U

University of Miami

Research university in Coral Gables, FL

Clinical Research Data Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeMiami, FL, USANo salary listedHybrid

About the Job

Requirements

  • High school diploma or equivalent/relevant experience.
  • No previous experience is required.
  • Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
  • Ability to work collaboratively with others and contribute to a team environment.
  • Proficiency in office software, technology, and relevant computer applications.
  • Strong written and verbal communication skills for interacting with colleagues and stakeholders.

Responsibilities

  • Assist in creating, updating, and maintaining research charts and case report forms, including regulatory-related issues, in accordance with department standard operating procedures, under the supervision of the Principal Investigator and supervisor.
  • Compile, register, and submit data; monitor compliance with the protocol; and ensure adherence to standard operating procedures and applicable regulations and guidelines.
  • Extract clinical and research data from electronic medical records and other sources, and enter it into clinical paper-based or electronic data capture systems for each assigned study.
  • Manage a workload of studies commensurate with experience level.
  • Answer data clarifications, including data queries, for each study.
  • Schedule and meet with study monitors, ensure patient cases are ready for monitor visits, and address items after each monitoring visit.
  • Develop source data worksheets specific to each assigned study.
  • Ensure clinical issues from monitoring reports are addressed and closed out before the next monitoring visit.
  • Ensure all study requirements are documented and meet internal and external regulations in accordance with protocol guidelines.
  • Maintain logs, including TAS submissions and Velos, in a timely manner according to department standard operating procedures.
  • Participate in site initiation visits, monitoring visits, site disease group team meetings, and Principal Investigator oversight meetings as required.
  • Assist the multidisciplinary team in research activities.
  • Maintain study binders and filings according to protocol requirements and department policy.
  • Adhere to University of Miami and department policies and procedures.
  • Compile patient data for Investigator review to determine patient eligibility for protocol enrollment.
  • Maintain screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation, and other sponsor- or protocol-specific logs.
  • Ensure the work environment is organized and functions efficiently.
  • Support the delivery of appropriate care and positive working relationships throughout the medical center through professional practice.
  • Safeguard University assets and adhere to University and unit-level policies and procedures.

About the Company

University of Miami

Research university in Coral Gables, FL

The University of Miami is a private research university focused on education, discovery, and service, with undergraduate, graduate, and professional programs.

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