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Palo Alto

    Associate Director/Director, Clinical Quality Assurance Remote - Palo Alto, United States - BridgeBio

    BridgeBio
    BridgeBio Palo Alto, United States

    3 days ago

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    Description
    About BridgeBio Gene Therapy & BridgeBio Pharma
    BridgeBio Gene Therapy, a subsidiary of BridgeBio Pharma , is focused on discovering and developing drugs for patients with grievous genetic diseases


    We do this by:
    Finding the right starting points to target diseases at their source.

    Using a combination of a systematic assessment of the genetic disease landscape and informed diligence on the latest research, we find indications with clear mechanisms of pathogenesis that are ripe for translation into disease-modifying drugs.

    Building products with world-class R&D personnel.

    We employ industry-leading scientists that work closely with leading academics to prosecute a wide variety of drug programs at the highest level of scientific rigor.

    Our team combines biopharmaceutical veterans with up-and-coming leaders to drive entrepreneurial thinking grounded by experience.
    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, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zurich, Switzerland, and are expanding across Europe.

    Reporting to the Executive Director, Clinical Quality Assurance, the Associate Director/Director, Clinical Quality Assurance will define and support the quality oversight and management of GCP activities internally at BBGT (and other affiliates as directed) and externally with BBGT vendors, consultants, and service providers, including, but not limited to, quality systems management, document review, and approval.

    The ideal candidate will have experience working in a GCP practice area, preferably in the biotech/pharmaceutical sector.
    Responsibilities

    Direct the management and maintenance of Clinical aspects of BBGT's Quality Management System procedures and related processes for continuous improvement
    Partner with clinical study teams to coordinate appropriate and timely documentation of quality event management, including corrective action and preventive action (CAPA) plans, as necessary
    Provide Clinical Quality Assurance (GCP) leadership and Subject Matter Expertise (SME) to clinical study teams
    Author and maintain QA Standard Operating Procedures (SOPs). Support management of other functional area SOPs
    In collaboration with functional area leads, support training oversight
    Lead process improvement projects as needed
    Provide Clinical Quality Assurance SME to reviews of clinical protocols, amendments, Clinical Study Reports, and other clinical trial-related documents
    Plan, conduct, and/or assist in internal and external service provider audits. Review audit reports, and any corresponding corrective and preventative actions for adequacy
    Lead inspection readiness activities and provide support for audits and inspections conducted by external sources (e.g., health authorities) as applicable
    Other duties as assigned or required
    No matter your role at BridgeBio, successful team members are:
    Patient Champions, who put patients first and uphold strict ethical standards
    Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset
    Truth Seekers, who are detailed, rational, and humble problem solvers
    Individuals Who Inspire Excellence in themselves and those around them
    High-quality executors, who execute against goals and milestones with quality, precision, and speed
    Education, Experience & Skills Requirements

    Ability to build relationships and work collaboratively with a variety of individuals within the department, company, and vendors
    Strong negotiation skills, flexibility, and ability to provide a solution-based approach to emerging challenges
    Ability to simultaneously handle multiple project issues while dealing with time demands, incomplete information, or unexpected events
    Bachelor's degree in a scientific discipline or equivalent experience
    Minimum of 8 years of experience in a GCP practice area; Clinical Quality Assurance or similar role preferred
    Expertise with applicable GCP guidelines
    What We Offer

    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
    A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak
    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
    A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game
    Access to learning and development resources to help you get in the best professional shape of your life
    Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs)
    Flexible PTO
    Rapid career advancement for strong performers
    Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time
    Commitment to Diversity, Equity & Inclusion

    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.

    Below is the anticipated salary range for candidates for this role who will work in California.

    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, location of residence 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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