Responsibilities:

• Strategic Leadership: Develop and execute an innovative and family access strategy aligned with BridgeBio's objectives, aiming to ensure that people living with rare conditions can access the company's products

• Team Leadership: Manage a team of Family Access Managers (FAM); Provide leadership, coaching, and support to ensure the team's maximum effectiveness

• Family Access Strategy: Oversee the development of FAM tools and execution of access strategies, which may involve working with pharmacies, health systems, and providers to secure patient access for family

• Cross-Functional Collaboration: Evaluate and align with BridgeBio advocacy team on advocacy meetings to attend and represent BridgeBio

• Compliance: Ensure that all reimbursement and patient access activities adhere to healthcare regulations and corporate compliance requirements, including relevant laws and industry standards

• Stakeholder Collaboration: Collaborate with healthcare providers (prescribers and well as staff), payers, the Hub and pharmacies to facilitate patient access and address access challenges

• Data Analysis: Utilize data analysis and reporting tools to evaluate the efficiency and effectiveness of family access processes, finding areas for improvement and implementing necessary changes

• Policy and Market Analysis: Stay updated on changes in healthcare policy, market dynamics, and healthcare trends that may impact patient access

• Budget Management: Manage the budget for team of FAMs, ensuring cost-effective resource allocation

• Quality Assurance: Implement quality assurance measures to ensure each member adheres to the team’s standards and expectations

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:

• Bachelor's or advanced degree in a relevant field (Healthcare Administration, Business, Nursing, Genetics, Pharmacy, etc.). Master's degree or equivalent is a plus

• 15+ years of Access and/or sales experience in the Pharmaceutical or Healthcare industries, including rare disease experience and launch experience

• 5+ years of leading and developing high performing teams

• Experience in Patient Services, Market Access, Reimbursement or Patient Access Management preferred

• Experience working with Specialty Pharmacy Networks and Patient Services Hubs

• In-depth knowledge of healthcare reimbursement processes and healthcare regulations

• Exceptional leadership and team management skills

• Strong knowledge of the payer environment, including government (Medicaid) and commercial payers

• Effective communication and interpersonal skills for collaboration with stakeholders

• Proficiency in data analysis, reporting tools, and AI

• Genetics, Endocrinology, Rare Disease experience is a plus

• Strong knowledge and understanding of Compliance with HIPAA regulations, OIG guidance, Advertising and Promotion requirements, the Anti-Kickback Statute, and applicable policies, best practices, and guidelines

• Commitment to patient-centered support and ensuring access to innovative treatments

• Up to 50-60% Travel; including occasional weekends

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 USA 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

What You'll Do

BridgeBio is seeking a highly strategic and execution-oriented HEOR leader to define and drive the global evidence strategy for acoramidis in ATTR-CM. This individual will play a pivotal role in enabling successful global launch, optimizing payer access, and sustaining long-term product differentiation in an increasingly competitive and evolving landscape.

As the global HEOR lead, this role will shape the evidence generation agenda across the product lifecycle—spanning clinical development, launch, and post-marketing—leveraging real-world evidence (RWE), comparative effectiveness research, and patient-centered outcomes. The leader will serve as a key partner to Market Access, Medical Affairs, Clinical Development, and Commercial teams to ensure evidence translates into impactful value narratives for payers and HTA bodies worldwide.

Why This Role Matters

Acoramidis represents a transformative opportunity in ATTR-CM. This role is central to articulating and proving its value to patients, providers, and payers globally. By shaping the evidence strategy and driving impactful insights, this leader will directly influence access, adoption, and long-term success in a competitive and rapidly evolving therapeutic area.

