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Principal Site Activation Manager
Syneos Health. Lead and oversee global site activation activities from study start-up through site readiness .
Posted 10/22/2026full-timeMorrisville • North Carolina • United StatesLead💰 $97,300 - $170,300 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading global site activation activities, managing timelines, risks, and deliverables while ensuring compliance with regulatory requirements and sponsor expectations. Proven ability to collaborate with cross-functional teams and provide guidance to Site Activation Managers and study teams.
Highest-signal resume keywords
Global Site Activation LeadershipRegulatory Compliance ManagementTimeline and Risk ManagementCross-Functional CollaborationIssue Resolution Support
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Site Activation Strategy DevelopmentPerformance Metrics TrackingStudy Start-Up ManagementDeliverable ManagementSOP Compliance
Soft Skills
Guidance and OversightProblem-SolvingStakeholder Engagement
Industry Keywords
Clinical OperationsRegulatory AffairsContracts and BudgetsStudy TeamsActivation Milestones
About the role
Key responsibilities & impact- Lead and oversee global site activation activities from study start-up through site readiness
- Develop and execute country and site activation strategies
- Manage timelines, risks, and deliverables across multiple studies or programs
- Partner closely with Clinical Operations, Regulatory Affairs, Contracts & Budgets, and external stakeholders
- Drive performance metrics and ensure activation milestones are achieved
- Provide guidance and oversight to Site Activation Managers and study teams
- Support issue escalation and resolution for complex start-up challenges
- Ensure compliance with regulatory requirements, SOPs, and sponsor expectations
Requirements
What you’ll need- Equivalent experience, skills, and/or education will also be considered
- Compliance with regulatory requirements, SOPs, and sponsor expectations
- Ability to manage timelines, risks, and deliverables across multiple studies or programs
- Ability to partner with Clinical Operations, Regulatory Affairs, Contracts & Budgets, and external stakeholders
- Ability to provide guidance and oversight to Site Activation Managers and study teams
- Ability to support issue escalation and resolution for complex start-up challenges
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