ICON plc

Clinical Research Associate, Masked – Ophthalmology

ICON plc

full-time

Posted on:

Location Type: Remote

Location: Remote • 🇺🇸 United States

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Job Level

JuniorMid-Level

Tech Stack

Google Cloud Platform

About the role

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

  • Bachelor's degree in a scientific or healthcare-related field (highly preferred)
  • Minimum of 2 years of experience as a Clinical Research Associate (on site monitoring experience required)
  • On-site monitoring experience required
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
Benefits
  • Competitive salary
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
  • Well-being and work life balance opportunities for you and your family

Applicant Tracking System Keywords

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

Hard skills
clinical trial processesprotocol compliancedata integritydata reviewquery resolutionstudy documentation preparationclinical study reportsICH-GCP guidelineson-site monitoring
Soft skills
organizational skillscommunication skillsattention to detailindependent workcollaborative workability to work in fast-paced environment
Certifications
Bachelor's degree in scientific fieldBachelor's degree in healthcare-related field
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