Director, Sample Logistics, Vaccines R&D

Pfizer

Pearl River, Northern (NY, KY)

On-site

USD 177,000 - 294,000

Full time

14 days+
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Benefits offered by this job

401(k) with Pfizer matching
Health, dental & vision insurance
Paid vacation, holidays & personalDays
Relocation assistance
Pfizer Retirement Savings Contribution

Job summary

Pfizer in Pearl River, NY is seeking a leader to manage the clinical sample logistics function for its vaccine portfolio, overseeing end-to-end operations from study start-up to disposition. You will lead a 40+ team, drive global strategies, ensure sample integrity, regulatory compliance, and partner with cross-functional teams to support vaccine programs.

The role emphasizes digital and automation innovations, vendor governance, and scalable processes to enable successful clinical trials.

Qualifications

  • Bachelor's degree in a related field; 8+ years of logistics or biopharma experience.
  • 5+ years of direct people management leadership of large teams.
  • Experience in regulated environments with quality and risk management.
  • Strong written and verbal communication for senior leadership.

Responsibilities

  • Lead a global sample logistics function with 40+ colleagues worldwide.
  • Develop scalable operating models, governance, and business continuity plans.
  • Ensure sample integrity and regulatory compliance across temp-controlled shipments.
  • Drive automation, dashboards, and AI-enabled capabilities for visibility.
  • Partner with cross-functional teams and external vendors.

Skills

Team leadership
Regulatory compliance
Strategic planning
Cross-functional collaboration
Effective communication
Project management

Education

Bachelor's degree in Supply Chain Management, Life Sciences, Biotechnology, or related

Job description

POSITION SUMMARY You will be responsible for managing the clinical sample logistics function for Pfizer's vaccine clinical portfolio, ensuring samples are transported safely, compliantly, and reliably across domestic and international clinical trial networks to the Pearl River, NY biorepository and then distributed to our network of internal and external testing laboratories. You will lead an end-to-end logistics strategy from study start-up through operations and finally sample disposition. Your responsibilities include leading a large team, improving global logistics capabilities, advancing digital and automation initiatives, and partnering with Vaccines, Quality, Legal, Finance, Compliance, clinical study teams, couriers, and technology vendors. You will be accountable for maintaining sample integrity, enabling global clinical trial execution, and developing scalable logistics processes to support Pfizer's vaccine pipeline.

KEY RESPONSIBILITIES

Lead the global sample logistics function--Provide strategic and operational leadership for a team of 40+ colleagues responsible for domestic and international shipment execution, study start-up support, ongoing operations, and clinical sample lifecycle management. Shape long-term sample logistics strategy. Develop scalable operating models, governance frameworks, and business continuity plans that support pipeline growth, clinical trial expansion, and evolving global regulatory expectations. Protect sample integrity and compliance. Ensure reliable, temperature-controlled movement of clinical biological samples while maintaining adherence to applicable FDA, EMA, IATA, DOT, CDC, trade compliance, GCLP, and Pfizer quality requirements. Advance inspection readiness and quality oversight. Maintain robust documentation and audit-ready processes for deviation management, CAPAs, change controls, and training across sample logistics activities. Drive vendor governance and external partnership performance. Own courier and technology partner governance, service expectations, escalation pathways, performance metrics, contracts, and continuous improvement initiatives. Modernize operations through digital and automation innovation. Lead automation, robotics, dashboarding, track-and-trace, predictive planning, AI-enabled sample management, and performance analytics initiatives that improve visibility, decision-making, compliance, and efficiency. Partner across the enterprise. Serve as a Vaccines representative and subject matter expert in cross-functional forums involving clinical assay teams, study management, Quality, Legal, Finance, Trade Compliance, Research Informatics, Project Management, Data Management, and external partners. Develop people and culture. Lead workforce planning, talent acquisition, performance management, career development, and succession planning while fostering high morale, collaboration, accountability, continuous learning, and open communication. Communicate with executive impact. Present complex logistics data, risk profiles, investment needs, and operational improvement opportunities clearly to senior leaders and cross-functional decision-makers.

QUALIFICATIONS MUST HAVE

Bachelor's degree in Supply Chain Management, Life Sciences, Biotechnology, or a related discipline. 8+ years of logistics, supply chain, clinical trial operations, central laboratory, or biopharmaceutical experience. 5+ years of direct people management experience, including successful leadership of large teams or multi-tiered management structures. Experience leading in a regulated environment and making sound judgments to complex operational, quality, compliance, and risk-management decisions. Knowledge of global sample logistics, cold-chain management, temperature-controlled shipping, customs requirements, infectious substance transport, and biohazard shipping regulations. Proven success building relationships, influencing without direct authority, negotiating with internal and external stakeholders, and leading through matrixed teams. Excellent verbal and written communication skills, including the ability to translate complex operational information into clear recommendations for senior leadership. Strong change agility, problem-solving skills, and experience managing competing priorities in a fast-paced environment.

NICE TO HAVE

Advanced degree in Supply Chain Management, Life Sciences, Biotechnology, Business Administration, or a related discipline. Experience working in a GCLP, GLP, GMP, clinical trial, vaccine, central laboratory, or regulated sample management environment. Experience leading automation, robotics, digital tools, dashboards, AI-enabled capabilities, or analytics initiatives in clinical operations, logistics, laboratory, or supply chain settings. Experience overseeing external vendors, couriers, technology partners, contracts, service levels, and supplier performance improvement. Experience defining and leading complex programs, executing with quality and timeliness, and delivering measurable business impact. The ideal candidate brings a breadth of leadership experience and the ability to inspire teams, develop talent, influence peers, simplify complexity, and create meaningful business impact. This leader will be energized by building high-performing operations, strengthening quality systems, introducing new technologies, and enabling vaccine programs that have the potential to improve lives around the world.

PHYSICAL/MENTAL REQUIREMENTS

Ability to perform work while sitting or standing and to operate effectively in a complex, highly regulated, and deadline-driven environment.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

This position may require occasional evening or weekend work to support critical business timelines, global shipment needs, or issue escalation. Occasional travel may be required for Pfizer site visits, courier or CRO interactions, scientific meetings, inspections, or other business needs. Relocation support available

WORK LOCATION ASSIGNMENT:

The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 20.0% 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 life's 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 | (uscandidates.mypfizerbenefits.com). 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. Candidates must be authorized to be employed in the U.S. by any employer. U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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 www.pfizer.com/careers accessible 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 disabilityrecruitment@pfizer.com. 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. To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Research and Development

Pfizer 职业生涯与众不同。在我们的主人翁文化中,我们相信我们能够让医疗保健行业未来更美好,我们有潜力改善数以百万计人的生活。我们正在寻找新人才,加入我们的全球人才队伍,开发创新疗法,让世界变得更健康。

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