Key Responsibilities

• Global HEOR Strategy: Define and lead the end-to-end global HEOR strategy for acoramidis across launch and lifecycle, ensuring alignment with clinical, regulatory, and commercial objectives and driving evidence-based decision-making

• Evidence Generation & Data Strategy: Design and oversee innovative real-world evidence (RWE), economic models, and data partnerships (e.g., claims, EHR, observational survey datasets) to support value demonstration and long-term evidence generation

• Payer & HTA Readiness: Develop robust, payer-relevant evidence packages and lead HEOR contributions to global HTA submissions, pricing, reimbursement, and access strategies

• Publications & Scientific Dissemination: Lead the HEOR publication strategy, including congress planning and peer-reviewed publications with Pubs teams, to establish a compelling and credible evidence narrative

• Patient-Centered Outcomes: Drive the development and integration of PROs and other patient-centered endpoints to demonstrate meaningful clinical benefit and differentiation

• Competitive Intelligence & Positioning: Proactively assess and anticipate competitive dynamics (including generics, pipeline entrants, and alternative therapies) to inform evidence strategy and positioning

• Cross-Functional Leadership: Partner closely with Market Access, Medical Affairs, Clinical, Regulatory, and Commercial teams to ensure cohesive and actionable evidence strategies

• Governance & Scientific Integrity: Ensure HEOR activities are conducted with scientific rigor and appropriate governance, maintaining independence of evidence generation while enabling compliant, impactful use

• External Engagement: Oversee external vendors, research partners, and academic collaborations to deliver high-quality, timely evidence outputs

Where You'll Work

This is a onsite role and requires in-office collaboration 2-3x per week in our San Francisco and Palo Alto Offices.

Who You Are

• Advanced degree (PhD, PharmD, MPH, MD, or equivalent) in health economics, outcomes research, epidemiology, or related field

• 10+ years of progressive HEOR experience within biopharma or consulting, including leadership of global programs

• Demonstrated experience supporting product launches and payer strategy development in specialty or rare diseases preferred

• Strong understanding of global HTA frameworks (e.g., NICE, ICER, CADTH, G-BA) and payer evidence requirements

• Proven track record in RWE, economic modeling, and PRO strategy development

Key Competencies

• Strategic, enterprise-level thinker with strong business acumen

• Ability to translate complex evidence into clear, compelling value narratives for diverse stakeholders

• Influential cross-functional leader with a collaborative and proactive mindset

• Strong project leadership and ability to manage multiple priorities in a fast-paced environment

• Executive presence with excellent communication and stakeholder engagement skills

#LI-LN1

What You'll Do

BridgeBio is seeking an Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

About BridgeBio Pharma, Inc. 

BridgeBio is a biopharmaceutical company dedicated to discovering, developing, and delivering transformative medicines for patients living with genetic diseases and genetically defined cancers. Since our founding in 2015, we have built a diverse portfolio of more than 20 drug development programs, ranging from early discovery to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide. 

Who We Are 

BridgeBio is a global biotechnology company with our Global Headquarters located in San Francisco, USA, and our International HQ located in Zug, Switzerland. Since establishing our European presence in 2021, we’ve been building empowered, high-performing teams across countries — with experienced colleagues who move quickly, take ownership, and are fueling the company’s international growth. 

At BridgeBio, you’ll find an energetic and collaborative culture where pragmatism meets bold decision-making. We embrace uncertainty with confidence, guided by our commitment to making a meaningful impact for patients. Our people are trusted and empowered, united by urgency, purpose, and the drive to advance science for patients around the world. 

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

What You'll Do

You will report to the General Manager, Europe Central Region and work closely with international Market Access, and local, regional and global Medical Affairs, as well as with our local field-based colleagues, to drive strategic initiatives that support BridgeBio’s mission of delivering transformative medicines to patients with genetic diseases and genetically driven cancers. 

Your primary purpose will be to secure timely, sustainable patient access to the company’s first products by shaping the value narrative, and leading pricing and reimbursement strategy and execution of related dossier, negotiation and cost coverage application work. In this role you ensure we meet our Market Access ambitions aligned with clinical value and global pricing interdependencies. 

You will also be a core member of the extended International Market Access team, bringing the voice of the country to the international discussion and decision-making process. 

This role requires effective collaboration with cross-functional colleagues and external stakeholders to ensure high-quality execution and impact. The ideal candidate combines deep expertise in Market Access related processes for Germany, Austria and Switzerland in the context of introducing a biotech for the first time. You are eager to make a remarkable contribution to a disease space in pre-launch and launch phase in a rare disease and orphan condition with strong communication skills, adaptability, and the ability to thrive in a fast-paced, hands-on environment. 

