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ICON plc

Senior Clinical Trial Manager

ICON plc

. Oversee the clinical portion of the budget to ensure efficient resource allocation.

Posted 9/18/2026full-timeSao Paulo • BrazilSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Clinical Trial Management, including oversight of clinical budgets, monitoring plans, and study start-up activities. Proven ability to mentor Clinical Research Associates and manage complex trials across various therapeutic areas.

Highest-signal resume keywords
Clinical Trial ManagementCRA MonitoringTeam LeadershipRisk MitigationBudget Oversight

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial ManagementCRA MonitoringBudget ManagementStudy Start-UpData ManagementRisk AssessmentCorrective Action PlanningTherapeutic Area ExpertiseEnrollment StrategiesPerformance Optimization
Soft Skills
MentoringRelationship BuildingCommunicationCollaborationProblem Solving
Industry Keywords
CROPharmaceuticalCardiovascularDiabetesObesityImmunologyDermatologyGIRespiratoryGlobal Trials

About the role

Key responsibilities & impact
  • 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) to optimize their performance.
  • Drive enrollment and lead study start-up activities, 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.
  • Identify and mitigate risks.
  • Provide comprehensive reporting on all clinical activities.

Requirements

What you’ll need
  • MUST have previous experience in a Clinical Trial Management position (CTM) at a CRO or Pharmaceutical Organization.
  • Bachelor's degree in health, life sciences, or other relevant fields of study.
  • Strong previous relevant experience in clinical trial management CRA monitoring.
  • Strong previous experience years of monitoring experience.
  • Experience in managing complex or global trials is advantageous.
  • Experience working in therapeutic areas such as Cardiovascular, Diabetes, and Obesity as a priority; Immunology, Dermatology, GI, and Respiratory will also be considered.
  • Experience in managing all trial components from start-up to database lock is preferred.
  • Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives is preferred.
  • Fluency in English (reading, writing, speaking).
  • 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