Senior Director, Clinical Science
BridgeBio
Summary
Join Eidos Therapeutics, a BridgeBio Pharma affiliate, as an Executive Director/Sr. Director, Clinical Science, Medical Affairs. You will be responsible for advancing clinical science in ATTR-CM and related fields, supporting patients. Key responsibilities include content creation for publications, protocol ideation, review of clinical materials, and customer engagement. The role requires an advanced medical degree, significant experience in the pharmaceutical/biotechnology industry, and proven success in Phase 4 studies. Strong leadership, communication, and clinical science acumen are essential. BridgeBio offers a competitive compensation and benefits package, including flexible PTO, opportunities for career advancement, and a collaborative work environment.
Requirements
- Advanced degree (MD, DO, MBBS) in medicine required; subspecialization in cardiovascular diseases a plus
- At least 5 years of professional experience with more than 5 years in the pharmaceutical/biotechnology industry and experience in medical affairs (cardiovascular focus highly preferred)
- Proven track record of developing and executing successful Phase 4 studies, including registries and real-world interventional studies
- Ability to apply scientific rigor to understand and debate detailed clinical science aspects of disease areas and approach clinical science discussions with confidence and curiosity, both internally and externally
- Ability to develop advanced clinical content, including protocols (cardiovascular focus strongly preferred)
- Previous experience managing functional budget including vendor relationships
- Familiarity with and understanding of 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 science acumen (cardiovascular focus strongly preferred)
- 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
Responsibilities
- Content ideation, writing or review, or both, for abstracts, manuscripts, ad boards includes ensuring deliverables happen on time through correct process steps
- Protocol ideation and syndication with KOLs, writing or review, or both, for any Med Affairs study, including HEOR; "site monitors" for all clinical studies; includes ensuring deliverables happen on time through correct process steps
- Review of any clinical material (e.g., SRLs, regulatory documents like PBRERs) that Med Affairs generates or is asked to review
- Supplement customer engagement broadly written (e.g., at congresses, in the field where appropriate, ad boards, steercos), leading certain initiatives (e.g., compendia, global access initiatives) that impact clinical care
- Develop and optimize clinical strategy (with cross-functional collaboration): translate clinical science and insights into post-launch clinically relevant short- and long-term plans (abstracts, manuscripts, studies, registries, etc.)
- Translate unmet clinical needs and clinical implications of diagnostic and treatment dynamics into Medical plans that improve clinical outcomes
Preferred Qualifications
- Subspecialization in cardiovascular diseases
- Cardiovascular focus
- Cardiovascular focus
Benefits
- 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
- 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 β 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