Actalent - Houston, TX

posted 6 days ago

Part-time - Mid Level
Houston, TX
10,001+ employees
Administrative and Support Services

About the position

The Clinical Research Coordinator (CRC) position at Actalent involves supporting an ongoing Ophthalmology clinical trial. The role requires the candidate to work independently and manage various responsibilities related to clinical research, including data entry, regulatory support, and participant coordination. The position is contract-based and requires flexibility to assist with various tasks as needed throughout the study.

Responsibilities

  • Data entry & query resolution
  • Assist with Institutional Review Board (IRB) approvals and provide regulatory support
  • Create and maintain source documents
  • Organize participant schedules and ensure informed consent
  • Prepare necessary documentation and coordinate with the research team to ensure all protocols are followed
  • Assist with any other study-related efforts as deemed necessary by the site

Requirements

  • Minimum of two years of experience as a Clinical Research Coordinator
  • IATA certification required
  • Specific experience in Ophthalmology clinical trials preferred
  • Proficiency with electronic medical records (EMR) and electronic data capture (EDC) systems

Benefits

  • Pay range of $25.00 - $33.00 per hour
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