ICON plc Logo

ICON plc

Clinical Research Associate

Reposted 22 Days Ago
Be an Early Applicant
Remote
Hiring Remotely in United States of America
Junior
Remote
Hiring Remotely in United States of America
Junior
The Clinical Research Associate will conduct monitoring visits, ensure protocol compliance, collaborate with site staff, and maintain data integrity.
The summary above was generated by AI
Clinical Research Associate - Multi TA/Oncology - US

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.


Job Advert Posting

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • 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

  • Bachelor's degree in a scientific or healthcare-related field.

  • Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. 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.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.


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

Similar Jobs

3 Days Ago
In-Office or Remote
New Jersey, USA
111K-138K Annually
Senior level
111K-138K Annually
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead site-facing clinical monitoring for oncology studies: conduct selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety and drug accountability; support recruitment/retention; resolve data queries; escalate risks and coordinate with cross-functional clinical teams.
Top Skills: CtmsEtmf
3 Days Ago
In-Office or Remote
New Jersey, USA
91K-114K Annually
Junior
91K-114K Annually
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
Serve as the primary site contact for oncology trials, conduct site selection/initiation/monitoring/close-out visits, ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor safety reporting and drug accountability, support recruitment and data quality, escalate risks, and collaborate with cross-functional clinical teams.
Top Skills: CtmsEtmf
3 Days Ago
In-Office or Remote
Arizona, USA
Junior
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
Serve as primary sponsor contact for oncology clinical sites: perform selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety reporting and drug accountability; support recruitment, data quality, budgets, and cross-functional communication.
Top Skills: CtmsEtmf

What you need to know about the Charlotte Tech Scene

Ranked among the hottest tech cities in 2024 by CompTIA, Charlotte is quickly cementing its place as a major U.S. tech hub. Home to more than 90,000 tech workers, the city’s ecosystem is primed for continued growth, fueled by billions in annual funding from heavyweights like Microsoft and RevTech Labs, which has created thousands of fintech jobs and made the city a go-to for tech pros looking for their next big opportunity.

Key Facts About Charlotte Tech

  • Number of Tech Workers: 90,859; 6.5% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Lowe’s, Bank of America, TIAA, Microsoft, Honeywell
  • Key Industries: Fintech, artificial intelligence, cybersecurity, cloud computing, e-commerce
  • Funding Landscape: $3.1 billion in venture capital funding in 2024 (CED)
  • Notable Investors: Microsoft, Google, Falfurrias Management Partners, RevTech Labs Foundation
  • Research Centers and Universities: University of North Carolina at Charlotte, Northeastern University, North Carolina Research Campus

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account