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Syneos Health

Senior Project Manager – Full Service

Syneos Health

. Provide customer-focused leadership in managing and delivering operational, financial, and strategic aspects of clinical research projects from proposal development through final deliverables .

Posted 9/18/2026full-timeRemote • United States, CanadaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical research projects, ensuring compliance with GCP and ICH guidelines, while effectively leading cross-functional teams and maintaining strong client relationships. Proven ability to oversee project budgets, timelines, and deliverables in a fast-paced environment.

Highest-signal resume keywords
Clinical Research ManagementGCP ComplianceCross-Functional Team LeadershipProject Budget ManagementClient Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ManagementProject BudgetingTimeline ManagementRisk MitigationStudy ExecutionRegulatory ComplianceProject ReportingFinancial Performance MonitoringProposal DevelopmentTrial Master File Oversight
Soft Skills
Excellent CommunicationInterpersonal SkillsLeadership SkillsPresentation SkillsMentoring
Tools & Technologies
Tracking ToolsReporting SystemsProject Management Software
Industry Keywords
Clinical Research OrganizationLife SciencesMedicineNursingPharmacyICH GuidelinesRegulatory RequirementsClinical Development Process

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide customer-focused leadership in managing and delivering operational, financial, and strategic aspects of clinical research projects from proposal development through final deliverables
  • Oversee studies ranging from single-service programs to large-scale, full-service global clinical trials across multiple phases and therapeutic areas
  • Serve as the primary client contact and lead cross-functional teams
  • Independently manage clinical studies from startup through closeout
  • Lead operational and financial execution of Phase II and III clinical trials, including global and multi-protocol studies
  • Act as liaison between sponsors and internal project teams
  • Ensure studies comply with GCP, ICH guidelines, regulatory requirements, and company SOPs
  • Oversee project timelines, budgets, resources, risks, and deliverables
  • Drive day-to-day study execution and resolve project issues
  • Coordinate activities across functional teams and external partners
  • Maintain accountability for project quality, financial performance, and customer satisfaction
  • Build and maintain relationships with sponsors and key stakeholders
  • Lead client meetings and provide regular project updates
  • Prepare and present project materials for internal and external meetings
  • Participate in bid defense meetings and business development activities
  • Support client growth opportunities through project delivery and relationship management
  • Manage project budgets, forecasting, and financial performance
  • Monitor project progress using timelines, metrics, tracking tools, and reporting systems
  • Develop risk mitigation and contingency plans
  • Ensure inspection readiness, including oversight of Trial Master Files and project documentation
  • Prepare project reports for sponsors and senior leadership
  • Lead and motivate cross-functional project teams
  • Mentor junior Project Managers and Project Support staff
  • Facilitate project-specific and therapeutic area training

Requirements

What you’ll need
  • Minimum Bachelor's degree in Life Sciences, Medicine, Nursing, Pharmacy, or a related discipline, or equivalent combination of Bachelor’s degree and experience
  • Clinical Research Organization (CRO) experience required
  • Proven experience independently managing clinical trials from initiation through closeout
  • Strong hands-on cross-functional project management experience with direct involvement in study execution
  • Experience independently managing project budgets, timelines, resources, and client relationships
  • Strong knowledge of GCP, ICH Guidelines, regulatory requirements, and the clinical development process
  • Excellent communication, presentation, interpersonal, and leadership skills
  • Ability to work independently while managing multiple priorities in a fast-paced environment
  • Willingness to travel up to approximately 25%

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • Total Self culture
  • Company car or car allowance
  • Medical, dental, and vision health benefits
  • Company match 401(k)
  • 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