ICON plc

Senior Clinical Research Associate

ICON plc$110K — $138K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate with knowledge of clinical trial processes.
  • Ability to manage multiple sites and projects with strong organizational skills.
  • Expertise in monitoring practices, data integrity, and site management.
  • Excellent communication and stakeholder management skills essential for compliance.
  • Oncology monitoring experience is required.
  • Willingness to travel at least 60% of the time and possess a valid driver's license.

Responsibilities

  • Monitor clinical trial sites for adherence to study protocols and regulatory requirements.
  • Conduct site visits to resolve issues and support trial execution.
  • Collaborate with cross-functional teams for accurate data collection.
  • Provide training and guidance to site staff and CRAs for high standards.
  • Build and maintain relationships with site personnel and stakeholders.

Benefits

  • Various annual leave entitlements.
  • Range of health insurance offerings for you and your family.
  • Competitive retirement planning opportunities.
  • Global Employee Assistance Programme for 24-hour support.
  • Life assurance.
  • Flexible country-specific optional benefits such as childcare vouchers and gym memberships.
Full Job Description
Senior CRA - Colorado - Oncology

What You Will Be Doing:
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Must be located in the Colorado
  • Oncology monitoring experience is required
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license


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.

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

Similar Jobs

More Jobs at ICON plc

More Pharmaceuticals & Biotech Jobs

Find similar Senior Clinical Research Associate jobs: