Clinical Trials Associate
VirtualVocationsSanta Clara, California, United Statesjob_description.job_card.variable_days_ago
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A company is looking for a Clinical Trials Associate responsible for clinical trials administration to ensure the effective conduct of clinical research studies.
Key Responsibilities
Support Clinical Operations teams in completing tasks to meet trial and project goals
Maintain and organize clinical study documentation, including preparation for audits and archival
Collaborate with Clinical Trials Manager and Clinical Research Associates to resolve documentation issues
Required Qualifications
Bachelor's degree with 0-2 years of clinical research experience, or a high school diploma with 5+ years of clinical research experience
Proficiency in MS Word, Excel, PowerPoint, Outlook, and Adobe
Knowledge of Good Documentation Practices (GDocP) and good documentation practices (GDP)
Ability to maintain corporate confidentiality at all times
Experience in clinical trial documentation and site management is preferred
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Clinical Trial Associate • Santa Clara, California, United States
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