Senior Clinical Trial Manager

ICON plc

. Oversee the planning, execution, and successful completion of clinical trials .

Posted 10/2/2026full-timeRemote • Mexico, Chile, Colombia, Brazil, PeruSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in Clinical Trial Management, including oversight of trial planning, execution, and adherence to regulatory guidelines. Proven ability to mentor teams, manage complex protocols, and foster relationships with stakeholders to drive successful clinical outcomes.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceTeam MentoringComplex Protocol ManagementBudget Oversight

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial PlanningStudy Start-Up ActivitiesMonitoring Plan DevelopmentResource AllocationEnrollment StrategiesCorrective Action ImplementationDatabase Lock ManagementProtocol SupportTrial Component ManagementExperience with MASH/NASH

Soft Skills

Problem SolvingRelationship BuildingLeadershipCommunicationTeam Coordination

Industry Keywords

CROPharmaceuticalClinical Research AssociateGlobal TrialsTherapeutic Programs

About the role

Key responsibilities & impact

Oversee the planning, execution, and successful completion of clinical trials
Ensure adherence to timelines, budgets, and regulatory guidelines
Coordinate clinical trial management delivery, resolve issues, and develop team capability
Oversee the clinical portion of the budget and ensure efficient resource allocation
Develop monitoring plans and tools to ensure effective study oversight
Train and mentor Clinical Research Associates (CRAs)
Drive enrollment and lead study start-up activities
Review trip reports and implement corrective and preventative action plans when necessary
Foster productive relationships with Sponsors, vendors, and cross-functional teams
Provide strategic guidance to drive successful clinical trial outcomes

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 supporting complex protocols, including areas such as MASH/NASH, Radiopharmaceutical, or other specialized therapeutic programs, is highly valued
Experience in managing complex or global trials is advantageous
Preferred: Experience in managing all trial components from start-up to database lock
This role is intended for experienced CTM professionals; entry-level CTM experience alone will not meet the requirements
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