Gilead Sciences, Inc.
Manager, Global Clinical Supply Chain
Gilead Sciences, Inc., Foster City, California, United States, 94420
Manager, Global Clinical Supply ChainLocations: United States - California - Foster City
Time Type: Full time
Posted on: Vor 3 Tagen ausgeschrieben
Job Requisition ID: R0041903
Job Description
Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development.
Manager, Global Clinical Supply Chain
KEY RESPONSIBILITIES:
Manager, Global Clinical Supply Chain is a leader that 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.
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).
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.
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.
Develops and implements depot and clinical site seeding and resupply strategies.
Carries out operational/logistics strategies and works with Quality Assurance and other functional groups to execute strategies that ensure on-time and safe delivery of all clinical shipments.
Collaborates with Logistics management and other members of GCSC, PDM, and external partners to resolve shipping-related issues.
Supports the clinical development and PDM strategies working collaboratively within GCSC, Quality, and other functional groups to develop clinical supply strategies.
Ensures accurate inventory and records at depots through timely reconciliation.
Keeps abreast of clinical supply incidents and issues.
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).
Responsible for maintaining GDP, GMP, and global trade compliance.
Obtains and reviews quotes, approves purchase requisitions and invoices.
BASIC QUALIFICATIONS:
Bachelor’s degree with 7+ years of industry experience OR Master’s degree with 5+ years of experience OR PhD or PharmD degree with 0+ years of experience.
PREFERRED QUALIFICATIONS:
Degrees in the sciences preferred.
Strong working knowledge and experience in clinical supply management.
Working knowledge of clinical study designs, blinding practices, global trials.
Experience with managing comparator drugs and other co-meds for clinical studies.
Excellent verbal, written, and interpersonal communication skills.
Strong computer skills (e.g., email, word processing, spreadsheet creation and management).
Ability to manage the resources and timelines for complex clinical study and programs.
The salary range for this position is: $133,280.00 - $172,480.00. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package.
For additional benefits information, visit:
Gilead Benefits
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 other non-job related characteristics.
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Time Type: Full time
Posted on: Vor 3 Tagen ausgeschrieben
Job Requisition ID: R0041903
Job Description
Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development.
Manager, Global Clinical Supply Chain
KEY RESPONSIBILITIES:
Manager, Global Clinical Supply Chain is a leader that 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.
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).
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.
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.
Develops and implements depot and clinical site seeding and resupply strategies.
Carries out operational/logistics strategies and works with Quality Assurance and other functional groups to execute strategies that ensure on-time and safe delivery of all clinical shipments.
Collaborates with Logistics management and other members of GCSC, PDM, and external partners to resolve shipping-related issues.
Supports the clinical development and PDM strategies working collaboratively within GCSC, Quality, and other functional groups to develop clinical supply strategies.
Ensures accurate inventory and records at depots through timely reconciliation.
Keeps abreast of clinical supply incidents and issues.
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).
Responsible for maintaining GDP, GMP, and global trade compliance.
Obtains and reviews quotes, approves purchase requisitions and invoices.
BASIC QUALIFICATIONS:
Bachelor’s degree with 7+ years of industry experience OR Master’s degree with 5+ years of experience OR PhD or PharmD degree with 0+ years of experience.
PREFERRED QUALIFICATIONS:
Degrees in the sciences preferred.
Strong working knowledge and experience in clinical supply management.
Working knowledge of clinical study designs, blinding practices, global trials.
Experience with managing comparator drugs and other co-meds for clinical studies.
Excellent verbal, written, and interpersonal communication skills.
Strong computer skills (e.g., email, word processing, spreadsheet creation and management).
Ability to manage the resources and timelines for complex clinical study and programs.
The salary range for this position is: $133,280.00 - $172,480.00. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package.
For additional benefits information, visit:
Gilead Benefits
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 other non-job related characteristics.
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