Senior Manager, Regulatory Strategic Planning

DescriptionAbbVie is dedicated to discovering and delivering innovative medicines that address serious health issues today and tackle the medical challenges of tomorrow. The Senior Manager, Regulatory Strategic Planning, will oversee project management capabilities for cross-functional teams working within the Regulatory Affairs organization. This role combines scientific knowledge, regulatory, and business processes to effectively execute AbbVie’s regulatory strategies. The primary focus is on developing and managing schedules, activities, and deliverables for the Global Regulatory Product Teams (GRPTs) while driving process improvements for regulatory compliance and productivity.Compensation and Benefits• Competitive salary based on experience• Comprehensive benefits package including:• Paid time off (vacation, holidays, sick)• Medical, dental, and vision insurance• 401(k) plan• Eligibility for short-term and long-term incentive programsWhy you should apply for this position todayThis is an exciting opportunity to join a leading organization in the biopharmaceutical industry, where you will contribute to impactful projects that improve patient outcomes. You will work in a collaborative environment with talented professionals who are committed to innovation and making a difference in healthcare.Skills• Proficient knowledge of the regulatory product lifecycle and business processes• Strong leadership and project management capabilities• Effective problem-solving and decision-making skills• Excellent verbal and written communication skills• Ability to interact effectively with senior management and executivesResponsibilities• Provide project management leadership for GRPTs, ensuring regulatory milestones are tracked and achieved• Facilitate GRPT and related meetings, managing action items and summarizing highlights for stakeholders• Communicate regulatory milestones and updates with key stakeholders across the enterprise• Drive GRPT operations in support of the Global Regulatory Lead (GRL)• Plan and execute process improvement initiatives of medium to high complexity• Develop effective working relationships with project team members• Prepare and deliver clear written reports and presentations for various audiences• Coordinate deliverable preparation and manage budgets, contracts, and reporting processes• Analyze business performance metrics to drive compliance, quality, and productivity improvementsQualifications• Bachelor’s degree in science, math, engineering, business management, or a medical field• Advanced degree is preferred (e.g., Master’s, PhD)• Certifications such as RAC or PMP are preferred• 7 years’ related experience in a complex and matrix environment• Proven leadership skills and presenceEducation Requirements• Bachelor’s degree in relevant fields (biology, chemistry, engineering, etc.)• Advanced degree preferredEducation Requirements Credential Category• Science, Engineering, Business Management, or Medical FieldExperience Requirements• Minimum of 7 years of related experience• Demonstrated experience in leading teams and managing complex projects• Background in regulatory affairs or a related discipline is advantageousWhy work in North Chicago, ILNorth Chicago offers a vibrant community with a rich history and access to a range of cultural and recreational activities. The city is home to a robust health care and biopharmaceutical sector, providing numerous professional development opportunities. Residents enjoy beautiful parks, diverse dining options, and a welcoming atmosphere, making it an ideal place for both personal and professional growth.