Responsibilities

• Develop and execute the Central Europe Region market access priorities, including pricing, reimbursement, and launch sequence, aligned with global and regional frameworks
• Lead HTA and payer engagement strategy – with a strong focus on AMNOG, ensuring early, proactive dialogue with national and regional decision-makers to anticipate requirements and reduce access risk
• Own country value dossier strategy and adaptation: incl. comparator selection, evidence gaps, risk mitigation. Thereby ensuring high-quality, locally relevant submissions delivered on time and supporting favourable reimbursement outcomes 
• Define and implement pricing strategy, including list price, net price corridors, and contracting principles, while protecting long-term value and portfolio optionality
• Coordinate cross-functionally with Medical Affairs, Commercial, Regulatory, and Finance to align evidence generation, access strategy, and launch readiness, as well as post-launch accounting of rebates and related accruals
• Develop, implement and maintain compliant incentive structures for buying groups in Germany
• Assess potential and advocate for cost coverage and tailored solutions for individual SHIs in Germany

The above job description documents the general nature and level of work but is not intended to be an exhaustive list of activities, duties, and responsibilities required of job incumbents. Therefore, job incumbents are expected to perform all other duties as assigned or required, as training and experience allow. 

Where You'll Work

This is a Germany-based role. We anticipate travel within Germany (focus) for KOL meetings and HTA process attendance, Austria, Switzerland (for internal alignment and engagement at our international office in Zug). Regular local team meetings and designated office location in Germany is Munich. 

Who You Are

• At least 5 years leading HTA submissions & pricing negotiations in the DACH region, in the context of rare diseases and orphan conditions
• Profound knowledge of the German, Austrian and Swiss healthcare systems & regulations
• Experience in generating relevant data for HTA submission & pricing negotiations, with a relevant network of agencies for related work and support
• Comfortable with presenting convincingly at senior levels & to external thought leaders
• Proven experience in project management of multidisciplinary teams (including external providers)
• Demonstrated ability to organise and execute plans against objectives in a semi-autonomous environment while working effectively in a cross-functional team environment
• Knowledge of product commercialisation processes. Hands-on and solution oriented when it comes to setting up necessary process and documentation

Rewarding Those Who Make the Mission Possible

We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.  

• Market leading compensation 
• Hybrid work model - we value your flexibility in how you work, but encourage time in the office to strengthen our culture, collaboration, and sense of community
• We provide career development through regular feedback, continuous education and professional development programs
• We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
  
  

What You'll Do

BridgeBio is seeking an Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

What You'll Do#LI-TC1

BridgeBio is looking for a Sr. Manager/Associate Director, Market Access Marketing to support the tactical execution of the Market Access strategies for BBP-418.  This encompasses all aspects of Market Access Marketing:  payer accounts, trade and distribution, pricing and contracting, patient support, and field reimbursement.

The Sr. Manager/Associate Director, Market Access Marketing will manage the end-to-end market access marketing materials, manage marketing agency vendors, and execute on all new product launch activities. The ideal candidate should be prepared to work in a fast-paced environment and must be able to collaborate with multiple stakeholders, including but not limited to Market Access, Marketing, Medical, Analytics, Legal, Regulatory, Compliance, Sales, and Training. 

Responsibilities

• Serve as the market access marketing lead responsible for all Market Access marketing tactics, including but not limited to: payer value proposition, payer communications, patient services, field reimbursement support, trade and distribution, and pricing and reimbursement support
• Oversee and manage day-to-day activities with market access marketing agencies; manage and monitor market access marketing materials budget and vendor contracts
• Develop and review key market access marketing materials and lead projects through the medical, legal, and regulatory (MLR) or promotional review committee (PRC) review and approval process
• Support launch readiness through leading Market Access planning meetings and participating in brand planning and other internal meetings
• Collaborate with training to ensure effective, impactful, best in class training for Market Access field teams
• Act as a subject matter expert on market access trends and implications for strategic planning; research competitive market access pieces and payer initiatives and keep the organization well informed of external initiatives and impact

Where You'll Work

This is a onsite role and requires in-office collaboration 2-3x per week in our San Francisco Office.

