Senior Manager, Global Clinical Supply Chain

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At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe.

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Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations.

Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

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As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations.

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Job Description

Senior Manager, Global Clinical Supply Chain

KEY RESPONSIBILITIES :

Senior Manager, Global Clinical Supply Chain is a leader that who carries out leadership vision and directions while providing expertise for Gilead's global

clinical trials. Works collaboratively within the department and with cross functional colleagues (e.g., Regulatory, Clinical Operations, Quality, PDM sub-

teams, GSC, etc.) to develop strategies, meet project deliverables, and solve business problems. The position has end-to-end leadership and accountability

for clinical supply management. Prioritizes and creates executable work plans to ensure on time in full, safe delivery of investigational medicinal products

IMP).

FOCUS AREAS :

Interprets clinical study protocols and / or dosing schema. Translates the information to IMP demand and supply planning requirements, distribution

strategies including depot inventory management.

Performs demand and / or supply forecasting and planning with planning horizon of 9 to 18 months. Translate forecasts into clinical packaging and

labeling (CPL) execution plans. Supports contract / quote reviews and purchase order and invoice reconciliations.

Develops and implements depot and clinical site seeding and resupply strategies.

Supports the clinical development and PDM strategies working collaboratively within GCSC, Quality and other functional groups to develop clinical

supply strategies and plan with the focus on delivering compliant, quality IMP to clinical trials globally on time in full.

Ensures accurate inventory and records at depots through timely reconciliation.

Keeps abreast of clinical supply incidents and issues. Reports and escalates issues as well as investigates root cause as appropriate.

Performs tasks in Gilead systems (e.g., SAP, IVRS, QMS, etc.) to enable compliant and efficient progression of IMP through the supply chain.

Authors SOPs and business process work instructions as per leadership direction and support.

Supports regulatory filings and inspections.

Maintains compliance of clinical supply deliverables for clinical study reports (CSR) and trial master file (TMF).

Maintains compliance to required training.

Basic Qualification :

Bachelor’s degree with 8+ years of industry experience OR Master’s degree with 6+ years of experience OR PhD or PharmD degree with 2+ years of

experience.

The role may have people leadership accountabilities which include recruiting, onboarding, developing, retaining and managing staff.

Has mature working knowledge of supply chain and experience working with GxP environment. Has strong cross-functional, multi-cultural awareness and

communication skills in a fast-paced, global company

Preferred Qualifications :

Degrees in the sciences preferred.

Strong working knowledge in clinical supply management including and not limited to forecasting, demand / supply planning, IVRS and ERP

systems.

Working knowledge of clinical study designs, blinding practices, global trials, from Phase 1 first in human to late phase.

Working knowledge of Clinical Demand and Operations Planning (CD&OP).

Experience with managing comparator drugs and other co-meds for clinical studies.

Ability to collaborate, influence and negotiate to work effectively with cross-functional teams and external suppliers to meet clinical development

timelines and patient needs.

Works effectively with ambiguity. Ability to devise, assess and implement best options in alignment with Gilead's core values and functional

expectations.

Excellent verbal, written, and interpersonal communication skills. Ability to write clear and concise documents / presentations.

Strong computer skills (e.g., email, word processing, spreadsheet creation and management, online search, etc.). Ability to efficiently adopt systems

and databases used at Gilead.

The salary range for this position is : $154,020.00 - $199,320.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location.

These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.

Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit :

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States :

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws.

In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' () poster.

NOTICE : EMPLOYEE POLYGRAPH PROTECTION ACT ()

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION ()

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors :

Please log onto your Internal Career Site (!CK5mGhIKBggDEMenAhIICgYI1A0QtgI / cacheable-task / 2997$2151.htmld#backheader true) to apply for this job.

Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people.

The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer.

Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.