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A leading company in the pharmaceutical industry is looking for a Program Manager to support Vaccine product development. This role involves project management, cross-functional team coordination, and strategic alignment to ensure timely development and delivery of vaccines. Ideal candidates will have a strong pharmaceutical background, proven leadership skills, and the ability to navigate complex interpersonal dynamics.
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
ROLE SUMMARY
Supports the Program Director in providing overall project management for Vaccine product development teams to develop new vaccines from Research through product registration, ensuring alignment of strategic and operational objectives.
Possesses a comprehensive knowledge of vaccine/drug development, resource management concepts, associated business processes, and project planning software and applies skills and general vaccine/drug development knowledge to contribute to the achievement of team or department goals.
Typically works within a cross-functional team environment and may lead/co-lead moderately complex sub-team initiatives.
Plays a key supportive role in scenario planning, supports several clinical or regulatory workstreams/ timelines within a program.
Will lead/co-lead/drive cross-functional sub-teams to ensure that the deliverables of the program are on track and achieved.
Expected to have excellent interpersonal skills and use a variety of communication methods and reporting/analytical tools to communicate critical project information to partner lines and others to enable team, line and portfolio decision making.
ROLE RESPONSIBILITIES
Develop and lead complex projects, managing plans to achieve objectives.
Make decisions to resolve moderately complex problems.
Support Program Leaders and Directors in creating comprehensive program plans aligned with overall strategy for developing vaccines and therapeutics.
Ensure alignment among strategic, operational, and line plans.
Interact closely with scientific staff to address everyday facility challenges and manage large capital facility projects with a scientific perspective.
Apply technical, team, and scheduling expertise to contribute to team deliverables and translate strategic objectives into operational plans.
BASIC QUALIFICATIONS
BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience
Knowledge of project management tools
Proficiency in Microsoft Office Suite
Strong analytical and problem-solving skills
Ability to manage multiple projects simultaneously
Excellent communication skills, both written and verbal
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
PREFERRED QUALIFICATIONS
A Master’s degree (MA/MS/MBA) with 7+ years of experience or a Doctorate (PhD/PharmD/JD) with 4+ years of relevant experience
PMP or similar Project Management Certifications
Strong understanding of clinical operations protocols and site budgets
Ability to influence and lead
High emotional intelligence and ability to navigate complex interpersonal dynamics
Ability to adapt to changing priorities and work effectively under pressure
Relocation support available
Work Location Assignment:Hybrid
ROLE SUMMARY
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
ROLE SUMMARY
Supports the Program Director in providing overall project management for Vaccine product development teams to develop new vaccines from Research through product registration, ensuring alignment of strategic and operational objectives.
Possesses a comprehensive knowledge of vaccine/drug development, resource management concepts, associated business processes, and project planning software and applies skills and general vaccine/drug development knowledge to contribute to the achievement of team or department goals.
Typically works within a cross-functional team environment and may lead/co-lead moderately complex sub-team initiatives.
Plays a key supportive role in scenario planning, supports several clinical or regulatory workstreams/ timelines within a program.
Will lead/co-lead/drive cross-functional sub-teams to ensure that the deliverables of the program are on track and achieved.
Expected to have excellent interpersonal skills and use a variety of communication methods and reporting/analytical tools to communicate critical project information to partner lines and others to enable team, line and portfolio decision making.
ROLE RESPONSIBILITIES
Develop and lead complex projects, managing plans to achieve objectives.
Make decisions to resolve moderately complex problems.
Support Program Leaders and Directors in creating comprehensive program plans aligned with overall strategy for developing vaccines and therapeutics.
Ensure alignment among strategic, operational, and line plans.
Interact closely with scientific staff to address everyday facility challenges and manage large capital facility projects with a scientific perspective.
Apply technical, team, and scheduling expertise to contribute to team deliverables and translate strategic objectives into operational plans.
BASIC QUALIFICATIONS
BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience
Knowledge of project management tools
Proficiency in Microsoft Office Suite
Strong analytical and problem-solving skills
Ability to manage multiple projects simultaneously
Excellent communication skills, both written and verbal
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
PREFERRED QUALIFICATIONS
A Master’s degree (MA/MS/MBA) with 7+ years of experience or a Doctorate (PhD/PharmD/JD) with 4+ years of relevant experience
PMP or similar Project Management Certifications
Strong understanding of clinical operations protocols and site budgets
Ability to influence and lead
High emotional intelligence and ability to navigate complex interpersonal dynamics
Ability to adapt to changing priorities and work effectively under pressure
Relocation support available
Work Location Assignment:Hybrid
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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