ICON plc

Senior Clinical Research Associate

ICON plc$110K — $138K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3 years of monitoring experience in clinical research.
  • Bachelor's degree in Life Science, Nursing, or Biological Science is required.
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.
  • Strong problem-solving skills for risk management at study sites.
  • Excellent interpersonal skills for effective relationship-building with site personnel and teams.
  • Exceptional communication skills to clearly convey complex information.
  • Ability to manage multiple priorities and work independently in a dynamic environment.

Responsibilities

  • Support clinical studies in the cardiovascular/electrophysiology medical device space.
  • Monitor study sites to ensure compliance with regulatory guidelines.
  • Communicate collaboratively with site personnel and internal teams.
  • Identify and mitigate risks, proposing effective solutions promptly.
  • Manage communication plans for efficient information flow with study teams and sites.
  • Maintain rigorous documentation and reporting standards throughout the trial.
  • Travel regionally to oversee study site activities, covering up to 65% of the time.

Benefits

  • Various annual leave entitlements.
  • Flexible health insurance options for you and your family.
  • Competitive retirement planning offerings.
  • Global Employee Assistance Programme for family support.
  • Life assurance coverage.
  • Flexible benefits such as childcare vouchers and discounted gym memberships.
Full Job Description
Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions

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, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing 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 West region in the US near a major airport. Ability to cover up to 65% regional travel.


What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:
  • 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.


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

Salary range: $110,520.00-$138,150.00

Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.

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

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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