A company is looking for a Source Creation Specialist to join their Quality department.
Key Responsibilities Create and maintain source documents while ensuring compliance with SOPs and regulations Participate in study-related meetings and manage source document reviews from End Users Track findings from source reviews and escalate critical issues 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 organized and self-motivated Adaptable and willing to take on additional responsibilities as needed