Corbus Pharmaceuticals, Inc.
Associate Director, Clinical Supply Chain
Corbus Pharmaceuticals, Inc., Oklahoma City, Oklahoma, United States,
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Associate Director, Clinical Supply Chain
Associate Director, Clinical Supply Chain Remote Worker - N/A, GBR Our passion. Our purpose. At Corbus, it starts at our core. We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow. At Corbus, transformative ideas can come from anyone, anywhere and anytime. We offer our team flexibility and the opportunity to excel in their professional journey. We provide a welcoming space where collaboration, mentorship and diversity are encouraged. We come together, like no other, to elevate each other and focus on what’s best for patients. About Corbus Corbus is a precision oncology company with a diversified portfolio and is committed to helping people defeat serious illness by bringing innovative scientific approaches to well-understood biological pathways. Our pipeline is comprised of two experimental drugs targeting solid tumors: CRB-701, a next-generation antibody drug conjugate (“ADC”) that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload and CRB-601, an anti-integrin monoclonal antibody that blocks the activation of TGFß expressed on cancer cells. The pipeline also includes CRB-913, a highly peripherally restricted cannabinoid type-1 (“CB1”) receptor inverse agonist for the treatment of obesity. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on Twitter, LinkedIn and Facebook. Corbus Pharmaceuticals Holdings, Inc. is an equal opportunity employer. Job Description We seek a clinical supply chain professional experienced in overseeing contract manufacturing, packaging and labeling operations and clinical supply chain management to help build and grow our planning and scheduling functions. You will work closely with internal teams and external partners to ensure materials are available to meet manufacturing, testing, and clinical trial objectives and to develop executable production plans and schedules. This position will report to the head of CMC. This role will be based remote in the United Kingdom. PRIMARY RESPONSIBILITIES: Overall responsibility for the labelling, packaging and distribution of Corbus clinical supplies. Oversight of inventory at warehouses and distribution facilities. Collaborate with CMC and Clinical Operations to develop material lot use strategies. Creation and maintenance of demand forecasts at a study, country and site level, in collaboration with clinical operations. Collaborate with Quality Assurance to ensure and maintain vendor qualification. Importation and customs management for clinical supplies. Working with partners to manage comparators and auxiliary supplies. Work with Global Regulatory Affairs, QPs, Quality Assurance and other stakeholders to ensure timely release of supplies. IRT CMC Management. Requirements: Minimum of a bachelor’s degree or equivalent experience. Min 5 years in a related supply chain role at a biotech or pharmaceutical company. Experience with managing investigational supplies for blinded and open label studies. Proficiency with IWRS/IVRS. APICS CPIM or CSCP Certification preferred. Experience managing schedules and priorities. Experience with cGMP operations is preferred. Proficiency in use of MS Excel, Project and other applications. Excellent interpersonal, verbal and written communication skills.
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Associate Director, Clinical Supply Chain
Associate Director, Clinical Supply Chain Remote Worker - N/A, GBR Our passion. Our purpose. At Corbus, it starts at our core. We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow. At Corbus, transformative ideas can come from anyone, anywhere and anytime. We offer our team flexibility and the opportunity to excel in their professional journey. We provide a welcoming space where collaboration, mentorship and diversity are encouraged. We come together, like no other, to elevate each other and focus on what’s best for patients. About Corbus Corbus is a precision oncology company with a diversified portfolio and is committed to helping people defeat serious illness by bringing innovative scientific approaches to well-understood biological pathways. Our pipeline is comprised of two experimental drugs targeting solid tumors: CRB-701, a next-generation antibody drug conjugate (“ADC”) that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload and CRB-601, an anti-integrin monoclonal antibody that blocks the activation of TGFß expressed on cancer cells. The pipeline also includes CRB-913, a highly peripherally restricted cannabinoid type-1 (“CB1”) receptor inverse agonist for the treatment of obesity. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on Twitter, LinkedIn and Facebook. Corbus Pharmaceuticals Holdings, Inc. is an equal opportunity employer. Job Description We seek a clinical supply chain professional experienced in overseeing contract manufacturing, packaging and labeling operations and clinical supply chain management to help build and grow our planning and scheduling functions. You will work closely with internal teams and external partners to ensure materials are available to meet manufacturing, testing, and clinical trial objectives and to develop executable production plans and schedules. This position will report to the head of CMC. This role will be based remote in the United Kingdom. PRIMARY RESPONSIBILITIES: Overall responsibility for the labelling, packaging and distribution of Corbus clinical supplies. Oversight of inventory at warehouses and distribution facilities. Collaborate with CMC and Clinical Operations to develop material lot use strategies. Creation and maintenance of demand forecasts at a study, country and site level, in collaboration with clinical operations. Collaborate with Quality Assurance to ensure and maintain vendor qualification. Importation and customs management for clinical supplies. Working with partners to manage comparators and auxiliary supplies. Work with Global Regulatory Affairs, QPs, Quality Assurance and other stakeholders to ensure timely release of supplies. IRT CMC Management. Requirements: Minimum of a bachelor’s degree or equivalent experience. Min 5 years in a related supply chain role at a biotech or pharmaceutical company. Experience with managing investigational supplies for blinded and open label studies. Proficiency with IWRS/IVRS. APICS CPIM or CSCP Certification preferred. Experience managing schedules and priorities. Experience with cGMP operations is preferred. Proficiency in use of MS Excel, Project and other applications. Excellent interpersonal, verbal and written communication skills.
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