Clinical Research Associate II in Toronto

Clinical Research Associate II in Toronto

Toronto Full-Time 98000 - 120000 $ / year (est.) On-site
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At a Glance

  • Tasks: Conduct onsite monitoring visits and manage communication for clinical studies.
  • Company: Join PSI, a leading Contract Research Organization with over 30 years of experience.
  • Benefits: Competitive salary, skill development, and a dynamic work environment.
  • Other info: Great opportunity for career growth and to work in diverse therapeutic areas.
  • Why this job: Make a real impact in clinical research while expanding your expertise.
  • Qualifications: Degree in Life Sciences and independent monitoring experience required.

The predicted salary is between 98000 - 120000 $ per year.

  • Compensation: CAD 98,000 - CAD 120,000 - yearly
  • Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.

We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup (if applicable)
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in North America.
  • Experience in all types of monitoring visits in Phase II and/or III
  • Full working proficiency in English and French.
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel
  • Valid driver’s license
  • Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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Clinical Research Associate II in Toronto employer: PSI CRO

At PSI, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. As a Clinical Project Management Lead, you will benefit from our commitment to employee development, competitive compensation, and the opportunity to make a meaningful impact in clinical research across North America. Join us in a dynamic environment where your leadership will drive success and contribute to advancements in healthcare.

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Contact Details:

PSI CRO Recruitment Team

We think you need these skills to ace Clinical Research Associate II in Toronto

Onsite Monitoring
Clinical Study Management
CRF Review
Source Document Verification
Query Resolution
Site Communication
Project Team Collaboration