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Posted 15 days ago

Senior Clinical Research Associate

@ PSI CRO

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Toronto, Ontario

$120k–$150k/yrRemoteFull-time
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SIGNALS

Overview

PSI CRO is hiring a freelance Senior Clinical Research Associate in Canada to conduct onsite monitoring visits and manage study sites for clinical trials. The role requires independent monitoring experience in Phase II and/or III studies, with travel and a valid driver's licence. PSI states it does not sponsor work visas.

Pay:

$120,000–$150,000 a year

Responsibilities:

  • Conduct SIV, RMV and COV onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Manage site communication and act as point of contact for vendors
  • Support regulatory team with study submission documents
  • Prepare for and participate in audits and inspections

Requirements summary:

  • College or university degree in life sciences or equivalent
  • Independent onsite monitoring experience
  • Experience in all monitoring visit types in Phase II and/or III
  • Full working English proficiency
  • Valid driver's licence and ability to travel

Tools & skills

MS Office
Source and dates

Employer career site / ATS feed · smartrecruiters

Employer posting date
2026-10-23
First seen by our source
2026-10-23
Source record updated
2026-10-23

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SenioritySenior
DepartmentAllied health
Hours per week40 (estimated)
Travelground: moderate
Work settingClient sites, Office
PositionSitting and standing
Physical demandsphysical low · computer high
LanguagesEnglish
Driver’s licencerequired
EducationBachelor’s degree (required)
Fields of studyLife Sciences

Summary and details written by AI from the posting; the employer’s posting is the authority.

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PSI CRO

Saved company profile

Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.

Full company description

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 effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

LinkedIn followers
329,384
People associated on LinkedIn
2,861
Reported office locations
  • Baarerstrasse 113a, Zug, 6300, CH
Business categories
  • Business Information Systems
  • Health Care
  • Pharmaceutical
Other recorded names
  • PSI CRO
Specialties
  • Number One Patient Enrollment CRO
  • Clinical Research
  • Clinical Trials
  • Oncology
  • Hematology
  • Multiple Sclerosis
  • Infectious Diseases
  • Patient Enrollment
  • Phase 2
  • Phase 3
  • Pivotal Trials
  • Global Clinical Trials
  • Full-Service Clinical Trials
  • and Radiopharmaceuticals
Profile identifies a recruitment agency
No
Reported total investment
0

Currency and observation date were not supplied; this is not a current valuation or a funding round.

View all jobs Website

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 effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s…

FieldValue
IndustryPharmaceutical Manufacturing
Company size1,001-5,000 employees
HeadquartersZug
Organization typePrivately Held
SpecialtiesNumber One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3
Open jobs on Jobsy7
LinkedInView page
Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:

  • Conduct and report SIV, RMV, COV onsite monitoring visits
  • 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
  • Prepare and particiapte on audits and inspections

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
  • Experience in Oncology is a plus
  • Full working proficiency in English.
  • 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

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

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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