drjobs Supply Chain Lead (Secondment - 12-18 Months)

Supply Chain Lead (Secondment - 12-18 Months)

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1 Vacancy
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Job Location drjobs

New York City, NY - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Why Patients Need You

As a Supply Chain Lead (SCL) your advanced knowledge and solid understanding of clinical study design and drug supply processes you will lead and manage matrix teams responsible for the endtoend oversight of supply chain activities required for the provision of investigational product on phase IIV protocols for both Small Molecule and Biologics programs. You will also provide consultation on all aspects of investigational product strategies and a key decision maker for the development of investigational product supply and sourcing strategies. You are responsible for designing strategies that align with program protocol and regulatory requirements identifying and managing supply chain risk managing multimillion clinical supply budgets and providing guidance and leadership to the Clinical Supply Team (CST).

What You Will Achieve

The SCL will oversee the endtoend activities and identify potential risks and develop supply strategies that balance cost timelines and risks to support the development of candidates in the Pfizer Research & Development teams across the multiple business units within Pfizer.

The SCL is accountable for Pfizer clinical supplies delivery and oversight of endtoend process from API to finished product delivery to clinical sites. This role requires a thorough understanding of processes production cycle times strategies challenges risks and constraints of all Medicinal Sciences (MedSci) supply chain functions.

The SCL is the key Global Clinical Supply (GCS) point of contact for clinical study teams CoDevelopment Teams (CDTs) asset teams and Clinical Research Organizations (CROs) and represents GCS and MedSci functional lines at the core study team. The SCL provides study teams with innovative solutions to clinical drug supply production packaging labeling and distribution in order to influence clinical study design and drive successful execution.

The SCL is the matrix team lead of the MedSci GCS Clinical Supplies Team (CST) and provides broad consultation on all aspects of clinical drug supply.

How You Will Achieve It

  • Responsible for leading the development and execution of investigational and commercial material global supply strategies for early and latestage development programs intended for regulatory approvals of new products new indications or line extensions of currently approved products.

  • Participate as a key member of the Pharmaceutical Sciences Project Team (PSPTI and Co Development Team (CDT) to proactively recognize and address logistical and regulatory issues associated with the requirements of the clinical development program and project team objectives.

  • Participate as a core study team member to provide operational knowledge relating to lnvestigational Product (IP) and lead strategy discussions.

  • Proactively anticipate changes based on operational factors (countries sites enrollment) randomization configuration and protocol requirements.

  • In partnership with the CST develop clinical supply solutions including packaging blinding and distribution strategies that meet the needs of clinical studies as well as ensure patient compliance and safety.

  • Proactively identify risks and develop strategies to mitigate these risks and create contingency plans that minimize the impact of unanticipated events.

  • Manage clinical trial drug supply budget and communicate forecasts and changes effectively and in a timely fashion to study teams and GCS partner lines.

  • Maintain project information in GCS project tracking systems and in PharmSci project management systems.

  • Ensure site and patient focus along with quality compliance throughout PharmSci and GCS processes.

  • Act as a point of contact for clinical supply required input during audits and regulatory inspections as well as participate in inspection readiness activities.

  • Participate on Limited Duration Teams and Continuous Improvement projects.

Matrix Team Leadership:

As the matrix team lead of the CST the SCL will manage a network of internal and external partners to ensure GCS meets the customer expectations and supports the key Pfizer clinical study milestones and patient supply needs.

Establish and maintain behavioral norms and performance expectations for the CST.

Qualifications

MustHave

  • Bachelors Degree with 8 years of demonstrated and relevant experience in pharma/biotech project management and cross functional team leadership; clinical supply project management experience.

  • Demonstrated ability to manage large and complexclinical development programs.

  • Demonstrated capability to lead business development activities and acquisitions as they relate to clinical programs.

  • Demonstrated knowledge and experience working in a Good Manufacturing Practices (GMP) (cGMP) and Good Clinical Practices (GCP) (GxP) environment.

  • Demonstrated understanding of pharma quality and regulatory framework.

  • Demonstrated indepth experience managing multiple clinical studies in parallel.

  • Demonstrated experience leading and delivering in a matrix team environment.

  • Demonstrated electronic written and verbal communication skills.

  • Demonstrated breath 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 colleagues to achieve meaningful outcomes and create business impact.

  • Demonstrated understanding of latestage clinical drug development processes.

  • Demonstrated ability to inspire teams to deliver in a dynamic business environment through effective change management and leadership.

  • Demonstrated ability to develop and maintain clinical supply demand forecast and budgets.

NicetoHave

  • Relevant pharmaceutical experience.

  • Relevant operational experience across diverse business portfolio. e.g. Biopharmaceuticals Consumer Products other industries

  • Past oral presentations at conferences and other large audiences.

  • 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.

NONSTANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Limited travel for training meetings as required.


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.

PHYSICAL/MENTAL REQUIREMENTS

None

NONSTANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

None

Other Job Details

  • Last Date to Apply for Job:May 13 2025

  • Additional Location Information:NY Headquarters

  • Eligible for Relocation Package NO

  • Secondment 1218 months

  • If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the nondriving secondment. Please refer to the Fleet Policy and Procedures document for more information.

  • There will be no change to your current work location.

  • Position is considered Flexible and colleagues are expected to comply with Log In For Your Day(LIFYD) requirements at site location (e.g. about 2.5 days a week in office).

  • Note: This secondment offers a valuable opportunity for professional growth. It will need to be funded by the secondees home market.


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 EVerify employer. This position requires permanent work authorization in the United States.

Logistics & Supply Chain Mgmt

Employment Type

Full-Time

Company Industry

About Company

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