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Clinical Trial Manager – Senior
BBOTClinical Trial Manager overseeing early-phase oncology trials with a focus on execution and vendor management. Collaborating closely with internal and external partners to deliver high-quality clinical data.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial execution, including site activation, enrollment, and monitoring, while ensuring compliance with ICH-GCP and regulatory standards. Proficient in managing CROs and vendors, with strong project management and communication skills to drive operational excellence.
Highest-signal resume keywords
Clinical Operations ManagementCRO/Vendor OversightProject ManagementRegulatory ComplianceClinical Trial Systems Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ExecutionSite ActivationEnrollment ManagementMonitoring and CloseoutGCP ComplianceData AnalysisProcess ImprovementSOP DevelopmentRisk MitigationOncology Experience
Soft Skills
CommunicationProblem-SolvingTeam CollaborationLeadership
Tools & Technologies
EDCCTMSETMFMicrosoft Office Suite
Industry Keywords
Clinical DevelopmentRegulatory InspectionsTrial Master FileLean EnvironmentBiological Specimen Management
Tech Stack
Tools & technologiesGoogle 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
- Participates 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 🔥 11 minutes ago 🇺🇸 United States – 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
- Participates 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 Similar Jobs Clinical Trial Manager 🔥 19 hours ago Syneos Health 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Clinical Trial Manager managing site oversight and monitoring deliverables for clinical trials. Collaborating across teams to ensure compliance and improve patient safety in clinical development. 🇺🇸 United States – Remote 💵 $114k - $210.9k / year ⏰ Full Time 🟡 Mid-level 🟠 Senior 🧪 Clinical Research 🦅 H1B Visa Sponsor Principal Biostatistician – Team Lead 🔥 22 hours ago Cleveland Clinic 10,000+ employees Website LinkedIn All Job Openings Principal Biostatistician Team Lead at Cleveland Clinic guiding biostatisticians and overseeing clinical trials. Collaborating with interdisciplinary teams to develop innovative research methodologies and manage projects. 🇺🇸 United States – Remote ⏰ Full Time 🟠 Senior 🧪 Clinical Research 🦅 H1B Visa Sponsor Clinical Scientist, Medical Monitoring – Oncology – Breast 🕒 3 days ago Syneos Health 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Clinical/Medical Scientist developing medical plans and ensuring quality deliverables in drug development processes. Collaborating with Medical Directors and study teams to maintain project timelines and data integrity. 🇺🇸 United States – Remote 💵 $67.7k - $115.1k / year ⏰ Full Time 🟡 Mid-level 🟠 Senior 🧪 Clinical Research 🦅 H1B Visa Sponsor Clinical/Medical Scientist – Oncology – Gynecologic Malignancies 🕒 3 days ago Syneos Health 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Clinical Scientist developing medical plans for oncology studies at Syneos Health. Collaborating with Medical Directors and engaging with experts to ensure data integrity and safety. 🇺🇸 United States – Remote 💵 $67.7k - $115.1k / year ⏰ Full Time 🟡 Mid-level 🟠 Senior 🧪 Clinical Research 🦅 H1B Visa Sponsor Senior Clinical Scientist – Medical Monitoring, Oncology – Breast 🕒 3 days ago Syneos Health 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Sr Clinical/Medical Scientist in Oncology at Syneos Health developing medical plans and conducting data reviews. Collaborate with cross-functional teams to ensure project deliverables. 🇺🇸 United States – Remote 💵 $79.8k - $139.6k / year ⏰ Full Time 🟠 Senior 🧪 Clinical Research 🦅 H1B Visa Sponsor View More Clinical Researcher Jobs 🌐 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