Senior Manager / Associate Director, Medical Information
About The Position
The Senior Manager / Associate Director, Medical Information will support execution of the Medical Information function for BridgeBio’s Skeletal Dysplasia program, infigratinib. Reporting to the Director, Medical Information, this hands-on content and operational lead will develop, review, and maintain accurate, high-quality, compliant medical information for internal and external stakeholders. The role works across Medical Affairs, Clinical Development, Regulatory, Pharmacovigilance, Commercial, and external vendors to deliver consistent scientific exchange tailored to the condition, program stage, and stakeholder needs. This U.S.-based remote role may require quarterly or as-needed visits to the San Francisco office or other locations for key internal meetings. The anticipated California salary range is $165,000–$210,000, with the final offer dependent on factors including experience, education, location, and interview performance. BridgeBio offers a market-competitive total rewards package that includes base pay, annual performance bonus, company equity, and benefits.
Requirements
- Advanced degree: MD, PharmD, PhD, or equivalent scientific degree.
- At least 3 years of Medical Information and/or Medical Affairs experience in biotechnology or pharmaceutical settings for the Senior Manager level, or at least 5 years for the Associate Director level.
- For the Senior Manager level, completion of a Medical Information or Medical Affairs fellowship may also be considered.
- Demonstrated experience developing high-quality Medical Information content, including standard and custom response letters and FAQs.
- Experience supporting Medical Information operations, including vendor oversight and inquiry quality review.
- Working knowledge of Medical Information compliance, regulations, and industry best practices, including medical review processes.
- Strong written and verbal communication skills, including the ability to translate complex clinical data into clear, balanced responses.
- Strong cross-functional collaboration skills and ability to work effectively in a fast-paced, matrixed, evolving organization.
- Scientific curiosity, attention to detail, and commitment to patient-focused medical excellence.
Nice To Haves
- Experience in rare disease.
- Prior experience in a lean, growing biotech environment.
Responsibilities
- Support development and execution of the Medical Information strategy for infigratinib in alignment with Medical Affairs and program objectives.
- Serve as the day-to-day Medical Information lead and subject matter expert for infigratinib, maintaining knowledge of the condition, product, and competitive landscape.
- Author, review, and maintain medical information materials, including standard response letters, FAQs, and custom response letters for escalated inquiries.
- Ensure content is scientifically accurate, medically rigorous, consistent, and compliant with applicable regulations, company policies, and industry standards.
- Conduct ongoing literature surveillance and work with Clinical and Translational teams to incorporate current data and insights.
- Implement and refine SOPs, workflows, and quality controls for inquiry intake, response, documentation, and reporting.
- Partner with Pharmacovigilance on appropriate adverse event and product complaint reporting.
- Support management of external Medical Information vendors, including defining scope, training, reviewing inquiry-handling quality, and monitoring performance metrics.
- Oversee daily intake and response to unsolicited medical inquiries from healthcare professionals, patients, and other stakeholders.
- Represent Medical Information on medical, legal, and regulatory review committees as appropriate, and support Medical Information presence at scientific congresses.
- Collaborate with Field Medical, Publications, Commercial, and Patient Advocacy teams to align scientific messaging and stakeholder experience.
- Support scientific communication activities with Medical Affairs and Publications.
- Analyze and report inquiry metrics and trends, and present insights to inform medical strategy, evidence generation, and educational initiatives.
- Contribute to evaluating and implementing tools and technologies, including AI-enabled solutions, to improve Medical Information process efficiency and quality.
- Support readiness for new data, indications, and lifecycle milestones, including development of timely Medical Information resources.
Benefits
- Annual performance bonus
- 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
- Subsidized lunch and parking on in-office days
- 100% employer-paid medical, dental, and vision premiums for employees and dependents
- Health Savings Account with annual employer contributions
- Flexible Spending Accounts
- Fertility and family-forming benefits
- Expanded mental health support, including therapy and coaching resources
- Flexible, take-what-you-need paid time off
- Company-paid holidays
- Paid medical and parental leave
- Continuous education and professional development programs
- LinkedIn Learning, LifeLabs, and BetterUp Coaching
- Financial rewards, peer-to-peer recognition, and growth opportunities
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree
