JUMP TO CONTENT

Clinical Research Associate- Ontario

  1. Toronto
2025-119893
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

 

En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.


What you will be doing:

 

  • Conduct clinical trial site visits including evaluation, initiation, monitoring and close out
  • Oversee and report on the conduct of clinical trials at a site level including and on-line site visit reports and updates to electronic management systems
  • Proactive site management including:
    • Building and maintaining solid and professional relationships with site staff
    • Facilitating subject enrolment incorporating recruitment strategies and action plans at site level
    • Maintaining site audit/inspection readiness
    • Ensuring appropriate safety reporting and use of on-line safety reporting/reviewing systems such as Intralinks
    • Verification of electronic case report form data against written and electronic source documentation as per study schema/monitoring plan
    • Responding to site queries and escalating issues in accordance with processes and timelines
    • Conducting IP accountability and reconciliation
    • Facilitating implementation of new technologies and systems at clinical sites (Electronic Data Capture, eSAE reporting)
    • Maintenance of site study supplies

 

 Operational Excellence:

  • Contribute to sponsor goals
  • Promote operational and scientific excellence
  • Identify opportunities and best practices with local/regional partners that will contribute to the overall operational effectiveness.

 

Gestion des sites d’essais cliniques

  • Effectuer des visites de sites d’essais cliniques : incluant l’évaluation, l’initiation, la surveillance et la clôture.

  • Superviser et rendre compte de la conduite des essais cliniques : au niveau du site, y compris les rapports de visites en ligne et les mises à jour des systèmes de gestion électroniques.

  • Gestion proactive des sites, incluant :

    • Établir et maintenir des relations solides et professionnelles avec le personnel du site.

    • Faciliter l’enrôlement des sujets en intégrant des stratégies de recrutement et des plans d’action au niveau du site.

    • Maintenir la préparation à l’audit/inspection du site.

    • Assurer la déclaration appropriée des événements indésirables et l’utilisation des systèmes de déclaration/évaluation en ligne tels qu’Intralinks.

    • Vérifier les données des formulaires électroniques de rapport de cas (eCRF) par rapport à la documentation source écrite et électronique, conformément au schéma de l’étude/plan de surveillance.

    • Répondre aux questions du site et escalader les problèmes conformément aux processus et délais.

    • Effectuer la responsabilité et la réconciliation des produits de l’essai (IP).

    • Faciliter la mise en œuvre de nouvelles technologies et systèmes sur les sites cliniques (Collecte de données électronique, déclaration eSAE).

    • Maintenir les fournitures d’étude du site.

Excellence opérationnelle

  • Contribuer aux objectifs du promoteur.

  • Promouvoir l’excellence opérationnelle et scientifique.

  • Identifier les opportunités et les meilleures pratiques avec les partenaires locaux/régionaux qui contribueront à l’efficacité opérationnelle globale.


You are:

 

  • BA/BS/BSc in the sciences or nursing equivalent
  • A trained CRA with on-site monitoring experience
  • Comprehensive knowledge and understanding of ICH-GCP
  • Fluent oral (face to face and telephone) and written English language skills
  • Able and willing to travel up to 60% of the time or as per local requirements
  • Possession of a full driver’s license
  • Able and willing to work from a designated and appropriate home office as per local requirements
  • Willing to attend and contribute to team meetings including mandatory training (remote/off-site)
  • Competent computer skills including working knowledge of common software packages
  • Working knowledge of trial management databases and on-line systems
  • Able to attend a 1 week face to face in-house training course as part of on-boarding training
  • Able and willing to work on several protocols/therapy areas
  • Experience in phase II and phase III trials (preferred)
  • Working knowledge of Electronic Data Capture (preferred)

 Experience/working knowledge of the oncology disease area (preferred)

  • Experience of Centralized/Risk Based/Targeted monitoring (preferred)
  • Experience of working within a metric based environment (preferred)

 

  • Diplôme universitaire en sciences de la vie ou en soins infirmiers (équivalent d'un BA/BS/BSc).

  • Certification d'infirmier(ère) autorisé(e) (RN) ou qualification académique/ professionnelle équivalente.

  • Expérience préalable en surveillance clinique sur site, généralement de 1 à 2 ans.

  • Connaissance approfondie des Bonnes Pratiques Cliniques (BPC/ICH-GCP) et des réglementations locales.

  • Compétences en communication orale et écrite en anglais, avec une maîtrise des termes médicaux.

List #1

Day in the life

A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Read more
A picture of Yemi Moses
Progressing as a CRA with ICON

Teaser label

Our People

Content type

Blogs

Publish date

05/23/2023

Summary

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to excell

Teaser label

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Read more
A picture of Suzaita
Suzaita's story - an insight into working in Clinical Research

Teaser label

A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Read more
Suzaita Hipolito

by

Suzaita Hipolito

Suzaita Hipolito

by

Suzaita Hipolito

View all

Similar jobs at ICON

Clinical Research Associate (Chicago)

Salary

Location

United States

Department

Clinical Monitoring

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-119949

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Clinical Research Associate (Nebraska)

Salary

Location

United States

Department

Clinical Monitoring

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-119292

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Study Support Assistant (Vitória/ES)

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

2025-119862

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Contract Analyst II

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Contract Analyst II to join our diverse and dynamic team. As a Contract Analyst II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpre

Reference

2025-118786

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
CRA II

Salary

Location

Chile, Santiago

Department

Clinical Monitoring

Location

Santiago

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in desig

Reference

JR130554

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
CRA II and Senior CRA

Salary

Location

US, Portland, OR

Department

Clinical Monitoring

Location

Portland

Downers Grove

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli

Reference

JR128848

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above