Senior Clinical Research Associate

Reposted 19 Hours Ago
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6 Locations
In-Office or Remote
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.
Summary Generated by Built In
Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


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.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • 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

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Skills Required

  • Bachelor's degree in Life Science, Physical Science, Nursing or Biological Science
  • 3 years of monitoring experience
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines
  • Strong problem-solving skills
  • Exceptional verbal and written communication skills
  • Ability to manage multiple priorities in a dynamic environment
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The Company
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