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Clinical Research Data Specialist I
University HospitalsClinical Research Data Specialist coordinating clinical trial data for participants at Seidman Cancer Center. Facilitating data entry, review, and ensuring quality in compliance with regulations.
About the role
Key responsibilities & impact- Coordinate and facilitate the clinical trial data for participants enrolled in clinical research studies conducted by principal investigator(s)
- Assist and complete case report forms entry, review and abstraction required to conduct clinical research
- Provide timely and professional ongoing data entry of clinical trial data by identifying errors and inconsistencies
- Assure that the integrity and quality of the clinical research trial is maintained
Requirements
What you’ll need- High School Equivalent / GED (Required)
- Detail-oriented person with the ability to work independently on multiple tasks
- Ability to understand and communicate data requirements to others
- Medical terminology (Preferred proficiency)
- Excellent verbal, written, interpersonal and written communication skills
- Basic knowledge of computer operations and demonstrated computer skills in a variety of software environments (ie Excel, Access, Word, database applications)
Benefits
Comp & perks- Annual training
- UH Code of Conduct
- UH policies and procedures for maintaining PHI
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data entrycase report forms entrydata reviewdata abstractionerror identificationdata integrityquality assurance
Soft Skills
detail-orientedindependent workcommunication skillsinterpersonal skillstime management
Certifications
High School EquivalentGED