Clinical Research Data Specialist II - Data Integrity

University of Miami; Miami (FL); Híbrido; USD 60.000 - 85.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits

Tuition remission

Medical coverage

Descripción de la vacante

The University of Miami/UHealth Department of SCCC is seeking a Full-Time Clinical Research Data Specialist 2 at the UHealth campus in Miami, FL. The role focuses on creating and maintaining research charts and case report forms with supervision from the PI and supervisor, ensuring timely data submission and protocol compliance.

Responsibilities include data extraction from EMRs, data validation, monitoring visits preparation, and collaboration with multidisciplinary teams to resolve data

Formación

• Learning agility: ability to learn new procedures, technologies, and protocols.
• Teamwork: ability to work collaboratively with others and contribute to a team environment.
• Technical proficiency: skilled in using office software, technology, and relevant computer applications.
• Communication: strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Responsabilidades

• Reviews and independently abstracts medical records for research participants across studies with moderate complexity.
• Extracts, validates, and enters clinical data from EMRs and source documents into data capture systems.
• Ensures data accuracy, completeness, and timeliness per protocol and study timelines.
• Responds to data clarifications and escalates complex issues as needed.
• Coordinates and supports routine monitoring visits with documentation and follow-up.

Conocimientos

Learning Agility

Teamwork

Technical Proficiency

Communication

Educación

High School Diploma or equivalent/relevant experience, certification or license

Descripción del empleo

The University of Miami/UHealth Department of SCCC is seeking a Full-Time Clinical Research Data Specialist 2 at the UHealth campus in Miami, FL. The role focuses on creating and maintaining research charts and case report forms with supervision from the PI and supervisor, ensuring timely data submission and protocol compliance.

Responsibilities include data extraction from EMRs, data validation, monitoring visits preparation, and collaboration with multidisciplinary teams to resolve data