NextRaiseNextRaiseFind jobs
Sign inSign up free
Jobs / Clinical Research Associate in Canada
1 month ago
Apply with autofill
Apply with autofill
Icon·1 month ago
1 month ago

Clinical Research Associate

CanadaEntry · 0-2 yearsClinical Research Associate

Sign up free to see how well your resume matches this role.

Boost your chances at icon

How you compare FREE

?
Your scoreYour score: not yet known
→
62
Top 10%Top 10%: 62 out of 100

Top 10% of NextRaise users matched against Clinical Research Associate roles in Canada.

Must-have skills for this role

  • clinical research
  • monitoring
  • good clinical practice
  • gcp

PDF or DOCX · no account needed

Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

About this role

Clinical Research Associate - Canada - Multi-TA or Oncology

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.


We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

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.


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

Company

Icon
Canada

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Icon's careers site·first seen 25 Aug 2026·last verified 8 Sept 2026·How we source jobs

Similar jobs

  • Experienced Clinical Research Associate (CRA II/Sr CRA) - Montreal, QC Canada - Bilingual at thermofisherRemote, Canada–match not yet calculated
  • Clinical Trial Associate at iconBurlington, Canada–match not yet calculated
  • Experienced Clinical Research Associate (CRA II/Sr CRA) - Montreal, QC Canada - Bilingual at Thermo Fisher ScientificAlberta, Canada–match not yet calculated
  • Senior Clinical Trial Associate at iconBurlington, Canada–match not yet calculated
  • Clinical Trial Associate 1 or 2 at Xenon PharmaceuticalsVancouver, Canada–match not yet calculated

Browse more jobs

  • Clinical Research Associate jobs in Canada
  • Regulatory Affairs Specialist jobs in Canada
  • Clinical Data Manager jobs in Canada
  • Medical Writer jobs in Canada
  • Clinical Research Associate jobs in United States
  • Clinical Research Associate jobs in Germany