Full-Time

Clinical Research Data Specialist

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (1)
Required Skills
Electronic Health Records (EHR)
Data Analysis

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Requirements
  • A high school diploma or equivalent is required.
  • The position requires accurate completion of assignments with attention to detail.
  • The position requires the ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
  • The position requires the ability to process and handle confidential information with discretion.
  • The position requires the ability to work evenings, nights, and weekends as necessary.
  • The position requires the ability to work independently and/or in a collaborative environment.
Responsibilities
  • Extract clinical and research data from electronic medical records and other sources and enter it into the clinical paper-based or electronic data capture system for each assigned study.
  • Manage a workload of studies commensurate with the level of experience.
  • Answer data clarifications and data queries for each study.
  • Schedule and meet with study monitors, ensure patient cases are ready for each monitor visit, and address items after each monitoring visit.
  • Develop source data worksheets specific to each assigned study.
  • Address and close out clinical issues from monitoring reports before the next monitoring visit.
  • Document all study requirements and ensure they meet internal and external regulations in accordance with protocol guidelines.
  • Maintain logs, including TAS submissions and Velos logs, 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 with research activities.
  • Maintain study binders and filings according to protocol requirements and department policy.
  • Adhere to University 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.
  • Maintain an organized and efficient work environment and contribute to a collaborative work environment.
  • Safeguard University assets and follow University and unit-level policies and procedures.

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