Why Patients Need You
At Pfizer, our mission is to inspire a best-in-class culture of continuous improvement and project management that empowers colleagues and enables simple, effective processes. Whether you are managing projects or liaising with others, your contribution in this team will help in making our work easier and faster so that we can deliver breakthroughs that change patients' lives.
Position Summary
You will oversee and manage operational aspects of ongoing regulatory oncology projects, acting as a liaison between the project teams and the line management. You will support our programs by managing the status review of the project, budget, schedules and preparing reports. You will develop mechanisms for monitoring project progress and for intervention and problem solving with project managers, line managers, and clients. You will assess project issues and develop resolutions to meet productivity, quality and client satisfactions goals.
You will lead complex projects across the division, including anticipating and troubleshooting roadblocks and influencing teams to achieve targets for the division.
Key Responsibilities
Develop ideas, manage plans to achieve objectives and lead or co-lead projects across the division.
Facilitate the development, implementation and management of business strategies.
Manage the development of the project plan with cross functional teams to deliver the program on time, within schedule, and within budget.
Develop and execute communication plan to ensure effective and timely communication between the core Team and functional management, senior management, and external partners.
Prepare periodic management and progress reports.
Promote a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity.
Provide project information necessary to support portfolio-level decision making and prioritization.
Coordinate and ensure long-range needs for expansion of production equipment, identify novel upstream and downstream processes and assimilate them into the relevant work streams.
Capitalize on the foundation of knowledge in the areas of Pfizer historic study performance data, competitor trial performance, real world data, and industry benchmarks using a variety of analytic and modeling tools.
Monitors team performance and proactively alerts team and management about deviations from plan.
Qualifications
Must-Have
Bachelor's Degree
7+ years of experience leading projects in a highly regulated environment
Cross-functional project management experience
Knowledge of drug development including a thorough understanding of the processes associated with feasibility, clinical study start-up and business operations
Outstanding project management and organizational skills
Excellent presentation and communication skills
Experience successfully managing multiple projects with multiple deadlines
Knowledge of the pharmaceutical manufacturing and associated processes
Experience in a Pharmaceutical Good Manufacturing Practices/cGMP environment
Familiarity with Pharmaceutical Sciences infrastructure
Nice-to-Have
Experience with product development processes within a pharmaceutical or medical device company
Oncology experience preferred
Familiarity with clinical trial execution, working with contract research organizations, budget management, and related areas
Experience leading regulatory submissions for drug applications
Experience with Microsoft Project, Planisware, and/or OnePage
Project Management Professional (PMP) certification
PHYSICAL/MENTAL REQUIREMENTS
Lifting, sitting, standing, walking, bending, ability to perform critical thinking.
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 provider’s 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.
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