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Senior Clinical Research Associate

United States, Kansas City · Job Posted June 01, 2026
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Job Description

Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions. ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib. The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered. 3 years of monitoring experience required. A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science. Candidates must have/ be: In-depth knowledge of FDA regulations and ICH/GCP guidelines. Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly. Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams. Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely. Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment. Ability to work independently and manage multiple priorities in a dynamic environment. A well-executed plan for communication with the study teams and sites. Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports. Located in the US near a major airport. Ability to cover up to 65% regional travel.

Job Responsibility

support 1 study in the cardiovascular/electrophysiology medical device space

Requirements

  • 3 years of monitoring experience required
  • A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment
  • Ability to work independently and manage multiple priorities in a dynamic environment
  • A well-executed plan for communication with the study teams and sites
  • Well-versed in clinical trial management
  • Located in the US near a major airport
  • Ability to cover up to 65% regional travel

Nice to have

  • cardiovascular medical device monitoring experience
  • cardiovascular/electrophysiology pharma monitoring experience

What we offer

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others
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