About Eidos Therapeutics & BridgeBio Pharma
Eidos Therapeutics, an affiliate of BridgeBio Pharma, is a Phase 3 developmental-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, 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.
Who You Are
The Executive Director/Sr. Director, Medical Information Content & Strategy, Medical Affairs (Acoramidis), is responsible for developing and executing comprehensive medical information and communication strategies to support healthcare professionals, patients, and internal stakeholders. This position will play a crucial role in providing accurate, timely, and relevant medical information while ensuring compliance with regulatory guidelines and maintaining the highest standards of ethical conduct. Leading the development of medical content and execution of medical affairs strategy for Acoramidis. This includes the development and implementation of the scientific platform and lexicon, the development of the dossier and FAQs, designing the digital medical platform, leading the Legal/Medical/Regulatory Review Process, preparing standard response letters, and management of the Call Center for the organization. The candidate will have a solid clinical and scientific background, a deep understanding of the pharmaceutical industry, and a proven track record of success in leading and managing teams within matrixed environments – such as with clinical development, regulatory, market access, commercial -- to generate momentum to further the business in support of patients.
Responsibilities
- Collaboratively develop and implement the overall medical information strategy to support Acoramidis
- Oversee the creation and dissemination of medical content, including medical standard response letters, FAQs, scientific publications; ensure the accuracy, relevance, and consistency of content across all communication channels
- Ensure compliance with applicable regulations, industry standards, and company policies related to medical information and communication, as well as accurate and compliant medical content for promotional materials and other customer-facing materials
- Act as a primary point of contact for medical information inquiries from external stakeholders (HCPs, patients, caregivers, etc.), ensuring timely and accurate responses
- Develop and implement the scientific platform and lexicon to be utilized across the organization
- Establish relevant SOPs to ensure process alignment across the department
- Partner with corporate IT to design and execute on a digital/web-based platform strategy to support medical information and communications
- Prepare the Dossier for Acoramidis for distribution to external customers
- Represent the company at scientific conferences, and other events when needed
- Stay up-to-date on the latest approaches to medical information through medical research, competitive information, and attendance at professional society meetings for medical information
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
- Advanced degree (MD or PhD or equivalent) in life sciences or related field preferred
- At least 12 years of professional experience with greater than 5 years in the pharmaceutical/biotechnology industry, with experience in medical information, medical communications, or medical affairs (cardiovascular focus preferred)
- Proven track record of developing and executing successful medical information and communication strategies
- Previous experience managing functional budgets including vendor relationships
- Understanding of medical content development, global regulatory requirements, and industry guidelines
- Excellent leadership skills and exceptional communication and interpersonal skills to interact effectively with internal and external stakeholders
- Solid clinical and scientific acumen
- Ability to work independently and as part of a team in fast-paced environments
- Ability to manage multiple priorities and meet deadlines
- Commitment to excellence, continuous learning, flexibility, and persistence
- Demonstrated ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously
- And, most importantly, a genuine passion for improving patient lives through scientific innovation
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
- Partnerships with leading institutions
- Commitment to Diversity, Equity & Inclusion
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