Gilead Sciences, Inc.
Executive Director, Global Clinical Supply Chain - Oncology
Gilead Sciences, Inc., Foster City, California, United States, 94420
Executive Director, Global Clinical Supply Chain - Oncology
United States - California - Foster CityJob DescriptionAt 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. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.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.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. 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 fulfill their aspirations. Join Gilead and help create possible, together.Executive Director, Global Clinical Supply Chain (GCSC)KEY RESPONSIBILITIES:Responsible for leading clinical planning function within an assigned therapeutic area (TA).Inspires and motivates teams while leading the overall strategy supporting the GCSC function.Provides subject expertise on a diverse portfolio of development programs and different therapeutic modalities including small molecules, biologics, and cell gene therapy for Gilead’s global clinical trials.Works internally with members in GCSC and other functions including Development Operations, Clinical Operations, and Process Development and Manufacturing (PDM) to develop strategies, meet project deliverables, solve business problems, and create competitive advantage.Includes end-to-end elements of clinical planning and execution from the protocol design through manufacturing to the ultimate distribution and inventory management of clinical supplies at clinical sites worldwide.FOCUS AREA:Establishes strategies to ensure uninterrupted clinical supply for the overall development portfolio, including clinical development programs and studies at all phases as well as managed access programs.Leads, develops, and manages team, including recruitment, onboarding, and succession planning.Drives excellence and accountability for setting clear goals and consistently delivering.Responsible for developing and maintaining a culture of continuous improvement.Champions clinical demand and operation planning (CD&OP) interfacing with leaders from Clinical Operations, PDM sub-teams.Ensures efficient and robust resource allocation for PDM sub-teams and clinical study teams.Partners across several PDM functions and with other enterprise functions to ensure the on-time delivery of investigational medicinal product (IMP).Responsible for decision-making and directing the long-term vision of optimal supply chain strategies including labeling and distribution activities.Responsible for planning SOPs, Work Instructions, business policies, and procedures to ensure GxP compliance.Oversees and supports clinical study planners.Responsible for the departmental budgeting process.Basic Qualifications:16+ Years of relevant industry experience with BA/BS. OR 14+ Years with MA/MS or MBA PHD or PharmD.Has an expert working knowledge of clinical supply chain best practices and experience working with a GxP environment.Demonstrates hands-on end-to-end clinical supply knowledge and experience with clinical trials in therapeutic area of oncology.Preferred Skills:Degree in a science-related field; MS, PharmD, or MBA desirable.Strong clinical supply management experience/knowledge.Prior experience in complex Oncology trials is highly-preferred.Excellent verbal, written, and interpersonal communication skills are required.Gilead Core Values• Integrity (Doing What’s Right)• Accountability (Taking Personal Responsibility)The salary range for this position is: $274,635.00 - $355,410.00.
#J-18808-Ljbffr
United States - California - Foster CityJob DescriptionAt 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. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.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.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. 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 fulfill their aspirations. Join Gilead and help create possible, together.Executive Director, Global Clinical Supply Chain (GCSC)KEY RESPONSIBILITIES:Responsible for leading clinical planning function within an assigned therapeutic area (TA).Inspires and motivates teams while leading the overall strategy supporting the GCSC function.Provides subject expertise on a diverse portfolio of development programs and different therapeutic modalities including small molecules, biologics, and cell gene therapy for Gilead’s global clinical trials.Works internally with members in GCSC and other functions including Development Operations, Clinical Operations, and Process Development and Manufacturing (PDM) to develop strategies, meet project deliverables, solve business problems, and create competitive advantage.Includes end-to-end elements of clinical planning and execution from the protocol design through manufacturing to the ultimate distribution and inventory management of clinical supplies at clinical sites worldwide.FOCUS AREA:Establishes strategies to ensure uninterrupted clinical supply for the overall development portfolio, including clinical development programs and studies at all phases as well as managed access programs.Leads, develops, and manages team, including recruitment, onboarding, and succession planning.Drives excellence and accountability for setting clear goals and consistently delivering.Responsible for developing and maintaining a culture of continuous improvement.Champions clinical demand and operation planning (CD&OP) interfacing with leaders from Clinical Operations, PDM sub-teams.Ensures efficient and robust resource allocation for PDM sub-teams and clinical study teams.Partners across several PDM functions and with other enterprise functions to ensure the on-time delivery of investigational medicinal product (IMP).Responsible for decision-making and directing the long-term vision of optimal supply chain strategies including labeling and distribution activities.Responsible for planning SOPs, Work Instructions, business policies, and procedures to ensure GxP compliance.Oversees and supports clinical study planners.Responsible for the departmental budgeting process.Basic Qualifications:16+ Years of relevant industry experience with BA/BS. OR 14+ Years with MA/MS or MBA PHD or PharmD.Has an expert working knowledge of clinical supply chain best practices and experience working with a GxP environment.Demonstrates hands-on end-to-end clinical supply knowledge and experience with clinical trials in therapeutic area of oncology.Preferred Skills:Degree in a science-related field; MS, PharmD, or MBA desirable.Strong clinical supply management experience/knowledge.Prior experience in complex Oncology trials is highly-preferred.Excellent verbal, written, and interpersonal communication skills are required.Gilead Core Values• Integrity (Doing What’s Right)• Accountability (Taking Personal Responsibility)The salary range for this position is: $274,635.00 - $355,410.00.
#J-18808-Ljbffr