Lead clinical study teams to achieve key milestones in innovative studies aimed at developing life-changing medicines for patients with unmet needs.
Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
The Senior Clinical Trial Manager is responsible for the execution and management of assigned clinical studies while ensuring Good Clinical Practices (GCP) Compliance, high study quality, and timely completion. This position is responsible for assisting in meeting functional, organizational, and corporate goals for acoramidis (AG10) by providing successful management of clinical study teams and clinical trials
Leads the Clinical Study Team for assigned projects; may lead one or more clinical studies, from concept to protocol, and achieve corporate objectives and key milestones such as First Patient In, Interim Analysis, Database lock, etc.
Manage external vendors and contract research organizations, may manage internal resources such as Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs)
Prepare/Review/Approve study documents such as the Monitoring Manual, Study Operational Manual, Source Data Verifications Plan, and Laboratory Manual
Coordinate and design study materials such as CRFs, patient diaries, study participation cards, and source documents.
Manage operational activities at the study level and monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to GCP, Standard Operating Procedures (SOPs), and study
protocols
Negotiate and mange vendor work agreements an site contracts
This is a U.S.based remote role that will require quarterly, or as needed visits to our San Francisco Office.
Historically the "Experience, Education, & Skills Requirement" section
(5-7 bullets max)
Bachelor’s degree in a scientific discipline or equivalent is required, and an advanced degree
is preferred
Requires at least eight years of biopharma industry experience (relevant clinical trials experience, in the biotechnology, pharmaceutical, CRO, medical device industry) with at least two years managing clinical trials
Must have vendor management experience in clinical operations/development
Strong verbal and written communication skills, can communicate strategic direction and relevant context so that employees at all levels understand their role in achieving success
Ability to build and maintain strong working relationships within the department and cross- functionally to meet a project or corporate goal
Experience with Microsoft Office Suite required (Word, Excel, Project, Outlook)
Must be able and willing to travel periodically
#LI-NT1
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
Health & Well-Being
Skill Development & Career Paths:
Education Stipend
Regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
Equity Compensation
Employee Stock Purchase Program (ESPP)
Flexible Work Hours
Hybrid work model with flexibility
Health Insurance
100% employer-paid medical, dental, and vision premiums for you and your dependents
Other Benefit
Pre-tax commuter benefits (transit and parking)
Paid Time Off
Flexible, 'take-what-you-need' paid time off and company-paid holidays
Wellness Stipend
Expanded mental health support (therapy and coaching resources)
BridgeBio Pharma is a biopharmaceutical company focused on discovering and delivering transformative medicines for genetic diseases and genetically defined cancers. Utilizing a 'moneyball for biotech' approach, we minimize risk and drive innovation through small expert teams, creating a robust portfolio of over 20 drug development programs to address unmet medical needs.
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Clinical Trial Manager Q&A's