We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Clinical Trial Associate II - Onsite in Aliso Viejo, CA

Glaukos Corporation
United States, California, Aliso Viejo
Aug 02, 2025

How you will make an impact:

The Clinical Trials Associate II is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director.

What you will you:

Clinical Study Preparation and Maintenance



  • Assists with review of clinical trial protocols
  • Assists with development/review of source documents
  • Assists with preparation of Informed Consent Forms
  • Assists with development of recruitment materials and study tools
  • Works with cross functional team members as assigned
  • Works with study vendors as assigned


Collection and Review of Site Start-Up Documents



  • Communicates directly with site staff to obtain site start-up documents
  • Negotiates study contract and budget
  • Prepares Regulatory Binders and provides to sites prior to Site Initiation Visit (SIV)Receives, QC's, and files site documents in Study Master File
  • Provides status of site documents in Study Master File to Clinical Research Associates (CRAs) prior to Monitoring Visits


Clinical Site Management



  • CTA is responsible for effective communication with clinical trial sites
  • Obtains site documents from Clinical Research Associates during trial
  • Addresses inquiries from sites and CRAs
  • Escalates issues to study management as needed


Study Master File Maintenance



  • Sets up Study Master File and Study Master File Tracker at the beginning of each study
  • Receives, QC's, scans and files documents in Study Master File
  • Provides status of documents to Clinical Management


Establishes and Maintains Tracking of Trial Information



  • Team and site contact information
  • Site status information
  • Equipment and supplies Enrollment trackers
  • Adverse event trackers
  • Site payment trackers and site payments


How You'll Get There:



  • Bachelor's Degree with background in science, or equivalent work experience preferred
  • 2-5 years clinical work experience in the bio- pharmaceutical or device industry, preferably within the ophthalmology field

Applied = 0

(web-6886664d94-b4mmp)