Senior Clinical Research Associate

PSI CRO

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profile Job Location:

Montreal - Canada

profile Monthly Salary: Not Disclosed
Posted on: 10 hours ago
Vacancies: 1 Vacancy

Job Summary

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects rights safety and well-being and quality of data compliance.

Home-based in Quebec Canada. 

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review source document verification and query resolution
  • Be responsible for site communication and management
  • Supervise study activities timelines and schedules on the country level
  • Be a point of contact for in-house support services and vendors
  • Be involved in quality control such as compliance monitoring and reports review
  • 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
  • Experience in all types of monitoring visits in Phase II and/or III
  • Participation in clinical projects as a Lead/Senior Monitor
  • Experience in Oncology
  • 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 drivers license (if applicable)

Additional Information :

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.


Remote Work :

Yes


Employment Type :

Full-time

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus ...
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Key Skills

  • CSS
  • Cloud Computing
  • Health Education
  • Actuary
  • Building Electrician

About Company

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PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effo ... View more

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