The posting
Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
What You'll Do
As the Senior Manager/Associate Director, Medical Affairs, reporting into the Executive Director, Skeletal Dysplasia, you will play a key role in the execution of Medical Affairs activities across the skeletal dysplasia portfolio. This role will have primary responsibility for medical review and MLR submissions, scientific content development, advisory board and company-sponsored symposium execution, Medical Information support, support for exploratory analyses of existing data and data generation opportunities, and management of external agency deliverables. You will independently drive assigned workstreams from development through approval and execution, while partnering closely with Medical Directors and functional leads on scientific and strategic decisions. This is a hands-on, individual-contributor role for someone who combines strong scientific judgment with disciplined project execution and can move complex Medical Affairs deliverables forward with limited oversight.
Responsibilities
- Serve as a Medical Affairs reviewer for scientific and medical materials, ensuring scientific accuracy, appropriate interpretation of clinical data, consistency with source documentation, and alignment with approved scientific communications, and escalate questions of clinical interpretation or strategic positioning to the responsible Medical Director.
- Initiate, submit, and independently manage Medical Affairs materials through the Medical, Legal, and Regulatory (MLR) review process, including submission preparation, reference documentation, incorporation of reviewer comments, version control, resubmission, and tracking through final approval.
- Partner with the Medical Information lead to identify needs for new or updated response materials and review Medical Information letters for scientific accuracy, appropriate data interpretation, and consistency with current evidence.
- Support development and revision of Medical Information content in collaboration with the Medical Information lead and relevant subject-matter experts.
- Manage execution of Medical Affairs advisory boards, including advisor coordination, timelines, pre-read materials, meeting logistics, agency management, MLR review, and post-meeting deliverables, in partnership with Medical Operations and other internal teams.
- Work closely with Medical Directors to support development of advisory board objectives, agendas, discussion questions, presentations, and scientific content.
- Support development and execution of company-sponsored scientific symposia, working with Medical Directors, external faculty, and KOLs to develop presentations and scientific content and to coordinate faculty review, MLR submission, revisions, and finalization of materials.
- Support Medical Directors and Clinical Development in exploring and conducting novel analyses of existing clinical trial, natural history, and real-world data (e.g., post hoc, subgroup, and descriptive analyses), including helping frame analysis questions, coordinating with Biostatistics and Data Management, and summarizing results for internal review and scientific communications.
- Assist in identifying and evaluating data generation opportunities (e.g., investigator-initiated studies, registries, chart reviews, and real-world evidence collaborations) by supporting data gap assessments, preparing concept summaries, and coordinating cross-functional input, with prioritization and approval decisions remaining with Medical Affairs leadership.
- Manage day-to-day relationships with Medical Affairs agencies and external vendors supporting assigned programs. Partner with Medical Operations to ensure contracts, statements of work, purchase orders, and required approvals are in place, then independently manage vendor timelines, deliverables, meetings, revisions, and execution.
- Track project milestones, risks, dependencies, and budgets in partnership with Medical Operations and functional leads, and proactively identify and resolve executional issues.
- Partner across Medical Affairs, Scientific Communications, Field Medical/MSL, Medical Information, Clinical Development, Regulatory, Legal, Medical Operations, and other functions to execute priority Medical Affairs initiatives.
Where You’ll Work
This is either a hybrid role requiring in-office collaboration 2-3x per week in our San Francisco Office, or a U.S.-based remote role that will require quarterly, or as needed, visits to our San Francisco Office.
Travel up to 50% is expected for scientific congresses, advisory boards, company-sponsored symposia, KOL engagements, and key internal meetings.
Who You Are
- PharmD, PhD, genetic counseling degree, NP/advanced practice degree, MS, or another relevant advanced scientific or healthcare degree. Candidates with an MS or similar degree should have 5 or more years of demonstrated pharmaceutical or biotechnology Medical Affairs experience.
- Typically 3–5 years of pharmaceutical or biotechnology Medical Affairs experience, including hands-on experience with medical review and MLR submissions, scientific content development, and advisory board or symposium execution. Candidates with a PharmD or PhD may qualify with less industry experience if supported by a Medical Affairs fellowship or equivalent.
- Strong project-management and organizational skills, with the ability to independently manage multiple complex workstreams and deadlines.
- Strong scientific writing and communication skills with exceptional attention to detail.
- Working knowledge of clinical trial data and basic biostatistical concepts, with the ability to help frame analysis questions, interpret outputs, and summarize findings accurately.
- Able to distinguish between executional decisions that can be independently managed and scientific or strategic issues that require escalation
- Experience in pediatric rare disease, genetics, skeletal dysplasia, or launch-stage Medical Affairs is preferred but not required.
- Able to travel as needed and legally authorized to work in the United States.
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.
Salary
$165,000—$210,000 USD
As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
For BridgeBio Full-Time U.S Based Roles:
Financial & Rewards
- Market-leading compensation
- 401(k) with employer match
- Employee Stock Purchase Program (ESPP)
- Pre-tax commuter benefits (transit and parking)
- Referral bonus for hired candidates
- Subsidized lunch and parking on in-office days
Health & Well-Being
- 100% employer-paid medical, dental, and vision premiums for you and your dependents
- Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
- Fertility & family-forming benefits
- Expanded mental health support (therapy and coaching resources)
- Hybrid work model with flexibility
- Flexible, “take-what-you-need” paid time off and company-paid holidays
- Comprehensive paid medical and parental leave to care for yourself and your family
Skill Development & Career Paths:
- People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
- We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
- We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
By applying, you acknowledge that BridgeBio will process your personal information as described in our Global Candidate Privacy Notice. Questions or requests: [email protected]
