Clinical research associate
Job Details
British Columbia, British Columbia, Canada
Groom & Associés / Associates
Posted today
Want updates for this and similar Jobs?
Full Job Description
Job Title: Clinical Research Associate (CRA) – British Columbia Region
Location: Remote (British Columbia-based)Type: Contract (until October
30, 2028)Start Date: As soon as possible Compensation: Commensurate
with experience (hourly or fixed-price contract)About the Role Groom &
Associates is seeking a detail-oriented and experienced Clinical
Research Associate (CRA) to support a global sponsor’s ongoing
clinical trial through remote and occasional on-site monitoring
activities.
The successful candidate will be home-based in British Columbia and provide oversight for investigative sites in the region.
Key Responsibilities Conduct remote Site Initiation Visits (SIVs) in accordance with study SOPs and regulatory requirements Lead quarterly remote monitoring calls with each assigned site (approx.
3 contacts per year per site)Perform Close-Out Visits remotely as per study timelines When required by the project team, conduct on-site monitoring visits (travel within British Columbia)Ensure adherence to Good Clinical Practice (GCP), study protocols, and sponsor expectations Maintain complete, accurate, and timely monitoring documentation Serve as a liaison between sponsor and site staff, facilitating communication and issue resolution Qualifications Bachelor’s degree in life sciences, nursing, or a related field Minimum 3 years of CRA experience, preferably in multi-site or pharmaceutical-sponsored trials Strong knowledge of ICH-GCP, Health Canada and FDA regulations Excellent communication, time management, and interpersonal skills Comfortable working independently from a home office with occasional travel Why Join Us?Join a high-impact study with a global sponsor Work remotely with flexible scheduling and travel only when necessary
The successful candidate will be home-based in British Columbia and provide oversight for investigative sites in the region.
Key Responsibilities Conduct remote Site Initiation Visits (SIVs) in accordance with study SOPs and regulatory requirements Lead quarterly remote monitoring calls with each assigned site (approx.
3 contacts per year per site)Perform Close-Out Visits remotely as per study timelines When required by the project team, conduct on-site monitoring visits (travel within British Columbia)Ensure adherence to Good Clinical Practice (GCP), study protocols, and sponsor expectations Maintain complete, accurate, and timely monitoring documentation Serve as a liaison between sponsor and site staff, facilitating communication and issue resolution Qualifications Bachelor’s degree in life sciences, nursing, or a related field Minimum 3 years of CRA experience, preferably in multi-site or pharmaceutical-sponsored trials Strong knowledge of ICH-GCP, Health Canada and FDA regulations Excellent communication, time management, and interpersonal skills Comfortable working independently from a home office with occasional travel Why Join Us?Join a high-impact study with a global sponsor Work remotely with flexible scheduling and travel only when necessary
Show more
Report Job
Clinical Research Associate
Groom & Associés / Associates
All Direct Job Ads are subject to ClickaJobs Terms of Service. We allow users to flag postings that may be in violation of those terms. Job Ads may also be flagged by ClickaJobs. However, no moderation system is perfect, and flagging a posting does not ensure that it will be removed.
Report to ClickaJobs