P

PSI CRO

Global CRO delivering on-time patient enrollment

Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCalgary, AB, CanadaNo salary listed

About the Job

Requirements

  • A College/University degree in Life Sciences or an equivalent combination of education, training, and experience.
  • Be located in Canada (West Coast).
  • Have 5+ years of independent on-site monitoring experience.
  • Have experience with all types of monitoring visits in phases I–III.
  • Have experience independently monitoring Oncology clinical trials.
  • Have experience independently monitoring Gastroenterology (IBD) clinical trials.
  • Be proficient in Microsoft Office applications.
  • Be able to plan, multitask, and work in a dynamic team environment.
  • Have communication, collaboration, and problem-solving skills.
  • Be able to travel up to 75%.
  • Have a valid driver's license.

Responsibilities

  • Act as the main line of communication between the project team, sponsor, and site.
  • Build and maintain good relationships with site staff involved in study conduct.
  • Prepare, conduct, and report site selection, initiation, routine monitoring, and close-out visits.
  • Ensure that subject recruitment targets are timely defined, communicated, recorded, and met, and that project timelines are followed at site level.
  • Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations.
  • Perform source data verification and follow up on data queries at site level; review and manage study risks at site level.
  • Ensure proper handling, use, accountability, reconciliation, and return of Investigational Products and clinical study supplies at sites.
  • Review essential study documents and reconcile the Investigator Site File (ISF) and Trial Master File (TMF) at site level.
  • Ensure quality, data integrity, and compliance at site level.
  • Conduct site audit preparation visits and resolve site audit findings.
  • Participate in study site audits and client onsite visits, as required.
  • Ensure the flow of documents and study supplies between the project team, site, and the Central/Regional Laboratory, Central Reviewer, or Warehouse.
  • Conduct project-specific training of site investigators.
  • Support preparation of Investigator newsletters.
  • Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level.
  • Support preparation of draft regulatory and ethics committee submission packages.
  • Support collection of IP-RED packages at site/country level.
  • Facilitate review and reconciliation of the study TMF at country and site levels.

About the Company

PSI CRO

Global CRO delivering on-time patient enrollment

PSI CRO is a global contract research organization that handles clinical trials for multiple therapeutic areas, with a focus on enrolling patients on schedule and delivering studies on time. Its services span feasibility assessments, trial planning, site selection, patient recruitment, and multi-continent trial execution across 50+ countries, backed by medical doctor resources dedicated to accurate timeline predictions. Unlike many CROs, PSI emphasizes predictable enrollment and on-time project delivery, aiming for high client satisfaction and repeat business through a pragmatic, no-nonsense approach. The company’s goal is to be regarded as the best CRO in the world by both clients and employees, achieved through reliable timelines, strong execution, and low staff turnover.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Switzerland
Founded
1995

Recently Posted Jobs

Explore more opportunities at PSI CRO

See more jobs