Valid8 Financial, Inc.
Clinical Supply Chain Mgmt. (Part-Time Contractor)
Valid8 Financial, Inc., San Francisco, California, United States, 94199
Clinical Supply Chain Mgmt. (Contractor)
Reports To: ED, Technical Operations
Department: CMC
About the Job
Working 15-20 hours per week, the
Clinical Supply Chain Mgmt. Contractor
will oversee end-to-end supply chain operations for monoclonal antibody investigational products used in global clinical trials. This role ensures timely, compliant, and cost-effective delivery of IP to clinical sites, while maintaining product integrity and adherence to Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) standards. Core Values
The below core values drive all that we do here at Star. We are looking for like-minded individuals that feel passionately about these same values to work with our team. Patients are our Center of Gravity: We partner with patients in unique ways, to uncover and address their unmet needs. Propelled by Data, Guided by Intuition, Informed by Expertise: We boldly explore new diseases, novel biology, and smart ways of working with a sense of urgency. Mission Ready Crew: With courage and agility, we opportunistically challenge conventional wisdom and foster an environment of respect and continuous growth. Responsibilities
Execute supply chain strategies for IP across multiple clinical programs. Forecast demand based on enrollment projections and protocol requirements. Manage inventory levels to prevent shortages or overages. Manage ancillary supplies for Clinical Trial Sites Collaborate with Clinical Operations, Regulatory, Quality, and Manufacturing teams to align supply plans with trial timelines. Ensure IP labeling, packaging, and distribution comply with regulatory and protocol requirements. Coordinate with depots and logistics providers for global distribution. Maintain documentation for chain of custody, temperature control, and product traceability. Ensure compliance with GMP, GCP, ICH guidelines, and local regulatory requirements. Support audits and inspections related to IP supply chain. Identify and mitigate supply chain risks, including cold-chain failures and regulatory delays. Develop contingency plans for critical supply disruptions. Education, Experience & Qualifications
Bachelor’s degree in Supply Chain Management, Project Management, Life Sciences, Pharmacy, or related field plus 4 years of experience or Master’s degree with 2 years of experience 4+ years of experience in clinical trial supply chain management, preferably with biologics or monoclonal antibodies. Strong knowledge of GMP, GCP, and global regulatory requirements. Experience with cold-chain logistics and temperature-sensitive products. Excellent project management and cross-functional collaboration skills. Proficiency in supply chain planning tools and ERP system About Star Therapeutics
Star Therapeutics is a Phase 3 clinical stage biotechnology company that aims to discover and develop best-in-class antibody therapies to transform the lives of patients with serious diseases. Founded by former True North executives, Star has built a team with significant scientific, clinical, regulatory, and commercial experience that has a demonstrated track record of success and is backed by top-tier biotech investors. We pride ourselves on our collective passion in bringing innovative therapies to the clinic and are committed to patients for whom no or limited treatment options exist. Star is headquartered in South San Francisco, CA. More information about Star can be found on our website at www.star-therapeutics.com . We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender identity, sexual orientation, age, marital status, veteran status, or disability status. We anticipate the pay rate for the Clinical Supply Chain Mgmt. Contractor position in our South San Francisco, CA office to range from $100 to $130 per hour and will depend on current market data and the candidate’s qualifications for the role, including education, experience and geographic location. The compensation described above is subject to change and could be higher or lower than the range described based on several factors. Please note this position is an SSF office / hybrid / remote position. NO PHONE CALLS or AGENCIES, please. Apply for this job
First name Last name Email address Location Phone number Resume Attach resume Attach another file Attach file Are you authorized to work in the United States? Are you authorized to work in the United States? Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)? Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)?
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Reports To: ED, Technical Operations
Department: CMC
About the Job
Working 15-20 hours per week, the
Clinical Supply Chain Mgmt. Contractor
will oversee end-to-end supply chain operations for monoclonal antibody investigational products used in global clinical trials. This role ensures timely, compliant, and cost-effective delivery of IP to clinical sites, while maintaining product integrity and adherence to Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) standards. Core Values
The below core values drive all that we do here at Star. We are looking for like-minded individuals that feel passionately about these same values to work with our team. Patients are our Center of Gravity: We partner with patients in unique ways, to uncover and address their unmet needs. Propelled by Data, Guided by Intuition, Informed by Expertise: We boldly explore new diseases, novel biology, and smart ways of working with a sense of urgency. Mission Ready Crew: With courage and agility, we opportunistically challenge conventional wisdom and foster an environment of respect and continuous growth. Responsibilities
Execute supply chain strategies for IP across multiple clinical programs. Forecast demand based on enrollment projections and protocol requirements. Manage inventory levels to prevent shortages or overages. Manage ancillary supplies for Clinical Trial Sites Collaborate with Clinical Operations, Regulatory, Quality, and Manufacturing teams to align supply plans with trial timelines. Ensure IP labeling, packaging, and distribution comply with regulatory and protocol requirements. Coordinate with depots and logistics providers for global distribution. Maintain documentation for chain of custody, temperature control, and product traceability. Ensure compliance with GMP, GCP, ICH guidelines, and local regulatory requirements. Support audits and inspections related to IP supply chain. Identify and mitigate supply chain risks, including cold-chain failures and regulatory delays. Develop contingency plans for critical supply disruptions. Education, Experience & Qualifications
Bachelor’s degree in Supply Chain Management, Project Management, Life Sciences, Pharmacy, or related field plus 4 years of experience or Master’s degree with 2 years of experience 4+ years of experience in clinical trial supply chain management, preferably with biologics or monoclonal antibodies. Strong knowledge of GMP, GCP, and global regulatory requirements. Experience with cold-chain logistics and temperature-sensitive products. Excellent project management and cross-functional collaboration skills. Proficiency in supply chain planning tools and ERP system About Star Therapeutics
Star Therapeutics is a Phase 3 clinical stage biotechnology company that aims to discover and develop best-in-class antibody therapies to transform the lives of patients with serious diseases. Founded by former True North executives, Star has built a team with significant scientific, clinical, regulatory, and commercial experience that has a demonstrated track record of success and is backed by top-tier biotech investors. We pride ourselves on our collective passion in bringing innovative therapies to the clinic and are committed to patients for whom no or limited treatment options exist. Star is headquartered in South San Francisco, CA. More information about Star can be found on our website at www.star-therapeutics.com . We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender identity, sexual orientation, age, marital status, veteran status, or disability status. We anticipate the pay rate for the Clinical Supply Chain Mgmt. Contractor position in our South San Francisco, CA office to range from $100 to $130 per hour and will depend on current market data and the candidate’s qualifications for the role, including education, experience and geographic location. The compensation described above is subject to change and could be higher or lower than the range described based on several factors. Please note this position is an SSF office / hybrid / remote position. NO PHONE CALLS or AGENCIES, please. Apply for this job
First name Last name Email address Location Phone number Resume Attach resume Attach another file Attach file Are you authorized to work in the United States? Are you authorized to work in the United States? Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)? Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)?
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