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ICON plc

Clinical Trial Manager – Regulatory Submissions

ICON plc

. Lead the preparation and submission of essential documents for regulatory approvals and site activation .

Posted 10/7/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical study start-up activities, regulatory compliance, and project management, with a strong focus on collaboration and quality assurance. Proven ability to lead teams and streamline processes to enhance operational efficiency in clinical research.

Highest-signal resume keywords
Study Start-Up ActivitiesRegulatory ComplianceProject ManagementOrganizational SkillsCommunication Skills

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
Regulatory ApprovalsSite ActivationClinical ResearchProject PrioritizationQuality Assurance
Soft Skills
Interpersonal SkillsCollaborationAttention to Detail
Industry Keywords
Clinical OperationsCompliance StandardsStudy TeamsIndustry RegulationsHealthcare-Related Field

About the role

Key responsibilities & impact
  • Lead the preparation and submission of essential documents for regulatory approvals and site activation
  • Collaborate with project management, clinical operations, and regulatory affairs to streamline study start-up processes
  • Oversee the identification and selection of clinical sites, ensuring they meet project criteria and compliance standards
  • Provide guidance and support to study teams and sites during the start-up phase
  • Stay current with industry regulations and trends to enhance start-up strategies and best practices
  • Coordinate site start-up and activation delivery, resolve issues, and develop team capability

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in study start-up activities within the clinical research industry, with a strong understanding of regulatory requirements
  • Proven ability to manage multiple projects and prioritize tasks effectively in a fast-paced environment
  • Excellent organizational skills and attention to detail, with a commitment to delivering high-quality results
  • Strong communication and interpersonal skills, enabling effective collaboration with diverse teams and external stakeholders
  • A commitment to maintaining high standards of quality and compliance in all study start-up activities
  • 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