Who You Are

• BA/BS degree required; MBA preferred
• Minimum of 8+ years of Biotech/Pharma experience
• Track record of successful launch execution in Market Access, preferably in rare diseases or specialty therapeutics
• Excellent communication, leadership, analytical and strategic-thinking skills
• Ability to work under pressure and to manage and execute multiple projects simultaneously
• Strong project management skills and attention to detail
• 15 - 25% Travel
• You have demonstrated curiosity and adaptability in adopting AI-powered tools and technologies

What You'll Do

BridgeBio is seeking an Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

What You'll Do

BridgeBio is seeking a Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

What You'll Do

BridgeBio is seeking an Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

What You'll Do#LI-TC1

BridgeBio is looking for a Sr. Manager/Associate Director, Market Access Marketing to support the tactical execution of the Market Access strategies for encaleret. This encompasses all aspects of Market Access Marketing:  payer accounts, trade and distribution, pricing and contracting, patient support, and field reimbursement.

The Sr. Manager/Associate Director, Market Access Marketing will manage the end-to-end market access marketing materials, manage marketing agency vendors, and execute on all new product launch activities. The ideal candidate should be prepared to work in a fast-paced environment and must be able to collaborate with multiple stakeholders, including but not limited to Market Access, Marketing, Medical, Analytics, Legal, Regulatory, Compliance, Sales, and Training. 

Responsibilities

• Serve as the market access marketing lead responsible for all Market Access marketing tactics, including but not limited to: payer value proposition, payer communications, patient services, field reimbursement support, trade and distribution, and pricing and reimbursement support
• Oversee and manage day-to-day activities with market access marketing agencies; manage and monitor market access marketing materials budget and vendor contracts
• Develop and review key market access marketing materials and lead projects through the medical, legal, and regulatory (MLR) or promotional review committee (PRC) review and approval process
• Support launch readiness through leading Market Access planning meetings and participating in brand planning and other internal meetings
• Collaborate with training to ensure effective, impactful, best in class training for Market Access field teams
• Act as a subject matter expert on market access trends and implications for strategic planning; research competitive market access pieces and payer initiatives and keep the organization well informed of external initiatives and impact

Where You'll Work

This is a onsite role and requires in-office collaboration 2-3x per week in our San Francisco Office.

Who You Are

• BA/BS degree required; MBA preferred
• Minimum of 8+ years of Biotech/Pharma experience
• Track record of successful launch execution in Market Access, preferably in rare diseases or specialty therapeutics
• Excellent communication, leadership, analytical and strategic-thinking skills
• Ability to work under pressure and to manage and execute multiple projects simultaneously
• Strong project management skills and attention to detail
• 15 - 25% Travel
• You have demonstrated curiosity and adaptability in adopting AI-powered tools and technologies

#LI-TC1

About BridgeBio Pharma, Inc. 

BridgeBio is a biopharmaceutical company dedicated to discovering, developing, and delivering transformative medicines for patients living with genetic diseases and genetically defined cancers. Since our founding in 2015, we have built a diverse portfolio of more than 20 drug development programs, ranging from early discovery to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide. 

Who We Are 

BridgeBio is a global biotechnology company with our Global Headquarters located in San Francisco, USA, and our International HQ located in Zug, Switzerland. Since establishing our European presence in 2021, we’ve been building empowered, high-performing teams across countries — with experienced colleagues who move quickly, take ownership, and are fuelling the company’s international growth. 

At BridgeBio, you’ll find an energetic and collaborative culture where pragmatism meets bold decision-making. We embrace uncertainty with confidence, guided by our commitment to making a meaningful impact for patients. Our people are trusted and empowered, united by urgency, purpose, and the drive to advance science for patients around the world. 

