Clinical Trial Manager, Senior

BBOT

Clinical Trial Manager overseeing execution of oncology clinical trials for BridgeBio Oncology Therapeutics. Focused on ensuring adherence to timelines, budgets, and quality standards.

Posted 7/3/2026full-timeRemote • 🏈 Anywhere in North AmericaSenior💰 $140,000 - $180,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the Director in overseeing global clinical trial execution, including site activation, enrollment, monitoring, and closeout
Support the Director in leading cross functional trial team meetings and ensure alignment on key deliverables, timelines, and risk mitigation strategies
Manage day-to-day operational activities for assigned studies, ensuring adherence to timelines, budgets, and quality standards
Drive vendor integration strategies to ensure seamless execution between CRO, central labs, and any specialty service providers
Act as the main clinical operations point of contact for assigned study-level tasks, including managing CROs and vendors in collaboration with the Director
Ensure completeness and inspection-readiness of the trial master file (TMF/eTMF)
Support the development and maintenance of key operational documents including study manuals, ICFs, tracking tools, and monitoring plans
Participate in the conduct of audits and support regulatory inspections related to GCP
Monitor regulatory and GCP compliance across trial activities and support audit/inspection readiness
Review clinical trial data listings to support identification and resolution of protocol deviations, data trends, and outstanding queries
Own CRO and vendor oversight by tracking deliverables, proactively identifying risks until issue resolution, and performance metrics in partnership with the Program/Study Lead
Oversee lab sample management processes, including sample tracking, shipment, reconciliation, and vendor coordination to ensure timely and compliant handling of biological specimens
Contributes to continuous process improvement and SOP development
Participate in team meetings, providing clinical operations insights and updates to internal stakeholders

Requirements

What you’ll need

Bachelor’s degree in life sciences or related field
Minimum 4 years of experience in Clinical Operations, working with CROs and other vendors
Strong understanding of CRO/vendor oversight and clinical development process
Early-phase oncology experience preferred
Prior experience in a lean or startup environment is highly desirable
Excellent project management, communication, and problem-solving skills
Working knowledge of ICH-GCP and global regulatory requirements
Proficient in clinical trial systems (e.g., EDC, CTMS, eTMF) and Microsoft Office Suite

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account BBOT Website LinkedIn All Job Openings 51 - 200 employees 🧬 Biotechnology 💊 Pharmaceuticals Biotechnology
Pharmaceuticals BBOT is a biotechnology company developing targeted therapies for cancers driven by RAS signaling and PI3Kα. The company focuses on rational drug design to inhibit the active ON state of RAS and to selectively block RAS-driven PI3K activation, aiming at multiple KRAS mutants and novel approaches to maximize target inhibition. BBOT translates decades of RAS biology research into therapeutic candidates intended to improve outcomes for patients with RAS- and PI3Kα-driven tumors. Clinical Trial Manager, Senior 🔥 29 minutes ago 🏈 North America – Remote 💵 $140k - $180k / year ⏰ Full Time 🟠 Senior 🧪 Clinical Research Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Support the Director in overseeing global clinical trial execution, including site activation, enrollment, monitoring, and closeout
Support the Director in leading cross functional trial team meetings and ensure alignment on key deliverables, timelines, and risk mitigation strategies
Manage day-to-day operational activities for assigned studies, ensuring adherence to timelines, budgets, and quality standards
Drive vendor integration strategies to ensure seamless execution between CRO, central labs, and any specialty service providers
Act as the main clinical operations point of contact for assigned study-level tasks, including managing CROs and vendors in collaboration with the Director
Ensure completeness and inspection-readiness of the trial master file (TMF/eTMF)
Support the development and maintenance of key operational documents including study manuals, ICFs, tracking tools, and monitoring plans
Participate in the conduct of audits and support regulatory inspections related to GCP
Monitor regulatory and GCP compliance across trial activities and support audit/inspection readiness
Review clinical trial data listings to support identification and resolution of protocol deviations, data trends, and outstanding queries
Own CRO and vendor oversight by tracking deliverables, proactively identifying risks until issue resolution, and performance metrics in partnership with the Program/Study Lead
Oversee lab sample management processes, including sample tracking, shipment, reconciliation, and vendor coordination to ensure timely and compliant handling of biological specimens
Contributes to continuous process improvement and SOP development
Participate in team meetings, providing clinical operations insights and updates to internal stakeholders 🎯 Requirements
Bachelor’s degree in life sciences or related field
Minimum 4 years of experience in Clinical Operations, working with CROs and other vendors
Strong understanding of CRO/vendor oversight and clinical development process
Early-phase oncology experience preferred
Prior experience in a lean or startup environment is highly desirable
Excellent project management, communication, and problem-solving skills
Working knowledge of ICH-GCP and global regulatory requirements
Proficient in clinical trial systems (e.g., EDC, CTMS, eTMF) and Microsoft Office Suite Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Find jobs using your resume Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

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Hard Skills & Tools

Clinical Trial ManagementRegulatory ComplianceData AnalysisProtocol Deviation ResolutionOperational Document Development

Soft Skills

CommunicationProblem-SolvingTeam CollaborationLeadership