ICON plc Logo

ICON plc

Clinical Research Associate

Posted 26 Days Ago
Be an Early Applicant
Remote
Hiring Remotely in Canada
Junior
Remote
Hiring Remotely in Canada
Junior
As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.
The summary above was generated by AI
Clinical Research Associate - Vancouver, Canada

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 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

6 Days Ago
Remote
2 Locations
Mid level
Mid level
Biotech
Manage site relationships and monitor clinical trials to ensure participant safety and data integrity per ICH GCP, regulatory requirements, and sponsor/SOPs. Conduct site selection, initiation, monitoring, and close-out visits (onsite or remote), support regulatory submissions and TMF/CTMS maintenance, drive recruitment, report study progress, escalate issues, and assist project managers to ensure timely study execution.
7 Days Ago
Remote
Québec, QC, CAN
Senior level
Senior level
Pharmaceutical
Lead site selection, initiation, monitoring (onsite and remote), and close-out activities for oncology clinical trials. Ensure ICH‑GCP, local regulations, and sponsor SOP compliance; manage regulatory submissions, drug accountability, data quality, safety reporting, eTMF/CTMS updates, and readiness for audits/inspections while supporting site performance and risk‑based monitoring.
Top Skills: CtmsEtmfRemote Monitoring
13 Days Ago
Remote
CAN
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical
Perform site qualification, initiation, monitoring (on-site or remote) and close-out to ensure ICH-GCP/GPP and protocol compliance. Verify informed consent, source documents, CRF data, IP handling, ISF/TMF reconciliation, and query resolution. Document activities, support recruitment/retention, prepare for audits, train/mentor junior CRAs, and manage site communications and timelines. May support Real-World Late Phase tasks including chart abstraction and country-level regulatory coordination.
Top Skills: Electronic Data Capture (Edc)Investigator Site File (Isf)Trial Master File (Tmf)

What you need to know about the Ottawa Tech Scene

The capital city of Canada and the nation's fourth-largest urban area, Ottawa has proven a rapidly growing global tech hub. With over 1,800 tech companies, many of which are leaders in their sectors, the city's tech talent now makes up more than 13 percent of its total workforce. This growth is driven not only by the big players like UL Solutions and Dropbox, but also by a thriving startup ecosystem, as new businesses emerge to follow in the footsteps of those that came before them.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account