A company is looking for a Clinical Trial Assistant to manage documents and administrative tasks related to clinical trials.
Key Responsibilities
Manage trial documents and logistical tasks for clinical trial feasibility, start-up, execution, and close-out
Ensure compliance with GCP, local regulatory requirements, and relevant client SOPs
Track clinical trial progress, manage study data and budgets, and maintain trial protocol information in management systems
Required Qualifications
BA / BS degree in Life Sciences, Nursing, or a related scientific field (or equivalent experience)
1-2 years of relevant clinical trial experience preferred
Proficient in MS Office (Word, Excel, Access, Outlook, PowerPoint)
Experience in VeevaVault TMF is desirable
Legally authorized to work in the United States without requiring employment visa sponsorship
Clinical Trial • Greenville, South Carolina, United States