ICON plc
ICON plc
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.

Clinical Trial Manager II at ICON plc – Remote in Argentina

Lead clinical trial operations, data review, and regulatory compliance for ICON plc, a global clinical research organization. Coordinate cross-functional teams and study deliverables in a remote role based in Buenos Aires.

Description

  • Manage clinical trial workstreams and ensure deliverables meet quality and timeline requirements
  • Partner with cross-functional teams to plan and execute effective participant enrollment strategies
  • Create and implement comprehensive clinical trial protocols with relevant internal teams
  • Direct daily clinical trial operations in accordance with applicable regulatory standards
  • Review and interpret trial data, identify trends, and recommend ways to improve study outcomes
  • Anticipate execution challenges and implement practical solutions to keep trials on track
  • Build effective relationships with internal and external stakeholders to support smooth trial delivery
  • Balance competing priorities while supporting team development

Requirements

  • Bachelor's degree in a relevant field
  • At least [X] years of experience managing clinical trials
  • Demonstrated expertise in clinical trial design and execution
  • Strong knowledge of applicable regulatory requirements
  • Advanced analytical and problem-solving abilities
  • Ability to interpret complex medical data
  • Clear and effective communication and interpersonal skills
  • Ability to work collaboratively across diverse teams
  • Strong attention to detail and organizational skills
  • Proven ability to manage multiple tasks and competing priorities successfully
  • Willingness to travel as needed, approximately 25%
  • Legal authorization to work in the country where the role is based

Benefits

  • Competitive base pay 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 development opportunities