A company is looking for a Source Creation Specialist to create and maintain source documents while ensuring compliance with relevant standards and regulations.
Key Responsibilities
Create and maintain source documents in compliance with established SOPs and applicable regulations
Participate in study-related meetings and manage source document reviews from End Users
Track findings from source reviews for future improvements and escalate any discrepancies to the Process Quality Director
Required Qualifications
Bachelor's degree or equivalent experience
Minimum 2 years' experience in the clinical research industry
Proficient with Microsoft Office and web-based applications
Highly detail-oriented and organized
Able to work independently and collaboratively within a team
Creation Specialist • Lubbock, Texas, United States