Clinical Trials Data Specialist I (Hybrid)

Mobile; United States; Hybrid; USD 52,000 - 73,000; Full time

Job summary

University Hospitals Case Medical Center is seeking a Clinical Research Data Specialist I (Hybrid) to coordinate and manage data for participants enrolled in clinical studies. This role includes CRF entry, data review, and abstraction activities across multiple therapeutic areas and phases.

The position emphasizes timely data entry, data quality, and ensuring compliance with SOPs, GCP guidelines, and sponsor requirements, while maintaining confidentiality of PHI as part of standard procedures.

Qualifications

• High School GED required.
• Detail-oriented with ability to manage multiple tasks.
• Strong ability to understand and communicate data requirements.
• Excellent verbal and written communication skills.
• Basic knowledge of computer operations with experience in Excel, Access and Word.

Responsibilities

• Coordinate and facilitate clinical trial data for participants in University Hospitals Case Medical Center studies.
• Assist with case report forms entry, review and abstraction for studies.
• Provide timely data entry and identify errors per study guidelines across various trials.
• Ensure trial data integrity and compliance with SOPs, GCP guidelines and sponsor requirements.

Skills

Detail-oriented

Data requirements communication

Verbal and written communication

Time management

Education

High School Equivalent / GED

Tools

Excel

Access

Word

Database applications

Job description

University Hospitals Case Medical Center is seeking a Clinical Research Data Specialist I (Hybrid) to coordinate and manage data for participants enrolled in clinical studies. This role includes CRF entry, data review, and abstraction activities across multiple therapeutic areas and phases.

The position emphasizes timely data entry, data quality, and ensuring compliance with SOPs, GCP guidelines, and sponsor requirements, while maintaining confidentiality of PHI as part of standard procedures.