Clinical Document Management Specialist IV

Clinical Document Management Specialist IV will manage and oversee Trial Master File (TMF) records from set-up through to final archival of the clinical trial, ensuring compliance with company SOPs and processes, and all applicable regulations.

Requirements

• Minimum 2 years of pharmaceutical industry experience
• Records management/TMF experience
• Familiarity with various aspects of clinical trials and regulatory submissions
• Current awareness of regulatory requirements for clinical trials (ICH/GCP)

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship
• Four Day Work Week
• Generous Parental Leave
• Tuition Reimbursement
• Relocation Assistance