Clinical Research Data Specialist I - Clinical Trials Unit

  • University Hospitals
  • Cleveland, OH, USA
  • Feb 23, 2021

Job Description


  • Coordinate and facilitate the clinical trial data for participants enrolled in clinical research studies conducted by principal investigators at University Hospitals Cleveland Medical Center.
  • Assist and complete case report forms entry, review and abstraction required to conduct clinical research with the IRB, pharmaceutical sponsor, and other internal, external agencies or committees.
  • Provide timely and professional ongoing data entry of clinical trial data by identifying errors and inconsistencies of data in accordance with study submission completion guidelines across a variety of studies in different therapeutic areas and phases.
  • Assure that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with SOPs, GCP guidelines, sponsor guidelines and current regulations.

  • Bachelors Preferred
  • Associates Req with 4 yrs of exper in data related, research field
  • Cert in Human Subjects Protection must be obtained within 1 month of hire
  • Detail oriented person with the ability to work independently on multiple tasks and manage time effectively.
  • Medical terminology preferred.
  • Excellent verbal, written, interpersonal and written communication skills.
  • Basic knowledge of computer operations and demonstrated computer skills in a variety of software environments required Excel, Word, database applications.