Senior Clinical Trial Manager- Imaging Study

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.

What You'll Do

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

Responsibilities

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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.

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Manage external vendors and contract research organizations, may manage internal resources such as Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs)

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Prepare/Review/Approve study documents such as the Monitoring Manual, Study Operational Manual, Source Data Verifications Plan, and Laboratory Manual

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Coordinate and design study materials such as CRFs, patient diaries, study participation cards, and source documents.

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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

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Negotiate and mange vendor work agreements an site contracts

Where You'll Work

This is a U.S.based remote role that will require quarterly, or as needed visits to our San Francisco Office.

Who You Are

Historically the "Experience, Education, & Skills Requirement" section

(5-7 bullets max)

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Bachelor’s degree in a scientific discipline or equivalent is required, and an advanced degree

is preferred

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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

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Must have vendor management experience in clinical operations/development

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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

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Ability to build and maintain strong working relationships within the department and cross- functionally to meet a project or corporate goal

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Experience with Microsoft Office Suite required (Word, Excel, Project, Outlook)

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Must be able and willing to travel periodically

Rewarding Those Who Make the Mission Possible

We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

Financial Benefits:

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Market leading compensation

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401K with 100% employer match on first 3% & 50% on the next 2%

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Employee stock purchase program

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Pre-tax commuter benefits

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Referral program with $2,500 award for hired referrals

Health & Wellbeing:

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Comprehensive health care with 100% premiums covered - no cost to you and dependents

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Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions)

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Hybrid work model - employees have the autonomy in where and how they do their work

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Unlimited flexible paid time off - take the time that you need

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Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents

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Flex spending accounts & company-provided group term life & disability

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Subsidized lunch via Forkable on days worked from our office

Skill Development & Career Paths:

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People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility

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We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching

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We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities

#LI-NT1

At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.

Salary
$162,700—$191,000 USD