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Sr. Director Evidence Generation

12 hours, 13 minutes ago
United States
Full-time
Lead
Program Manager
Project and Program Management
Apply Now
bridgebiowp

bridgebiowp

bridgebiowp is a biotechnology firm focused on designing transformative medicines specifically for patients suffering from genetic diseases and cancers that have identifiable genetic drivers.

Pharmaceuticals
251-1K
Founded 2014
$2300M raised
View All Jobs 18

Description

  • Lead the development and execution of the integrated evidence generation strategy for skeletal dysplasia programs.
  • Design and oversee real-world evidence initiatives, including registries, natural history studies, external data collaborations, and database analyses.
  • Partner with HEOR to generate data supporting value demonstration, payer engagement, and health technology assessment requirements.
  • Lead Phase 4 planning and execution, including post-marketing commitments and lifecycle management studies.
  • Develop and manage investigator-initiated study strategy and governance to address key scientific gaps.
  • Partner with Clinical Development to integrate evidence generation plans across development phases and support regulatory interactions.
  • Collaborate with Regulatory, Commercial, Market Access, and Patient Advocacy teams to align evidence plans with stakeholder needs.
  • Establish and maintain relationships with key opinion leaders, academic investigators, and patient organizations.
  • Represent BridgeBio at scientific congresses, advisory boards, and external forums.
  • Oversee evidence dissemination through publications and congress presentations, and serve as medical reviewer and approver for relevant materials.

Requirements

  • MD, DO, PharmD, PhD, or equivalent advanced scientific or clinical degree.
  • 10+ years of experience in Medical Affairs, Clinical Development, HEOR, or Evidence Generation roles within biopharmaceutical industry and/or academic medicine.
  • Demonstrated experience leading integrated evidence generation strategy in rare disease strongly preferred.
  • Experience in skeletal disorders, endocrinology, rare genetic diseases, or metabolic bone disease preferred.
  • Proven expertise in real-world evidence, registries, HEOR, and Phase 4 study design and execution.
  • Experience supporting late-stage development, launch preparation, and post-marketing medical activities.
  • Strong understanding of regulatory and compliance requirements related to medical research and post-marketing studies.
  • Demonstrated ability to lead cross-functional teams in a matrixed, fast-paced environment.
  • Excellent written and verbal communication skills, including presenting to senior leadership and external stakeholders.
  • Ability to travel up to 30–40% domestically and internationally; occasional evening and weekend work may be required.

Benefits

  • Market-leading compensation with an anticipated salary range of $270,000 to $375,000 USD for California-based candidates.
  • Annual performance bonus and company equity.
  • 401(k) with employer match.
  • Employee Stock Purchase Program (ESPP).
  • Pre-tax commuter benefits for transit and parking.
  • Referral bonus for hired candidates.
  • 100% employer-paid medical, dental, and vision premiums for employees and dependents.
  • Health Savings Account with annual employer contributions and Flexible Spending Accounts.
  • Fertility and family-forming benefits.
  • Expanded mental health support, including therapy and coaching resources.
  • Hybrid work model with flexibility; remote or hybrid/on-site in San Francisco.
  • Flexible, take-what-you-need paid time off plus company-paid holidays.
  • Comprehensive paid medical and parental leave.
  • Professional development resources through LinkedIn Learning, LifeLabs, and BetterUp Coaching.

Interested in this position?

Apply directly on the company website

Apply Now

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