Coordinate clinical research activities in Kimberley through accurate documentation and site communication. Support Phase III trial operations within a global Contract Research Organization.
This entry-to-mid-level Clinical Trial Assistant role helps clinical research teams maintain organized study operations. You will coordinate meetings, travel, supplies, and essential documents while supporting recruitment tracking. The position also requires attention to Positive Clinical Practice, ICH guidelines, and regulatory requirements.
Key Responsibilities: Coordinate study meetings, travel arrangements, and information distribution
Collect, review, and track essential clinical site documents
Help manage supplies and equipment delivered to sites




Track patient recruitment and retention activities
Liaise with investigators and site staff as directed
Requirements: Previous clinical trial or healthcare administrative experience
Strong attention to detail, accuracy, and time management
Excellent written and verbal communication skills
Proficiency in Word, Excel, Outlook, and PowerPoint
Ability to work independently and within a team
Apply organizational, communication, and coordination strengths while supporting investigators, sites, and Phase III clinical research.

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📌 Clinical Research Trial Coordinator (British Columbia)
🏢 Placements24
📍 British Columbia