Posted last month
Senior Clinical Research Associate
@ PSI CRO
Vancouver, British Columbia
Overview
PSI CRO is hiring a Senior Clinical Research Associate for full-time work monitoring clinical studies across several therapeutic areas. The role involves onsite monitoring visits, source document verification, site management and audit preparation. The posting requires independent on-site monitoring experience, a life sciences degree or equivalent, full working proficiency in English and French, and the ability to travel.
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
- 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 on-site monitoring experience in Phase II and/or III
- Oncology experience an asset
- Full working proficiency in English and French
- Valid driver's licence and ability to travel
Tools & skills
Source and dates
Employer career site / ATS feed · smartrecruiters
- Employer posting date
- 2026-09-28
- First seen by our source
- 2026-10-08
- Source record updated
- 2026-10-09
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Allied health |
| Hours per week | 40 (estimated) |
| Travel | ground: moderate |
| Work setting | Client sites, Office |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English, French |
| Driver’s licence | required |
| Education | Bachelor’s degree (required) |
| Fields of study | Life Sciences |
Summary and details written by AI from the posting; the employer’s posting is the authority.
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.
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…
| Field | Value |
|---|---|
| Industry | Pharmaceutical Manufacturing |
| Company size | 1,001-5,000 employees |
| Headquarters | Zug |
| Organization type | Privately Held |
| Specialties | Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3 |
| Open jobs on Jobsy | 7 |
| View page |
Company Description
PSI is a leading Contract Research Organization with 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 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 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 and French is essential.
- 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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