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ICON plc
ICON plc
ConsultingHealthcareLogistics
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
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Senior Clinical Trial Manager - Mexico Remote

Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.

BRBrazilCLChileCOColombiaMXMexicoPEPeruRemoteFull-timeSeniorEnglish RequiredClinical Research

Description

  • Lead the planning, execution, and completion of clinical trials
  • Maintain compliance with study timelines, budgets, and regulatory requirements
  • Coordinate clinical trial delivery, resolve operational issues, and strengthen team capabilities
  • Manage the clinical budget and allocate resources efficiently
  • Create monitoring plans and tools to support effective study oversight
  • Train and mentor Clinical Research Associates (CRAs)
  • Drive participant enrollment and lead study start-up activities
  • Review trip reports and introduce corrective and preventive action plans when needed
  • Build effective working relationships with sponsors, vendors, and cross-functional teams
  • Provide strategic direction to support successful clinical trial outcomes

Requirements

  • At least 4 years of Clinical Trial Management experience within a CRO or pharmaceutical organization
  • A bachelor's degree in health sciences, life sciences, or a related field
  • At least 10 years of relevant clinical trial management experience
  • Monitoring experience of 2 or more years is preferred
  • Experience supporting complex protocols, such as MASH/NASH, radiopharmaceutical, or other specialized therapeutic programs, is highly valued
  • Experience managing complex or global clinical trials is advantageous
  • Experience overseeing all trial components from start-up through database lock is preferred
  • This position is for experienced CTM professionals; entry-level CTM experience alone is insufficient
  • Willingness to travel approximately 25% as required
  • Legal authorization to work in the country where the role is based

Benefits

  • Competitive base salary with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career pathways supporting learning and development

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