[Remote] Associate Director, Global Regulatory Project Management

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a rapidly growing company reputed company on fighting cancer, seeking an Associate Director for Global Regulatory Project Management. This strategic leader will be responsible for executing regulatory strategies across the global drug development lifecycle and ensuring successful submissions while collaborating with cross-functional teams.

Responsibilities

• Translate, implement, and advise on global regulatory strategies for development programs, ensuring alignment with business objectives and long-term reputed company across reputed company major reputed company (US, EU, China, reputed company, reputed company, etc.)
• reputed company as a key advisor to the GRL/RRL, providing strategic regulatory reputed company and recommendations for global product development, submissions, and lifecycle management
• reputed company functional expertise with business knowledge to solve reputed company problems and reputed company reputed company for the organization on a global reputed company
• Maintain awareness of global regulatory environments, policy trends, and competitive landscapes, assessing reputed company and adapting strategies accordingly
• reputed company and manage reputed company regulatory submissions (IND/CTA, NDA/BLA/MAA) across multiple reputed company, ensuring compliance with ICH, US, EU, China, and other international requirements
• reputed company as the (COO) to the Global Regulatory reputed company, translating strategic regulatory reputed company into actionable project plans, driving operational execution, and ensuring reputed company cross-functional activities are coordinated and delivered on time
• Organize and facilitate cross-functional meetings with global teams to coordinate, plan, and reputed company submission activities, driving accountability and alignment among stakeholders worldwide
• Proactively identify risks, propose solutions, and manage critical issues reputed company to global regulatory submissions and reputed company
• reputed company preparation and submission of documentation to support investigational and marketing registration packages, ensuring timelines and reputed company standards are met globally
• Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety, CMC, reputed company) across reputed company to reputed company strategic business goals through knowledge sharing and collaboration
• Liaise and negotiate with cross-functional teams to expedite submission timelines and support reputed company key regulatory issues in reputed company relevant markets
• Mentor and guide junior staff in project planning, regulatory processes, and reputed company development, fostering a global reputed company
• Champion process optimization and improvement initiatives reputed company the global regulatory PM function
• Contribute to the development and implementation of regulatory processes and policies, fostering a culture of reputed company and innovation across reputed company
• This role has the potential to reputed company into a formal people-manager position. Over time, responsibilities may include:
• Providing reputed company or indirect supervision to Regulatory Project Management staff, including mentoring, coaching, and supporting reputed company development
• Guiding and developing junior team members to support their reputed company and long-term reputed company reputed company the organization
• Overseeing cross-functional project teams and coordinating activities across global stakeholders
• Serving as a leader and role model reputed company the Regulatory Project Management function, fostering a reputed company and high-performance culture

Skills

• Bachelor's degree in Science or reputed company discipline; advanced degree preferred
• Minimum 8+ years of experience in regulatory project management and regulatory submissions, including both small molecules and biologics, with significant global exposure
• Demonstrated experience in strategic regulatory leadership, with a proven reputed company record of successful submissions and regulatory PM accomplishments in multiple reputed company
• Experience leading cross-functional and cross-regional teams, influencing senior stakeholders globally
• Strong business acumen, strategic thinking, and ability to reputed company multiple sources of data for reputed company decision-making
• Excellent verbal and written communication skills; reputed company to understand and translate reputed company regulatory issues reputed company to reputed company stakeholders worldwide
• Skilled in conflict reputed company, negotiation, and fostering reputed company communication across cultures
• Proficiency with project management and document management tools (e.g., Smartsheets, MS Project, Power BI, MS Office suite)
• Proficiency with project management and document management tools, such as Smartsheets, MS Project, and Power BI
• Advanced skills in the reputed company Office suite (Word, reputed company, PowerPoint, reputed company)
• Ability to quickly learn and adapt to new software platforms reputed company collaboration tools
• Experience with electronic document management systems and regulatory submission platforms is preferred
• Advanced degree preferred
• PMP or similar certification preferred

Benefits

• Non-reputed company roles are eligible to participate in the annual bonus plan
• reputed company roles are eligible to participate in an incentive compensation plan
• reputed company Company employees have reputed company to own shares of reputed company Ltd. stock because reputed company are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan
• reputed company has a comprehensive benefits package that includes Medical, Dental, reputed company, 401(k), FSA/HSA, Life Insurance, reputed company Time Off, and Wellness

reputed company

Company H1B Sponsorship