Hybrid Clinical Trials Data Specialist I

University Hospitals; Cleveland (OH); Hybrid; USD 52,000 - 72,000; Full time

Job summary

University Hospitals Case Medical Center is seeking a Clinical Research Data Specialist I to support data coordination for participants in clinical trials. This hybrid role involves entry, review, and abstraction of case report forms in collaboration with IRB, sponsors, and study teams.

The position emphasizes maintaining trial integrity, adhering to SOPs and GCP guidelines, and ensuring accurate data across diverse therapeutic areas.

Qualifications

• Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively.

Responsibilities

• Coordinate and facilitate the clinical trial data for participants enrolled in clinical research studies conducted by principal investigators at University Hospitals Case 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.

Skills

Detail-oriented

Data requirements communication

Medical terminology

Verbal and written communication

PC/software proficiency

Education

High School Equivalent / GED (Required)

Tools

Excel

Access

Word

Database applications

Job description

University Hospitals Case Medical Center is seeking a Clinical Research Data Specialist I to support data coordination for participants in clinical trials. This hybrid role involves entry, review, and abstraction of case report forms in collaboration with IRB, sponsors, and study teams.

The position emphasizes maintaining trial integrity, adhering to SOPs and GCP guidelines, and ensuring accurate data across diverse therapeutic areas.