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ICON plc

Site Management Associate II

ICON plc

. Support the management and monitoring of clinical trial sites .

Posted 11/11/2026full-timeRemote • BrazilJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial sites while ensuring compliance with study protocols and GCP guidelines. Proficient in analyzing site performance metrics and collaborating with cross-functional teams to maintain high-quality standards.

Highest-signal resume keywords
Clinical Research ExperienceSite ManagementGood Clinical Practice (GCP)Project Management SkillsAnalytical Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ProcessesRegulatory Document PreparationData AnalysisPerformance Metrics TrackingCompliance Monitoring
Soft Skills
Organizational SkillsCommunication SkillsInterpersonal SkillsMentoringAttention to Detail
Industry Keywords
Life SciencesHealthcare AdministrationClinical ResearchStudy ProtocolsCross-Functional Collaboration

About the role

Key responsibilities & impact
  • Support the management and monitoring of clinical trial sites
  • Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
  • Coordinate monitoring activities at clinical trial sites
  • Ensure adherence to study protocols and timely resolution of site-related issues
  • Assist in preparing and reviewing regulatory documents
  • Collaborate with cross-functional teams throughout the study lifecycle
  • Track site performance metrics, analyze data, and provide reports
  • Participate in training initiatives and mentor junior staff

Requirements

What you’ll need
  • Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
  • Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines
  • Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines
  • Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards
  • Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams
  • Willingness to travel as required (approximately 25%)
  • Legal right to work in Brazil

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