Clinical Research Data Assistant

Rovia Clinical ResearchBastrop, LA
$18 - $20

About The Position

The Clinical Research Data Assistant is responsible for accurately entering, reviewing, and maintaining study data within the EDC system and CTMS. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

Requirements

  • Strong knowledge of medical terminology and clinical procedures.
  • Understanding of ICH/GCP and regulatory requirements.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and patient-facing communication skills.
  • Ability to multitask and manage competing priorities in a fast-paced environment.
  • Proficiency in Microsoft Office, EDC, and CTMS applications.
  • Ability to work both independently and collaboratively.
  • High level of professionalism and commitment to patient confidentiality.

Nice To Haves

  • Bachelor’s degree in related field preferred.
  • Previous experience in data entry, healthcare administration, or research preferred.
  • Strong interest in a clinical research career.

Responsibilities

  • Enter clinical research data into EDC systems accurately.
  • Review source documents and transcribe data electronically.
  • Verify data completeness, consistency, and accuracy.
  • Assist with data cleaning activities and resolution of queries.
  • Organize and maintain study files, regulatory binders, and research documentation.
  • Maintain confidentiality of participant information and research records.
  • Perform other duties as assigned.
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