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ICON plc
ICON plc
Asistență medicalăConsultanțăLogistică
ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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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.

BRBraziliaCLChileCOColumbiaMXMexicPEPeruRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică

Descriere

  • 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

Cerințe

  • 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

Beneficii

  • 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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