Clinical Research Associate II

PSI CRO · Remote · Canada, Brazil only

Canada, Brazil only25+ years requiredPublished 4 November 2026Check carefully

Apply on PSI CRO's site✨ Tailor my resume for this job🎤 Practise the interview question, free

✓ Straight from PSI CRO's own careers page. No middlemen, no “we'll send you a check for equipment”. How we check jobs

✓ Sent 100 applications and heard nothing? Make this one count: tailor your resume to this ad in one tap, free.

First recorded by Psst: 5 November 2026. Sign in with Google to continue to the employer. A free account is enough.

Free interview practice

Practise the first interview question for this job

If PSI CRO replies, the first call usually starts with a question like this. Vague answers are the easiest to reject. Write yours and get an AI score in under a minute.

The 20-second read

Experience
25+ years required
Where you can live
Canada, Brazil only
Languages
English, Spanish
Degree or licence
Mentioned (university degree)
Job type
Full-time

Read from the ad by Psst's rules. Check the full ad below before applying.

Job details

Where you can work
Canada, Brazil
Employment type
Full-time
Advertised pay
Not stated by the employer
Experience
25+ years required
Employer publication date
4 November 2026
First recorded by Psst
5 November 2026
Last checked at the source
8 November 2026

About the job

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 all types of onsite monitoring visits
  • Be involved in study startup and feasibility research
  • 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
  • Support regulatory team in preparing documents for study submissions
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience Argentina
  • Experience in all types of monitoring visits in Phase II / III
  • Experience in Oncology is preferred
  • Full working proficiency in English and Spanish
  • Proficiency in MS Office applications
  • Ability to plan and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

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

PSI is a leading Contract Research Organization with more than 25 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.

Apply on PSI CRO's site✨ Tailor my resume for this jobPrepare with the Apply kitMore remote clinical research jobs →

Find my remote job matches →
Ghost Job Detector: Check carefully
  • Reposted
  • No pay listed
Signals, not proof. Check the company's page before you spend time on it.
Free to build · no sign-up

A resume that gets past the first 6 seconds

Recruiters skim. The Psst resume coach fixes what makes them skip you, line by line, and one tap tailors it to the exact job you're applying to.

  • 1Every line checkedWeak starts, clichés and AI-sounding phrases flagged, with a 3-question fix.
  • 2Tailored to the jobSee which skills and tools from the ad your resume is missing. Try it free on one of your matches.
  • 3Ready for remoteTime zone, tools and proof you work on your own, the things remote teams look for.
  • 4Looks the partOne page, 6 designs, 8 colours and a matching cover letter, free to build. Premium downloads the PDF and Word files.
Try the resume coach →Compare Premium

Set up your job alert