BridgeBio Pharma

Biopharma

Sr.ClinicalTrialManager

$0–0k United States Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Sr. Clinical Trial Manager at BridgeBio Pharma. Skills: Clinical trial management, Vendor management, Protocol development. Manage clinical studies. Achieve corporate objectives”

What You'll Achieve.

achieve corporate objectives and key milestones such as First Patient In, Interim Analysis, Database lock

Industry & Context.

Biopharma
Problems you'll solve

empower people to solve problems

Eligibility Requirements

require quarterly, or as needed visits to our San Francisco Office, able and willing to travel periodically

What They're Looking For.

Must Have

Bachelor’s degree in a scientific discipline or equivalent, at least eight years of biopharma industry experience, at least two years managing clinical trials, vendor management experience in clinical operations/development, verbal and written communication skills, Ability to build and maintain working relationships, Experience with Microsoft Office Suite

Nice to Have

advanced degree

What You'll Do.

Manage clinical studies

Achieve corporate objectives

Manage external vendors

Manage internal resources

Prepare study documents

Coordinate study materials

Manage operational activities

Manage monitoring activities

Negotiate vendor agreements

Manage site contracts

How You'll Work.

Team & Collaboration

build and maintain working relationships within the department and cross-functionally

Communication Scope

verbal and written communication skills; communicate strategic direction and relevant context

Process & Methodology

Manage clinical studies from concept to protocol, Achieve corporate objectives and key milestones

Full Job Description

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 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 Where You'll Work This is a U.S.based remote role that will require quarterly, or as needed visits to our San Francisc

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