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ICON plc

Site Activation Lead

ICON plc

. Lead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution .

Posted 10/5/2026full-timeRemote • ItalySenior💰 €45,040 - €56,300 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading clinical trial start-up activities and managing site activation processes while ensuring compliance with regulatory standards and client objectives. Strong project management capabilities are essential for optimizing performance and achieving successful study outcomes.

Highest-signal resume keywords
Clinical Research ExperienceProject Management SkillsRegulatory KnowledgeSite Activation PlanningCommunication Abilities

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 Start-UpSite ActivationRegulatory ProcessesProject ManagementStudy Planning
Soft Skills
Excellent CommunicationTime ManagementCollaboration
Industry Keywords
Life SciencesSOPsKPISponsor ExpectationsBid Defenses

About the role

Key responsibilities & impact
  • Lead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution
  • Oversee day-to-day delivery of all aspects of site activation in assigned projects, ensuring adherence to sponsor timelines, expectations, ICON/client KPIs, SOPs, and regulatory standards
  • Ensure each project has a comprehensive site activation plan and conduct studies in accordance with the plan
  • Lead sponsor initiatives such as kick-off meetings, bid defenses, project updates, status calls, and other key communications
  • Use project management skills to optimize performance and collaboration and ensure successful study outcomes
  • Manage day-to-day site start-up and activation activities and support the team in delivering quality outcomes

Requirements

What you’ll need
  • Bachelor's Degree, preferably in life sciences
  • Minimum of 4 years of experience in a Clinical Research environment, focusing on Start-Up experience
  • Strong project management skills
  • Deep understanding of regulatory and submission processes in various countries
  • Excellent written and verbal communication abilities
  • Proven ability to work efficiently to tight deadlines and manage multiple priorities
  • Willingness to travel as required (approximately 15%)
  • 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