Manager, Regulatory Affairs coordinating global regulatory submissions for therapeutic development. Collaborating cross-functionally to meet regulatory agency requirements and ensure compliance.
Responsibilities
Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development
Assist in coordination and preparation for Agency meetings and associated briefing document preparation
Leads and tracks queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries
Provide periodic status updates regarding conditions/commitments
Provide representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings
Requirements
MD, PhD or PharmD degree
2+ years of regulatory experience
Good understanding of US FDA and international pharmaceutical guidance
Knowledge of drug development process and industry standard practices
Interaction with CROs in the management of ex-US/ex-EU CTAs preferred
Strong interpersonal skills both written and verbally
Ability to coordinate and prioritize assigned projects according to company goals
Benefits
Health and wellness programs (including medical, dental, vision, life, and disability insurance)
Fitness centers
401(k) company match
Family support benefits
Equity awards
Annual bonuses
Paid time off
Paid leaves (e.g., military and parental leave) for eligible employees at all levels!
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