BridgeBio Pharma

SR. Trial Master File Specialist

BridgeBio Pharma

22 hours ago
United States
Onsite
Full Time
Medior
0 applicants
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BridgeBio Pharma
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About this role

The Clinical Trial Master File Specialist manages and oversees the documentation and quality control of trial master files for clinical studies, ensuring compliance with regulatory standards and inspection readiness. They support clinical trial teams throughout the study lifecycle and contribute to process improvements.

Skills

Qualifications

Bachelor's degree in life sciences, health sciences, or related field2-5+ years of experience in clinical trials or TMF management
BridgeBio Pharma

About BridgeBio Pharma

bridgebio.com

BridgeBio is a biotechnology company designing transformative medicines for patients with genetic diseases and cancers driven by clear genetic causes. The company advances programs from target discovery through clinical development, combining human genetics and translational science with rigorous clinical trials to create targeted therapeutics. BridgeBio builds a diversified portfolio of wholly owned and partnered programs across multiple modalities and uses a venture‑style operating model to accelerate and de‑risk development. Its mission is to translate genetic insights into precision medicines for patients with high unmet medical need.

About BridgeBio Pharma

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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