Clinical Research Associate
@ ICON Strategic Solutions

Hybrid
CA$90,000
Hybrid
Full Time
Posted 20 hours ago

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XXXXXXXX XXXXXXXXXXX XXXXXXXX***** @iconplc.com
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Job Details

About ICON Strategic Solutions

ICON plc is a world-leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence. Join us on our mission to shape the future of clinical development.

Role Overview: Clinical Research Associate

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.

Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits.
  • Ensure protocol compliance, data integrity, and patient safety.
  • Collaborate with investigators and site staff for smooth study conduct.
  • Perform data review and resolve queries to maintain high-quality clinical data.
  • Prepare and review study documentation including protocols and study reports.

Your Profile

Bachelor's degree in a scientific or healthcare-related field. Minimum 12 months onsite monitoring experience as a Clinical Research Associate is required. You must have in-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines, with strong organizational and communication skills. Must work independently and collaboratively in a fast-paced environment and be willing to travel at least 50% of the time. Bilingual in French/English is essential.

What ICON Can Offer You

Along with a competitive salary, ICON offers diverse benefits including annual leave entitlements, comprehensive health insurance, competitive retirement planning, a global employee assistance program, life assurance, and flexible country-specific optional benefits. Visit our careers site to read more about the benefits ICON offers.

Commitment to Inclusion

At ICON, inclusion and belonging are fundamental to our culture and values. We provide an inclusive and accessible environment, free of any discrimination and harassment.

Application Note

If you require accommodations during the application process, please let us know. Even if you are unsure about meeting every requirement, we encourage you to apply.

Key skills/competency

  • Clinical Trials
  • Monitoring
  • Data Integrity
  • Protocol Compliance
  • Healthcare
  • Documentation
  • Regulations
  • Analytical Skills
  • Communication
  • Bilingual
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How to Get Hired at ICON Strategic Solutions

🎯 Tips for Getting Hired

  • Customize your resume: Tailor experiences to clinical research.
  • Emphasize skills: Highlight trial monitoring and compliance.
  • Prepare for interviews: Research ICON Strategic Solutions details.
  • Network strategically: Connect with current ICON employees.

📝 Interview Preparation Advice

Technical Preparation

Review ICH-GCP guidelines effectively.
Study clinical trial protocols thoroughly.
Practice data query resolution techniques.
Familiarize with regulatory compliance standards.

Behavioral Questions

Describe teamwork in trial monitoring.
Discuss handling unexpected trial issues.
Explain managing independent work efficiently.
Share communication examples with investigators.

Frequently Asked Questions