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Manager, Clinical Supply Chain Management

Company

BridgeBio
Address , San Francisco, Ca
Employment type FULL_TIME
Salary $127,000 - $155,000 a year
Expires 2023-07-21
Posted at 11 months ago
Job Description
About Eidos Therapeutics & BridgeBio Pharma

Eidos Therapeutics, an affiliate of BridgeBio Pharma, is a clinical-stage biopharmaceutical company focused on addressing the large and growing unmet need in diseases caused by transthyretin, or TTR, amyloidosis, or ATTR. We seek to treat this well-defined family of diseases at their collective source by stabilizing TTR. Our investigational product, acoramidis (AG10), is an orally administered small molecule designed to potently stabilize TTR, a potentially best-in-class treatment aiming to halt the progression of ATTR diseases.

BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.

Our focus on scientific excellence and rapid execution aims to translate today’s discoveries into tomorrow’s medicines. We have U.S. offices in San Francisco, Palo Alto, Boston, New York, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zug, Switzerland, and are expanding across Europe.

To learn more about our story and company culture, visit us at eidostx.com/ | https://bridgebio.com

Who You Are

The Clinical Supply Chain Management Manager is responsible for coordinating investigational medicinal product (IMP) planning, forecasting, labeling, packaging, distribution, inventory monitoring, and reconciliation for assigned clinical studies. This position reports to the Exe. Director, Clinical Supply Management.

Responsibilities

  • Support projects and process improvement efforts related to supply chain management
  • Develop and manage SOPs, work instructions, processes, systems, and forms governing supply chain management in alignment with industry standards and regulatory requirements
  • Individuals Who Inspire Excellence in themselves and those around them
  • Develop plans for ancillary supply sourcing and liaise with the CMC team to ensure ancillary compatibility with IMP, as required.
  • Collaborate cross-functionally with Clinical Operations, Manufacturing, Regulatory Affairs, and Quality Assurance to plan and execute IMP supply planning, including labeling and packaging, inventory control, and depot management for assigned clinical studies
  • High-quality executors, who execute against goals and milestones with quality, precision, and speed
  • Develop, update, and adapt clinical supplies distribution plans based on program and study timelines, trial design, clinical program changes, recruitment, geography, and manufacturing schedules
  • Coordinate with Manufacturing Operations, Quality Assurance, and Regulatory Affairs to ensure planned IMP release testing/re-testing, stability, expiry dates, labeling, and packaging schedules align with program milestones, adjusting as necessary throughout the program
  • Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset
  • Patient Champions, who put patients first and uphold strict ethical standards
  • Coordinate and manage clinical supplies forecasting and utilization to ensure on-time and reliable availability of IMP and required ancillary supplies in support of study execution
  • Truth Seekers, who are detailed, rational, and humble problem solvers
  • Serve as liaison between Clinical Operations and Quality Assurance to manage IMP shelf-life extensions, temperature deviation management, product complaints, and associated investigations
  • Obtain and review quotes and approve purchase requisitions and invoices.

Education, Experience & Skills Requirements

  • Ability to proactively perform and complete duties with minimal supervision in an accurate and timely manner
  • Proficient in MS Office (Word, Excel, and PowerPoint)
  • Solid vendor management skills
  • Experience with ERP Planning Systems, Project management, and/or commercial launch readiness experience is a plus
  • Effective interpersonal, written, and verbal communication skills
  • Able to critically evaluate and prioritize job tasks and the impact on overall study execution
  • Exceptional organizational skills with the ability to multi-task and prioritize
  • Strong computer, database, and organizational skills required
  • Effectively collaborates with cross-functional team members
  • Thorough understanding of cGMP, GCP, and ICH standards governing IMP labeling, packaging, and global distribution (GDP)
  • Experience with electronic interactive response technologies for inventory management
  • Strong problem-solving capabilities
  • Ability to work in a team or independently
  • Attention to detail
  • Minimum of 4 years in clinical supply chain management function
  • Ability to work with distributed team members and outside vendors
  • 4-year college degree (relevant discipline preferred)

What We Offer

  • Commitment to Diversity, Equity & Inclusion – with initiatives like Women at Bridge, we are committed to fostering an inclusive environment where every person feels seen, valued, and heard
  • Rapid career advancement for strong performers
  • An unyielding commitment to always putting patients first. Learn more about how we do this here
  • A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science
  • A place where you own the vision – both for your program and your own career path
  • Flexible PTO
  • Access to learning and development resources to help you get in the best professional shape of your life
  • A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak
  • Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs)
  • Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time
  • Partnerships with leading institutions
  • A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game
  • Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts
$127,000 - $155,000 a year
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. The anticipated salary range for candidates for this role who will work in California is $127,000 to $155,000/year. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
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