JOB SUMMARY
The Manager Regulatory Program Management & Submission Strategy (RPMSS) provides comprehensive regulatory program management support that ensures alignment with and execution of Pfizer Oncologys regulatory strategies and submission deliverables. This position is accountable for coordination and prioritization of regulatory activities facilitation of decision-making processes and oversight of information flow to ensure adherence to regulatory timelines and commitments. The Manager RPMSS plays a critical role in partnering with regulatory strategists to advance regulatory and submission activities for assigned programs within the oncology portfolio.
JOB RESPONSIBILITIES
The Manager RPMSS will provide comprehensive support to Pfizer Oncologys Global Regulatory Strategy Teams (GRST) and Submission Teams ensuring efficient execution in accordance with program strategy. Responsibilities include but are not limited to:
Develop and manage submission timelines and milestones using appropriate tools. Identify efficiencies to enable fast filings and convert submission timelines into clear actionable tasks with proactive follow-up to ensure on-time delivery.
Contribute to the design and implementation of processes that enhance workflow efficiency and provide guidance on best practices and procedures.
Organize and manage GRST Submission Team MCI and other leadership pre-alignment meetings including scheduling agenda preparation material distribution minute-taking action item follow-up and appropriate storage of all documentation.
Proactively identify and resolve project issues to meet productivity quality and organizational goals.
Lead or co-lead projects effectively managing time and resources for oneself with consideration of impact on team members.
Develop and maintain templates dashboards team rosters document reviewer lists SharePoint/Teams sites and action trackers.
Independently prepare comprehensive status reports timelines tables graphs correspondence and presentations as needed for internal and external stakeholders.
Track and analyze metrics to support business insights.
Assist with onboarding of new team members and provide training and guidance for new project system users.
QUALIFICATIONS/SKILLS
Education
Bachelors Degree with 4 years of experience or Masters Degree with 2 years of experience
Experience
2-4 years of experience in the biopharmaceutical industry understanding of
Oncology preferred
Experienced in managing day-to-day planning and project management to enable execution of complex strategies
Experienced in communicating and interacting with senior executive stakeholders
Experienced in managing multiple competing tasks simultaneously
Demonstrated ability to work collaboratively with diverse teams and manage a
team of cross-functional colleagues
Demonstrated understanding of systems and structures and ability to implement efficient processes
Attributes
Demonstrate resourcefulness with proven ability to anticipate needs prioritize
responsibilities and manage multiple priorities with tight timelines
Strong project management skills with demonstrated attention to detail
Possess a high energy level sense of urgency creativity decisiveness ability to work hard under pressure
Demonstrated strong self-starter independent proactive solutions oriented and self-motivated
Ability to exhibit sound judgment in handling confidential information
Ability to work well both in team environment as well as operate independently
with limited direct supervision
Possess excellent communication skills with an ability to respond with
professionalism in verbal and written communications with all levels of the
organization
Proficiency in MS Word Excel PowerPoint and Outlook are essential;
understanding of MS Project is preferred
Know and model Pfizer Values and Pfizer Core Competencies
Excellent collaborator and ability to navigate a fast-paced highly matrixed
environment
Work Location Assignment:Hybrid - must be onsite an average of 2.5 days per week.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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Required Experience:
Manager
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