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ICON plc

Vendor Start up Manager – eCOA

ICON plc

. Review vendor and category-specific protocol requirements and incorporate supplier expertise into final study specifications .

Posted 10/27/2026full-timeRemote • United Kingdom, Bulgaria, Poland, Belgium, Netherlands, Italy, SpainMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in vendor management and oversight within clinical operations, with a strong understanding of GxP, ICH-GCP, and regulatory requirements. Proven ability to lead User Acceptance Testing (UAT) for systems such as eCOA and IRT while effectively communicating with stakeholders.

Highest-signal resume keywords
Vendor ManagementUser Acceptance Testing (UAT)Clinical Trial DesignGxP and ICH-GCP ComplianceVendor Selection and Procurement

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 OperationsVendor OversightBudget AssessmentRoot-Cause AnalysisStudy Specification DevelopmentRegulatory SubmissionsPerformance MonitoringContract NegotiationRisk Mitigation PlanningStudy Start-Up Activities
Soft Skills
Effective CommunicationStakeholder CollaborationPartnership BuildingProblem-SolvingFacilitation
Tools & Technologies
ECOAIRTVendor Management ToolsStudy Specification Worksheets
Industry Keywords
Clinical TrialsGxPICH-GCPVendor CategoriesCentral LaboratoriesPatient Recruitment and Retention (PR&R)Procurement ProcessesRFPsRFQs

About the role

Key responsibilities & impact
  • Review vendor and category-specific protocol requirements and incorporate supplier expertise into final study specifications
  • Support development of Study Specification Worksheets (SSWs) for vendor selection and bidding
  • Partner with Procurement and vendors to evaluate proposals and quotations and support contract discussions
  • Assess and validate vendor budgets against project scope and quotations
  • Organise vendor kick-off meetings and facilitate vendor governance discussions throughout the study lifecycle
  • Coordinate collection and submission of vendor documentation for regulatory authority submissions
  • Lead User Acceptance Testing (UAT) for systems such as eCOA and IRT
  • Communicate protocol amendments and study design changes to vendors and update budgets, timelines, and service agreements
  • Drive study start-up activities supporting timely vendor database deployment and operational readiness
  • Oversee vendor performance against quality, timeline, and service standards
  • Identify vendor risks and develop mitigation and contingency plans
  • Monitor performance issues, implement corrective actions, and escalate concerns
  • Conduct root-cause analysis and identify supplier performance trends
  • Contribute to vendor management processes, templates, tools, and best practices

Requirements

What you’ll need
  • Advanced degree in a scientific, life sciences, or business-related discipline, or equivalent industry experience
  • Fluent in written and spoken English
  • 3+ years of experience within clinical operations, with strong expertise in vendor management and oversight
  • Solid understanding of GxP, ICH-GCP, and applicable regulatory requirements
  • In-depth knowledge of clinical trial design and translating study requirements into vendor deliverables
  • Strong understanding of supplier-provided clinical services and associated operational specifications
  • Demonstrated experience managing vendor relationships and collaborating with external service providers
  • Proven ability to build effective partnerships with internal and external stakeholders
  • Experience leading or supporting User Acceptance Testing (UAT), particularly for eCOA and IRT platforms
  • Understanding of study start-up milestones, vendor readiness activities, and critical path deliverables
  • Experience supporting outsourcing, vendor selection, contracting, and procurement processes, including RFPs and RFQs
  • Expertise in one or more clinical vendor categories, such as Central Laboratories, eCOA/ePRO, IRT, Imaging, Cardiac and Respiratory Diagnostics, or Patient Recruitment and Retention (PR&R)
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways