ICON plc Logo

ICON plc

Clinical Research Associate

Posted 18 Days Ago
Be an Early Applicant
In-Office or Remote
6 Locations
91K-114K Annually
Junior
In-Office or Remote
6 Locations
91K-114K Annually
Junior
Conduct clinical trial monitoring for early-stage oncology studies, including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support clinical study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring expertise, a scientific or healthcare degree, and willingness to travel up to 50% within the assigned region.
The summary above was generated by AI
Clinical Research Associate - Women's Oncology - West / Central / South Region

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


What You Will Do:


You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:


You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • Oncology monitoring experience required
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required up to 50% within their region (West, Central or South)

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.


Salary Range

$91,336.00-$114,170.00

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

ICON plc Chicago, Illinois, USA Office

525 W Monroe St Ste 1000, Chicago, Illinois, 60661-3791, United States, Chicago, United States, 60661-3791

Similar Jobs

Yesterday
Remote
10 Locations
111K-138K Annually
Senior level
111K-138K Annually
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct site management and monitoring for oncology clinical trials, including qualification, initiation, interim, and close-out visits. Ensure data integrity, subject safety, inspection readiness, regulatory compliance, and essential document reconciliation. Manage site relationships, feasibility, activation, IRB/EC submissions, risk indicators, and CAPA plans. Train site staff on protocols, GCP, SOPs, and regulations, while supporting inspections and mentoring junior CRAs. The role requires solid tumor oncology trial expertise and travel up to 50%.
Top Skills: Corrective Action And Preventive Action (Capa)Good Clinical Practice (Gcp)Good Practice (Gxp)Risk-Based MonitoringTrial Master File (Tmf)Veeva Systems
4 Days Ago
Remote
United States
Senior level
Senior level
Pharmaceutical
Monitors and manages clinical trial sites from qualification through closeout, ensuring protocol, GCP, regulatory, data, safety, documentation, and investigational product compliance. Conducts site visits, trains investigators, reviews source data and essential documents, tracks action items, maintains CTMS records, supports audits and study teams, and collaborates with sites and functional groups. Requires substantial travel and Phase I monitoring experience.
Top Skills: Clinical Trial Management System (Ctms)Electronic Data Capture (Edc)Electronic Trial Master File (Etmf)Ich/GcpExcelMicrosoft PowerpointMicrosoft SharepointMicrosoft Word
5 Days Ago
In-Office or Remote
6 Locations
91K-114K Annually
Junior
91K-114K Annually
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct clinical trial site qualification, initiation, monitoring, and close-out visits for oncology studies. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support preparation and review of study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring experience, scientific or healthcare education, ICH-GCP knowledge, and willingness to travel 60–75% within the region.
Top Skills: Clinical Trial MonitoringIch-Gcp

What you need to know about the Chicago Tech Scene

With vibrant neighborhoods, great food and more affordable housing than either coast, Chicago might be the most liveable major tech hub. It is the birthplace of modern commodities and futures trading, a national hub for logistics and commerce, and home to the American Medical Association and the American Bar Association. This diverse blend of industry influences has helped Chicago emerge as a major player in verticals like fintech, biotechnology, legal tech, e-commerce and logistics technology. It’s also a major hiring center for tech companies on both coasts.

Key Facts About Chicago Tech

  • Number of Tech Workers: 245,800; 5.2% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: McDonald’s, John Deere, Boeing, Morningstar
  • Key Industries: Artificial intelligence, biotechnology, fintech, software, logistics technology
  • Funding Landscape: $2.5 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Pritzker Group Venture Capital, Arch Venture Partners, MATH Venture Partners, Jump Capital, Hyde Park Venture Partners
  • Research Centers and Universities: Northwestern University, University of Chicago, University of Illinois Urbana-Champaign, Illinois Institute of Technology, Argonne National Laboratory, Fermi National Accelerator Laboratory

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account