Clinical Research Data Specialist I - Clinical Trials Unit

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

Job Description

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.
Qualifications

  • 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.
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Schedule

Days

Salary

Competitive