Associate Director - Regulatory Project Management

Employer Industry: Life Sciences Regulatory Affairs

• Salary up to $100/hr
• Opportunity for career advancement and growth within the organization
• Remote work opportunity with flexibility in working hours
• Engage in critical regulatory submission activities that impact the broader organization
• Work in a collaborative environment focused on achieving key project milestones
• Benefit from a supportive management structure with potential financial accountabilities

• Oversee complex project and portfolio plans from initiation to closeout
• Drive the definition of project milestones, tasks, deliverables, and resource requirements
• Lead strategies for risk mitigation and contingency planning within project plans
• Manage project status, issues, schedules, and accomplishments, communicating updates to stakeholders
• Supervise members of the submission management team and prepare necessary reports for resource discussions

• Bachelor’s degree in life sciences or a technology-related field
• Typically requires 10+ years of project management experience in regulatory/clinical project management or within a life sciences company
• Minimum of 2 years of supervisory/management experience
• Expertise in global regulatory filing project management and project management tools
• Excellent organization, communication, and stakeholder management skills

• Experience using Veeva Rim for content plan submissions
• Comprehensive understanding of global health authority submissions and guidelines
• Proven ability to adapt quickly to changing requirements and priorities
• Strong attention to detail and ability to persuade management to take action
• Experience balancing multiple tasks to meet priorities and timelines

#Life Sciences #Regulatory Affairs #Project Management #Remote Work #Career Opportunity

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