Remote Senior Clinical Trial Manager: Global Lead

ICON Clinical Research

México

Remote

MXN 900,000 - 1,500,000

Full time

10 days ago
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Job summary

ICON plc is seeking a Senior Clinical Trial Manager to oversee planning, execution and delivery of complex trials across US sites, with involvement in Mexico, Brazil, Colombia, Peru and Chile. The role focuses on study start-up, enrollment, budget oversight and cross-functional leadership.

The successful candidate will manage global trial components, mentor CRAs, and travel ~25% to ensure trial integrity and timelines while collaborating with Sponsors and vendors in a diverse, inclusive

Qualifications

  • Minimum 4+ years in a Clinical Trial Management role at a CRO or pharmaceutical company.
  • Bachelor's degree in health, life sciences, or related field.
  • At least 10+ years of relevant experience in clinical trial management.
  • Preferred: 2+ years of monitoring experience.
  • Experience with complex protocols (e.g., MASH/NASH, radiopharmaceuticals) and global trials.
  • Willingness to travel ~25%.

Responsibilities

  • Coordinate clinical trial management delivery and issue resolution.
  • Oversee budget portion of clinical trials for efficient resource allocation.
  • Develop monitoring plans and tools for effective study oversight.
  • Train and mentor CRAs to optimize performance.
  • Lead study start-up and enrollment, adhering to timelines.
  • Foster relationships with sponsors, vendors and cross-functional teams.

Skills

CTM leadership
Budget management
Study start-up
Team mentoring
Travel readiness

Education

Bachelor's degree in health or life sciences

Job description

ICON plc is seeking a Senior Clinical Trial Manager to oversee planning, execution and delivery of complex trials across US sites, with involvement in Mexico, Brazil, Colombia, Peru and Chile. The role focuses on study start-up, enrollment, budget oversight and cross-functional leadership.

The successful candidate will manage global trial components, mentor CRAs, and travel ~25% to ensure trial integrity and timelines while collaborating with Sponsors and vendors in a diverse, inclusive

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