Clinical Trial Coordinator

About this role

Overview of the role will be to provide administrative support to assigned clinical trials as directed by the Local Clinical Monitor.

Key Activities:

• Collect, review and log study documents from investigator site personnel in preparation of study start-up. Organize and attend investigator meetings.
• Set-up, enter, update and monitor investigator site information in CTMS including names, addresses, contact numbers, recruitment numbers, completion dates, etc.
• Prepare correspondence between Local Clinical Monitor and investigator as directed by CML.

About you

• Advanced administrative skills attained through post-secondary education combined with3 years business experience at a senior/administrative level.
• Exceptional organizational, interpersonal (both internal and external) written and oral communication and negotiating skills combined with excellent time/project management skills.
• Advanced knowledge of PC software, including MS Word, MS Excel and MS PowerPoint.
• Practical experience in a clinical research environment is an asset.
• Able to work in a team-oriented environment.
• High degree of confidentiality and attention to detail is required.

What we offer

What We Offer

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