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

What You'll Do

This critical role reporting to the regional General Manager - WEU, requires you to be a driven individual with a track record in navigating in the medico-economic environment, securing reimbursement, pricing & patient access to medicines in France (as a priority), Belgium, and the Netherlands.  Establish effective collaboration and communication with external stakeholders, such as healthcare professionals, payers, policy makers including representing BridgeBio and leading and/ or actively participating in HTA and pricing meetings, and the medico-economic community events is also critical. Your primary role will be to design, anticipate and drive all steps of the HTA, pricing and reimbursement process within each country and to engage with early scientific advice and early access programs where & when needed.  You will, therefore, be able to operate in a fast-paced, sometimes ambiguous environment where you will influence without authority and effectively communicate WEU market access strategies to all levels. 

Responsibilities

The responsibilities below give the general nature and level of work but are not intended to be an exhaustive list of activities, duties, and responsibilities required. Therefore, you will be expected to perform all other duties as assigned or required. 

HTA, Pricing & Reimbursement 

• Lead internal and external stakeholders to develop and execute a strategy to demonstrate the value of BridgeBio’s medicines to French, Belgian & Dutch HTA bodies/payers to ensure pricing, reimbursement and optimal patient access
• Responsible for all steps during the value assessments & pricing negotiations, i.e. evidence generation, KOL/expert support, advocacy, assessment analysis, written statements, oral hearing, pricing negotiation, and arbitration
• Ensure timely reimbursement, including developing necessary processes, forms and administrative steps for actual availability and access of BridgeBio drugs in the market
• Create and develop a strong trust relationship with key external stakeholders and decision makers, to be perceived as a partner and an advocate for patients’ access
• Develop and implement early access solutions for France (mainly) and Belgium / Netherlands

Clinical development 

• Influence clinical development plans to incorporate important endpoints and design features into clinical trials that satisfy French / WEU HTA and payers needs 

Evidence generation 

• Assess WEU region needs related to specific diseases and pipeline assets and develop and execute research programs to prepare the necessary data packages for use in HTA assessments and pricing negotiations. 
• Evaluate and propose RWE and data to support access, funding, adoption and commercial success of the drugs

Other 

• Interact effectively with patients’ groups, healthcare professionals, policy makers and payers to understand the burden of diseases that are the target of BridgeBio products
• Lead the shaping and execution of health technology assessment (HTA) early scientific advice engagement
• Assess the viability of early access programs in the region and work with internal/external stakeholders to implement them
• Effectively execute against market access plan within budget
• Manage external suppliers to develop, adapt and validate HTA deliverables (e.g., systematic literature reviews, indirect & mixed treatment comparisons, health economic models, and submission documents)
• Support the WEU teams with developing and implementing innovative value materials and tools for use by their field teams to demonstrate the products' value proposition and encourage reimbursed medicines' uptake
• Develop and maintain a network of key national & regional access, HEOR & academic leaders

The above job description documents the general nature and level of work but is not intended to be an exhaustive list of activities, duties, and responsibilities required of job incumbents. Therefore, job incumbents are expected to perform all other duties as assigned or required, as training and experience allow. 

Where You'll Work

This is a France-based role with a significant stakeholders’ facing component. We anticipate travel within France as a priority country for meetings with policy makers, payers, and conferences attendance, Belgium, the Netherlands (and Switzerland for internal alignment and engagement at our international office in Zug) and European travel for conferences and events (internal and external). Local team meetings and designated office location in France is Paris. 

Who You Are

• At least 5 - 7 years leading HTA submissions, HEOR projects, pricing negotiations and policy makers advocacy in France 
• Knowledge and experience in Belgium and the Netherlands will be a strong plus 
• Profound knowledge of the French (and Benelux) healthcare systems & regulations 
• Experience in successfully influencing clinical trial design
• Experience in generating relevant data for HTA submission, HEOR & pricing negotiations
• Experience in presenting at senior levels & to external thought leaders
• Proven experience in project management of multidisciplinary teams (including external providers)
• Experience in launching orphan / ultra-orphan drugs
• Fluent in verbal and written French and English
• Demonstrated ability to organize and execute plans against objectives in a semi-autonomous environment while working effectively in a cross-functional team environment
• Knowledge of product commercialization processes
• Highly accountable and self-disciplined leader with a sense of responsibility and ownership of projects and products 

Rewarding Those Who Make the Mission Possible

We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.  

