Manager, Regulatory Program Management & Submission Strategy (Oncology)

Pfizer

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profile Job Location:

La Jolla, CA - USA

profile Monthly Salary: $ 99200 - 160500
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

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.

The annual base salary for this position ranges from $99200.00 to $160500.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.

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.

Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing please email. This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and/or interviewing. Requests for any other reason will not be returned.

Medical


Required Experience:

Manager

JOB SUMMARYThe 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 coordinati...
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Key Skills

  • Marketing
  • Data Visualization
  • Tableau
  • Customer Segmentation
  • Microsoft Powerpoint
  • Investment Banking
  • Strategic Planning
  • Financial Modeling
  • Customer relationship management
  • Management Consulting
  • Google Suite
  • Analytics

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