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Clinical Project Manager II – Early Phase Oncology
Syneos HealthClinical Project Manager II driving execution of Early Phase Oncology trials at Syneos Health. Managing all operational aspects and ensuring timely delivery of key milestones in a fast-paced team environment.
Posted 6/20/2026full-timeFoster City • California • 🇺🇸 United StatesMid-LevelSenior💰 $95,000 - $175,700 per yearWebsite
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Drive operational execution of Early Phase Oncology clinical trials from study start-up through database lock and closeout
- Independently manage day-to-day study operations with minimal oversight
- Own timelines, deliverables, risks, and issue resolution across multiple workstreams
- Maintain deep operational awareness across all aspects of the trial — this is a role for someone comfortable working "in the weeds"
- Ensure study milestones stay on track in a fast-paced environment with shifting priorities and competing demands
- Partner cross-functionally to proactively identify risks, remove roadblocks, and implement operational solutions quickly
- Support operational activities associated with dose escalation cohorts, dose expansion cohorts, safety review meetings, protocol amendments, enrollment management, and study execution activities
- Monitor enrollment, site performance, data quality, and operational metrics to support successful study execution
- Drive accountability across study teams to ensure timelines and deliverables are met
- Lead vendor management activities and maintain strong oversight of external partners and CROs
- Contribute to RFP development, vendor selection, and ongoing vendor performance management
- Hold vendors accountable to timelines, deliverables, quality expectations, and issue resolution
- Actively manage operational follow-through rather than relying solely on escalation pathways
- Partner closely with CROs, monitoring teams, central laboratories, imaging vendors, and specialty oncology service providers
- Lead cross-functional meetings with clear agendas, action-oriented discussions, and strong follow-up
- Drive accountability across internal teams and external partners
- Build strong collaborative relationships while effectively navigating challenging conversations and competing priorities
- Mentor or support junior team members as needed
- Operate confidently within a matrixed global environment with multiple stakeholders
- Draft, review, and coordinate key study documents including protocols, informed consents, monitoring plans, investigator brochures, clinical study reports, and other essential study documentation
- Support study budget tracking, forecasting, and operational planning activities
- Review data listings and support interim and final reporting activities
- Train CROs, investigators, study coordinators, and vendors on protocol and study requirements
- Support inspection readiness activities and maintain compliance with GCP, ICH, and applicable regulatory requirements
- Contribute to SOP development, process improvement initiatives, and operational best practices
Requirements
What you’ll need- 3+ years of Clinical Project Management experience within clinical research
- Experience independently managing clinical trials from study start-up through closeout
- Direct Oncology clinical trial experience
- Direct Early Phase Oncology clinical trial experience supporting Phase I, Phase Ib, and/or Phase II studies
- Strong understanding of the unique operational requirements associated with Early Phase Oncology programs
- Experience supporting dose escalation and/or dose expansion studies
- Strong CRO/vendor management and oversight experience
- Proven ability to independently drive study execution in fast-paced clinical environments
- Experience managing cross-functional clinical trial activities within matrixed organizations
- Comfortable balancing strategic oversight with hands-on operational execution
Benefits
Comp & perks- Health benefits to include Medical, Dental and Vision
- Company match 401k
- Eligibility to participate in Employee Stock Purchase Plan
- Eligibility to earn commissions/bonus based on company and individual performance
- Flexible paid time off (PTO) and sick time
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Clinical Project ManagementOncology clinical trialsEarly Phase Oncology trialsDose escalation studiesDose expansion studiesGCP complianceICH complianceOperational planningData quality monitoringVendor management
Soft Skills
LeadershipCollaborationProblem-solvingCommunicationMentoringAccountabilityAdaptabilityOrganizational skillsStakeholder managementConflict resolution