Senior Associate - Global Regulatory Operations Quality Review
2 days ago
Description
• Serves as primary contact for project scheduling • Ensures timely resourcing of projects • Collaborates on resourcing strategy • Participates in automation of resourcing processes • Manages contractor onboarding/outboarding • Reviews vendor invoices for accuracy
Requirements
• Understanding of the drug development process and regulatory document landscape • Experience with clinical regulatory documents is preferred • Technical data review or scientific review experience in biotech or pharma preferred • Responsive and diplomatic communication skills • Ability to prioritize competing tasks • Microsoft Office proficiency
Benefits
• Medical, dental, vision, and life insurance plans • Flexible work options • Exceptional support for family and the individual • Discretionary annual bonus • Discretionary stock-based long-term incentives • Paid time off
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💰 $101M Private Equity Round on 2004-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance