Clinical Research Data Specialist I, Clinical Trials

University Hospitals

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

Posted 10/3/2026full-timeCleveland • Ohio • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial data management, ensuring compliance with SOPs, GCP guidelines, and PHI security requirements while maintaining data integrity and quality across various studies. Proficient in data entry and communication of data requirements to stakeholders.

Highest-signal resume keywords

Clinical Trial Data ManagementSOP ComplianceGCP GuidelinesData Entry SkillsProtected Health Information (PHI) Security

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data EntryCase Report Form AbstractionData ReviewData Error IdentificationClinical Research Knowledge

Soft Skills

Detail-OrientedTime ManagementInterpersonal CommunicationWritten Communication

Tools & Technologies

ExcelAccessWordDatabase Applications

Certifications & Qualifications

High School Equivalent / GED

Industry Keywords

Clinical ResearchIRBPharmaceutical SponsorsStudy Submission GuidelinesCurrent Regulations

About the role

Key responsibilities & impact

Coordinate and facilitate clinical trial data for participants enrolled in clinical research studies conducted by principal investigators at University Hospitals Case Medical Center
Assist with and complete case report form entry, review, and abstraction for clinical research involving the IRB, pharmaceutical sponsors, and internal/external agencies or committees
Perform timely, professional data entry of clinical trial data across studies in different therapeutic areas and phases
Identify data errors and inconsistencies according to study submission and completion guidelines
Maintain the integrity and quality of clinical research trials
Ensure trials are conducted in accordance with SOPs, GCP guidelines, sponsor guidelines, and current regulations
Perform other duties as assigned
Comply with organizational policies and standards
Safely and securely maintain Protected Health Information (PHI)

Requirements

What you’ll need

High School Equivalent / GED (Required)
Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively
Ability to understand and communicate data requirements to others
Excellent verbal, written, interpersonal and written communication skills
Basic knowledge of computer operations and demonstrated computer skills in Excel, Access, Word, and database applications
Ability to comply with SOPs, GCP guidelines, sponsor guidelines, current regulations, and PHI security requirements
Ability to travel 10%

Benefits

Comp & perks

Annual training
UH Code of Conduct and UH policies and procedures addressing appropriate use of Protected Health Information (PHI)