Clinical Study Associate

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

Key Responsibilities

Provide support for day-to-day clinical study activities, including regulatory inspection readiness

Collaborate with study teams and Clinical Research Organisations to ensure effective execution of clinical studies

Track vendor budgets and invoices, and maintain organized lists of Standard Operating Procedures (SOPs)

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 global / international studies is advantageous

Knowledge of global / regional regulatory and compliance requirements for clinical research

Familiarity with Veeva Vault (CDMS and CTMS) is preferred