Clinical Trial Manager
Advanced Group · Redwood City, CA
CONTRACT
Posted Aug 11, 2026
Job Description
Clinical Trial Manager (CTM) – Clinical Operations (Open for candidates willing to relocate)
We are seeking an experienced Clinical Trial Manager (CTM) to join a dynamic Clinical Operations team. This role will independently manage one or more Phase 1–3 clinical studies or complex components of larger trials, with responsibility for study execution, CRO/vendor oversight, and cross-functional coordination.
Key Responsibilities:
• Manage clinical trial activities from study start-up through closeout
• Drive site activation, document readiness, enrollment tracking, and study milestones
• Manage CROs and clinical vendors, ensuring timely delivery of study activities
• Lead and participate in cross-functional and external study meetings
• Oversee TMF reconciliation and inspection readiness activities
• Review protocols, ICFs, CRFs, monitoring plans, and other study documents
• Monitor study metrics, identify trends, escalate risks, and support issue resolution
• Support clinical data review and preparation of interim/final Clinical Study Reports
• Contribute to process improvement initiatives within Clinical Operations
• Provide guidance and mentorship to junior Clinical Operations team members
Qualifications:
• Bachelor’s degree in a relevant scientific discipline, or equivalent experience
• 5–7+ years of experience in Clinical Operations or Clinical Research within the pharmaceutical/biotechnology industry
• Demonstrated experience managing Phase 1–3 clinical trials
• Strong knowledge of FDA/EMA regulations, ICH-GCP, and clinical research standards
• Experience with CRO and vendor management
• Familiarity with eTMF, EDC, IRT, and CTMS systems
• Strong organizational, communication, problem-solving, and decision-making skills
• Experience working on global clinical trials preferred
• Oncology experience strongly preferred
• Ability to manage multiple priorities and work effectively within cross-functional teams
• Approximately 15% travel may be required
Why Consider This Opportunity?
This is an excellent opportunity for an experienced Clinical Trial Manager to take ownership of complex clinical studies, collaborate with cross-functional teams and external partners, and contribute directly to successful clinical trial execution.
Interested?
Apply today or reach out to learn more about this opportunity.
We are seeking an experienced Clinical Trial Manager (CTM) to join a dynamic Clinical Operations team. This role will independently manage one or more Phase 1–3 clinical studies or complex components of larger trials, with responsibility for study execution, CRO/vendor oversight, and cross-functional coordination.
Key Responsibilities:
• Manage clinical trial activities from study start-up through closeout
• Drive site activation, document readiness, enrollment tracking, and study milestones
• Manage CROs and clinical vendors, ensuring timely delivery of study activities
• Lead and participate in cross-functional and external study meetings
• Oversee TMF reconciliation and inspection readiness activities
• Review protocols, ICFs, CRFs, monitoring plans, and other study documents
• Monitor study metrics, identify trends, escalate risks, and support issue resolution
• Support clinical data review and preparation of interim/final Clinical Study Reports
• Contribute to process improvement initiatives within Clinical Operations
• Provide guidance and mentorship to junior Clinical Operations team members
Qualifications:
• Bachelor’s degree in a relevant scientific discipline, or equivalent experience
• 5–7+ years of experience in Clinical Operations or Clinical Research within the pharmaceutical/biotechnology industry
• Demonstrated experience managing Phase 1–3 clinical trials
• Strong knowledge of FDA/EMA regulations, ICH-GCP, and clinical research standards
• Experience with CRO and vendor management
• Familiarity with eTMF, EDC, IRT, and CTMS systems
• Strong organizational, communication, problem-solving, and decision-making skills
• Experience working on global clinical trials preferred
• Oncology experience strongly preferred
• Ability to manage multiple priorities and work effectively within cross-functional teams
• Approximately 15% travel may be required
Why Consider This Opportunity?
This is an excellent opportunity for an experienced Clinical Trial Manager to take ownership of complex clinical studies, collaborate with cross-functional teams and external partners, and contribute directly to successful clinical trial execution.
Interested?
Apply today or reach out to learn more about this opportunity.
Additional Details
- City
- Redwood City
- State
- California
- Country
- US
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