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Senior Global Project Manager – Immunology, Metabolic, Oncology
Syneos HealthSenior project manager leading global Phase II and III clinical trials for Syneos Health, a life sciences services company. Driving trial strategy, execution, compliance, and closeout across immunology, metabolic, and oncology programs.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading global Phase II and III clinical trials, with a strong focus on project management, regulatory compliance, and stakeholder engagement. Capable of developing and executing comprehensive trial strategies while ensuring alignment across diverse teams and cultures.
Highest-signal resume keywords
Global Clinical Trial LeadershipProject ManagementRegulatory ComplianceStakeholder ManagementRisk Mitigation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Global Clinical Trial PlanningPhase II Clinical TrialsPhase III Clinical TrialsRegulatory Landscape UnderstandingData CleaningDatabase LockTrial Closeout ActivitiesTrial Master File ManagementVendor Outsourcing StrategyBiomarker Coordination
Soft Skills
Exceptional LeadershipCommunication SkillsStakeholder ManagementCultural AttunementDiplomatic Communication
Certifications & Qualifications
Bachelor’s Degree
Industry Keywords
ImmunologyMetabolicOncologyGCPSOPsPatient-Focused OutcomesGlobal Site StrategiesFeasibility AssessmentsCross-Functional CoordinationScientific Publications
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Lead global planning activities and operational feasibility assessments for Phase II and III clinical trials
- Guide country allocation and feasibility processes and shape global site strategies
- Develop global engagement, recruitment, and risk mitigation plans
- Lead vendor outsourcing strategy, including identification, evaluation, and scope-of-work development
- Harmonize trial processes across clinical quality, safety, investigational product management, and financial planning
- Prepare or support responses to regulatory and ethics authorities across regions
- Ensure global teams are trained, aligned, and equipped for execution
- Oversee worldwide trial operations for compliance with GCP, SOPs, and regional regulations
- Monitor patient recruitment, risks, timelines, and budgets and drive issue resolution
- Direct documentation changes, study amendments, and retraining
- Oversee global vendors, central labs, and external partners
- Coordinate biomarker, genomic, and sub-study activities
- Lead data cleaning, database lock, and trial closeout activities
- Support CTR development, registry disclosure, scientific publications, and global study communications
- Ensure completeness and accuracy of the Trial Master File across participating regions
- Provide operational and scientific insight for global study strategy
- Lead or contribute to global feasibility assessments influencing trial design and regional planning
Requirements
What you’ll need- Required Bachelor’s degree (4-year undergraduate degree)
- Extensive project management experience leading global Phase II and III clinical trials
- Proven experience providing global leadership across Phase II and III clinical trials
- Experience in Immunology, Metabolic, or Oncology
- Deep understanding of global clinical trial planning, execution, and regulatory landscapes
- Exceptional leadership, communication, and stakeholder management skills across complex, matrixed, multicultural environments
- Ability to lead through influence, anticipate global challenges, and ensure patient-focused outcomes
- Expertise in global timelines, risk mitigation, cross-functional coordination, issue escalation, and solution delivery
- Ability to guide teams across regions, cultures, and functions
- Transparent, diplomatic, and culturally attuned communication skills
Benefits
Comp & perks- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Inclusive culture
- Company car or car allowance
- Medical, Dental and Vision health benefits
- 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)
- Sick time
- Reasonable accommodations, when appropriate