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

Senior Clinical Trial Manager

ICON plc

. Coordinate clinical trial management delivery .

Posted 9/15/2026full-timeRemote • Pennsylvania • United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical trial management, including oversight of budgets, development of monitoring plans, and effective resource allocation. Proven ability to train and mentor Clinical Research Associates while fostering relationships with sponsors and cross-functional teams.

Highest-signal resume keywords
Clinical Trial ManagementBudget OversightTeam DevelopmentMonitoring ExperienceEnrollment Strategy

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
Clinical Trial ManagementMonitoring PlansResource AllocationCorrective Action PlansStudy Start-Up ActivitiesDatabase Lock ManagementComplex Trial ManagementTeam LeadershipTraining and MentoringIssue Resolution
Soft Skills
Relationship BuildingProblem SolvingCollaborationCommunicationLeadership
Industry Keywords
CROPharmaceuticalClinical ResearchHealth SciencesLife SciencesGlobal TrialsTrial ComponentsStudy OversightEnrollmentCross-Functional Teams

About the role

Key responsibilities & impact
  • Coordinate clinical trial management delivery
  • Resolve clinical trial issues
  • Develop team capability
  • Oversee the clinical portion of the budget to ensure efficient resource allocation
  • Develop monitoring plans and tools, ensuring effective study oversight
  • Train and mentor Clinical Research Associates (CRAs)
  • Drive enrollment and lead study start-up activities while adhering to timelines
  • Review trip reports and implement corrective and preventative action plans when necessary
  • Foster productive relationships with Sponsors, vendors, and cross-functional teams

Requirements

What you’ll need
  • A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization
  • Bachelor's degree in health, life sciences, or other relevant fields of study
  • At least 10+ years of relevant experience in clinical trial management
  • Preferred: 2+ years of monitoring experience
  • Experience in managing complex or global trials is advantageous
  • Preferred: Experience in managing all trial components from start-up to database lock
  • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives
  • Willingness to travel as required (approximately 25%)
  • 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