Clinical Study Associate

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

Collaborate with study teams and Clinical Research Organisations to ensure compliance with established protocols

Track vendor budgets and invoices while monitoring patient enrollment and timelines

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 in Phase 2 and 3 studies and knowledge of global regulatory requirements is advantageous

Familiarity with Veeva Vault (CDMS and CTMS) and task management

Demonstrated ability to work independently and collaboratively within a team