Clinical Research Source Document Specialist

Job Summary

A company is looking for a Clinical Research Source Document Specialist.

Key Responsibilities

• Create and maintain source documents while ensuring compliance with regulations and protocols
• .Participate in study-related meetings and manage source document reviews from End Users
• .Track findings from source reviews and escalate discrepancies to the Process Quality Director

Required Qualifications

• Bachelor's degree
• Minimum of 2 years' experience in the clinical research industry, specifically with source documents
• Proficiency in Microsoft Office applications (Outlook, Word, Excel) and internet-based applications
• Strong work ethic and ability to work independently and collaboratively
• Adherence to HIPAA regulations and confidentiality standards