ICON plc

Senior Clinical Research Associate

ICON plc$95K — $115K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3+ years of monitoring experience in clinical trials.
  • Bachelor's degree in Life Science, Physical Science, Nursing, or Biological Science is required.
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.
  • Experience with risk mitigation and problem-solving at clinical trial sites.
  • Strong interpersonal and communication skills tailored for diverse stakeholders.
  • Ability to manage multiple priorities independently in a fast-paced environment.
  • Located in the Central/West Region of the US with regional travel capability.

Responsibilities

  • Support a single study focusing on cardiovascular/electrophysiology devices, specifically A-fib.
  • Monitor and ensure compliance with study protocols and regulatory requirements.
  • Establish and maintain effective relationships with site personnel and investigators.
  • Identify issues at study sites and implement effective solutions promptly.
  • Develop and execute communication plans tailored for study teams and sites.
  • Provide detailed reports about trial progression and compliance.
  • Manage regional travel for site visits, covering up to 65% of the time.

Benefits

  • Various annual leave entitlements.
  • A range of health insurance offerings for employees and families.
  • Competitive retirement planning options.
  • 24-hour access to a Global Employee Assistance Programme for well-being support.
  • Life assurance coverage provided.
  • Flexible, country-specific optional benefits such as childcare vouchers and gym memberships.
Full Job Description
Senior Clinical Research Associate - Cardiovascular Device - Central/West Region

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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

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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