Senior Manager, Medical Affairs — Remote

BridgeBio Pharma; United States; Remote; USD 165,000 - 210,000; Full time

Benefits offered by this job

Market-leading compensation

401(k) with employer match

Employee Stock Purchase Program (ESPP)

Pre-tax commuter benefits

Hybrid work model

PTO and holidays

Insurance premiums for dependents

Job summary

BridgeBio Pharma seeks a Sr. Manager/Associate Director, Medical Affairs, to lead medical review, MLR submissions, content creation, and advisory board activities across skeletal dysplasia programs. The role is remote in the USA with potential in-person collaboration and travel.

You will work with Medical Directors and cross-functional teams to advance scientific communications, data analyses, and external collaborations while ensuring compliance and high-quality deliverables.

Qualifications

• 3–5 years pharma/biotech Medical Affairs experience with medical review and MLR submissions.
• Experience developing scientific content and executing advisory boards or symposia.
• Strong project-management and organizational skills with multiple workstreams.

Responsibilities

• Review scientific and medical materials; ensure accuracy and alignment with source data.
• Lead MLR submissions and track through final approval.
• Collaborate with Medical Information to develop updated response materials.
• Manage advisory boards: coordination, materials, timelines, and post-meeting deliverables.
• Support development and execution of company-sponsored scientific symposia and post-event analyses.

Skills

Medical affairs

Project management

Scientific writing

Advisory boards

KOL engagement

Education

PharmD

PhD

Genetic counseling degree

NP/Advanced practice degree

MS

Job description

BridgeBio Pharma seeks a Sr. Manager/Associate Director, Medical Affairs, to lead medical review, MLR submissions, content creation, and advisory board activities across skeletal dysplasia programs. The role is remote in the USA with potential in-person collaboration and travel.

You will work with Medical Directors and cross-functional teams to advance scientific communications, data analyses, and external collaborations while ensuring compliance and high-quality deliverables.