Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
ICON plc

Manager, Site Engagement

ICON plc

. Oversee scientific operations workstreams, ensuring deliverables meet quality and timeline expectations .

Posted 9/30/2026full-timeRemote • MexicoMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in site engagement and clinical operations, with a strong focus on regulatory compliance and quality deliverables. Proven ability to lead teams, manage site relationships, and enhance site performance in clinical trial settings.

Highest-signal resume keywords
Site Engagement ManagementClinical Operations LeadershipRegulatory Compliance (GCP)Project Management SkillsTeam Mentorship

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Site EngagementClinical OperationsRegulatory RequirementsProject ManagementProblem-SolvingOrganizational SkillsDetail-OrientedQuality Assurance
Soft Skills
LeadershipCommunicationInterpersonal Skills
Industry Keywords
Good Clinical Practice (GCP)Clinical Trial ManagementSite SatisfactionSite RetentionLife Sciences

About the role

Key responsibilities & impact
  • Oversee scientific operations workstreams, ensuring deliverables meet quality and timeline expectations
  • Manage site engagement efforts and maintain strong relationships and clear communication between clinical trial sites and ICON teams
  • Lead and mentor a team of site engagement professionals through study initiation, conduct, and closeout
  • Collaborate with clinical operations and project management teams to align site engagement strategies with study goals
  • Identify and address site concerns and provide solutions to enhance site performance and trial success
  • Drive initiatives to improve site satisfaction and retention
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements

Requirements

What you’ll need
  • Bachelor's degree in life sciences, business management, or a related field
  • Significant experience in site engagement or clinical operations
  • Proven experience managing site relationships and engagement in a clinical trial setting
  • Strong knowledge of regulatory and operational requirements
  • Strong leadership and team management skills
  • Excellent communication and problem-solving abilities
  • Strong organizational and project management skills
  • Ability to manage multiple sites and maintain clear communication
  • Detail-oriented and proactive, with a commitment to maintaining high standards of site satisfaction and regulatory compliance
  • 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