• Market leading compensation 
• Hybrid work model - we value your flexibility in how you work, but encourage time in the office to strengthen our culture, collaboration, and sense of community
• We provide career development through regular feedback, continuous education and professional development programs
• We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
  
  

What You'll Do

BridgeBio is seeking a Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas

What You'll Do

BridgeBio is seeking an Field Reimbursement Manager – Rare Disease (Hybrid Reimbursement & Patient Support) responsible for executing the launch strategy across a rare disease portfolio including integrating provider-facing reimbursement strategy with patient access and support coordination across a rare disease portfolio.

This hybrid role operates at an Associate Director level of autonomy and cross-functional influence, serving as a regional expert in navigating complex reimbursement pathways while supporting compliant education and coordination related to patient access and support programs.

The Associate Director partners with healthcare providers, consented patients and care partners, specialty pharmacies, and internal stakeholders to support patient understanding of reimbursement, affordability, and access processes in a compliant and ethical manner.

This position reports into Market Access / Patient Services leadership and works in close collaboration with Medical, Compliance, Legal, Commercial, Sales, and Patient Services teams.

Responsibilities

Reimbursement & Access Strategy (Provider-Facing)

• Serve as a regional subject matter expert on reimbursement and access for BridgeBio therapies
• Educate healthcare provider offices on reimbursement processes, including benefits investigation, prior authorization, appeals, and coverage pathways
• Identify and compliantly address access barriers within commercial and government payer environments
• Support integration of access processes into provider office workflows
• Provide compliant education on BridgeBio patient support programs and services
• Share payer policy trends and field insights with Market Access leadership to inform strategy

Patient Support & Access Coordination

• Provide access and affordability education to consented patients and care partners in alignment with compliance and privacy regulations
• Support understanding of reimbursement processes and available patient support resources
• Coordinate, as appropriate, among hubs, specialty pharmacies, prescriber offices, and support programs to facilitate continuity of access
• Assist in identifying and escalating access-related challenges impacting the patient journey
• Support onboarding and ongoing engagement of consented patients within BridgeBio patient support programs in accordance with program rules

Cross-Functional Leadership & Insight Generation

• Act as a senior field partner to Market Access, Patient Services, Compliance, Legal, Medical, Commercial, and Sales teams
• Provide compliant, de-identified field insights regarding access trends, barriers, and process gaps
• Contribute to the development and refinement of access strategies, tools, and field materials
• Participate in cross-functional initiatives aimed at improving patient access pathways
• Serve as a mentor and resource to field access colleagues where appropriate

Compliance & Ethical Standards

• Operate in strict adherence to all company policies and applicable laws and regulations, including HIPAA and OIG guidance
• Provide patient-facing support in a hybrid setting while operating in strict adherence to company policies and all applicable laws and regulations, including HIPAA and OIG requirements
• Ensure all interactions with patients, providers, and stakeholders are compliant, non-promotional, and within scope
• Properly handle protected health information (PHI) in accordance with company policy

Scope & Impact

• Senior individual contributor with successful lateral leadership experience and enterprise impact
• Operates with a high degree of autonomy and professional judgment
• Manages complex and escalated access and reimbursement challenges
• Influences access strategy through field-based insights and cross-functional collaboration

Where You'll Work

This is a U.S.-based field role requiring greater than 50% domestic travel based on regional needs.

Who You Are

Required:

• Bachelor’s degree required
• 8+ years of experience in biotech/pharma, with significant experience in reimbursement, market access, patient services, or rare disease
• Deep understanding of U.S. payer systems, including commercial and government coverage pathways
• Experience navigating specialty pharmacy and hub models
• Strong knowledge of compliance requirements related to patient support and access services
• Ability to work independently in a field-based, cross-functional environment

Preferred:

• MBA, RN, or other advanced clinical or business degree preferred
• Rare disease experience
• Experience supporting both provider reimbursement and patient access programs
• Experience working with complex health systems and specialty centers
• Background in cardiology, neurology, pediatrics, or other specialty therapeutic areas