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Clinical Study Associate
VirtualVocationsPasadena, Texas, United Statesjob_description.job_card.variable_days_ago
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- serp_jobs.job_card.full_time
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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
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Clinical Associate • Pasadena, Texas, United States
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