Senior Associate - Global Regulatory Operations Quality Review

November 15

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Description

β€’ Serves as primary contact for project scheduling β€’ Ensures timely resourcing of projects β€’ Collaborates on resourcing strategy β€’ Participates in automation of resourcing processes β€’ Manages contractor onboarding/outboarding β€’ Reviews vendor invoices for accuracy

Requirements

β€’ Understanding of the drug development process and regulatory document landscape β€’ Experience with clinical regulatory documents is preferred β€’ Technical data review or scientific review experience in biotech or pharma preferred β€’ Responsive and diplomatic communication skills β€’ Ability to prioritize competing tasks β€’ Microsoft Office proficiency

Benefits

β€’ Medical, dental, vision, and life insurance plans β€’ Flexible work options β€’ Exceptional support for family and the individual β€’ Discretionary annual bonus β€’ Discretionary stock-based long-term incentives β€’ Paid time off

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