Clinical Study Associate

Job Summary

A company is looking for a Clinical Study Associate to support clinical study activities within Global Clinical Development Operations.

Key Responsibilities

• Support day-to-day clinical study activities, including regulatory inspection readiness and collaboration with study teams
• Maintain study team rosters, manage meeting agendas, and ensure TMF quality control for inspection readiness
• Track vendor budgets/invoices and assist with patient enrollment and metrics reporting

Required Qualifications

• Bachelor's degree in Life Sciences, Health Sciences, or a related field
• 1-2 years of experience in the pharmaceutical industry or clinical research organization
• Experience with Phase 2 and 3 studies and knowledge of global regulatory requirements is advantageous
• Familiarity with Veeva Vault (CDMS and CTMS) and task management
• Proven ability to work independently and collaboratively in a team environment