Associate Regulatory Writing

Amgen is seeking an Associate Regulatory Writing professional to prepare clinical regulatory documents for public disclosure, collaborate with team members, and manage timelines.

Requirements

• Prepare clinical regulatory documents for public disclosure
• Collaborate with team members to resolve problems and escalate issues
• Manage timelines and coordinate work across team
• Execute clinical trial disclosure business process
• Assist/support trial disclosure audits and inspections
• Serve as Process Administer for CTRS