Apply

Ready to go for it?

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

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

See all jobs on JobTailor

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

Clinical Trial Manager

ICON plc

Clinical Trial Manager at ICON overseeing clinical trial operations to ensure quality outcomes. Collaborating with teams and stakeholders to adhere to timelines and guidelines.

Posted 7/18/2026full-timeRemote • 🇦🇷 ArgentinaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical trial management, ensuring compliance with regulations and quality standards while effectively collaborating with cross-functional teams and stakeholders. Possesses strong problem-solving skills and the ability to drive clinical deliverables in a designated therapeutic area.

Highest-signal resume keywords
Clinical Trial ManagementRegulatory ComplianceCross-Functional CollaborationProblem-SolvingMonitoring Experience

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 ProtocolsTrial DesignVendor SelectionRisk ManagementBudget Management
Soft Skills
Relationship ManagementDecision-Making
Industry Keywords
Clinical TrialsTherapeutic Area ExpertiseEthical GuidelinesLocal RegulationsNational RegulationsInternational Regulations

About the role

Key responsibilities & impact
  • Manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes
  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures
  • Build and manage strong relationships with trial investigators and stakeholders
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management

Requirements

What you’ll need
  • University degree in medicine, science, or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience
  • Advanced level of English

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