and complete data collection.

  • Maintain research databases and update patient information as needed.

  • Perform routine data quality checks to ensure data accuracy and completeness.

  • Assist with patient follow-up and outcomes data collection.

  • Prepare research records and study documentation in accordance with institutional and regulatory requirements.

  • Assist with biospecimen collection and documentation, when applicable.

  • Work closely with physicians, research staff, and other team members to support ongoing research projects.

  • Maintain confidentiality and comply with HIPAA, IRB, and institutional research policies.

  • Perform other related duties as assigned.

Required Qualifications:

  • 1 year of clinical trial experience

  • Must have a strong attention to detail to ensure adherence to study SOPs and compliance with regulatory standards (ICH, GCP, HIPAA, etc)

Preferred Qualifications:

  • Experience using REDCap, Microsoft Access, SQL Server, or other clinical research database systems

  • Experience performing medical record abstraction and clinical data collection.

  • Knowledge of medical terminology, oncology, or urology.

  • Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.

  • A cooperative and team-oriented attitude

This position is on-site and employee must report to work at the USC Health Science Campus in Los Angeles, CA when scheduled. Work hours may be subject to change depending on business needs.

The hourly budgeted range for this position is $26.77 - $30.57. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations

Minimum Education: Associate's degree, Combined experience/education as substitute for minimum education
Minimum Experience: 6 months
Minimum Field of Expertise: Requires good attention to detail with prior data entry experience. Some knowledge of medical terminology.

                                                  

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying. 

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at [email protected]. Inquiries will be treated as confidential to the extent permitted by law.

  • Notice of Non-discrimination
  • Employment Equity
  • Read USC’s Clery Act Annual Security Report
  • USC is a smoke-free environment
  • Digital Accessibility

                                                  

If you are a current USC employee, please apply to this  USC job posting in Workday by copying and pasting this link into your browser:

https://wd5.myworkday.com/usc/d/inst/1$9925/9925$151546.htmld

Skills Required

  • 1 year of clinical trial experience
  • Strong attention to detail and adherence to study SOPs and regulatory standards (ICH, GCP, HIPAA)
  • Associate's degree or equivalent combination of experience/education
  • Prior data entry experience
  • Some knowledge of medical terminology
  • Experience using REDCap, Microsoft Access, SQL Server, or other clinical research database systems
  • Experience performing medical record abstraction and clinical data collection
  • Knowledge of oncology or urology
  • Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research
  • Cooperative and team-oriented attitude
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HQ: Los Angeles, CA

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