Clinical Trials Associate
New
J
JobgetherClinical research
Based in CanadaFull-TimeJunior
Salary16.83 - 33.65 USD per year
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Job Details
- Languages
- Excellent written and verbal English communication skills; fluency in the language of the country where the candidate is based (for Canada, English or French as applicable to the location and role requirements).
- Experience
- At least one year of experience in a related administrative, clinical research, or project support role.
- Required Skills
- Project CoordinationMicrosoft ExcelMicrosoft OfficePowerPoint
Requirements
- Have a university degree or equivalent professional experience.
- Have at least one year of experience in a related administrative, clinical research, or project support role.
- Have excellent written and verbal English communication skills.
- Be fluent in the language of the country where you are based; for Canada, proficiency in English or French applies according to location and role requirements.
- Have strong organizational skills and the ability to manage multiple tasks simultaneously.
- Be able to exercise independent judgment and work with appropriate autonomy.
- Demonstrate excellent attention to detail and a consistent focus on accuracy and quality.
- Have strong problem-solving skills and the ability to prioritize competing responsibilities.
- Be proficient in Microsoft Office applications, particularly Outlook, Word, Excel, and PowerPoint.
- Be able to collaborate and communicate effectively with project team members.
Responsibilities
- Coordinate and track system access for clinical project team members, including Project Managers, Lead CRAs, and CRAs.
- Maintain project portals and check that the latest approved document revisions are available.
- Support the preparation, organization, and shipment of clinical trial documentation.
- Assist with preparing and maintaining Investigator Site Files (ISFs).
- Manage document version control and quality checks.
- Submit and maintain relevant documentation within the Trial Master File (TMF).
- Track and update project-related information, including site medical question-and-answer logs.
- Provide day-to-day administrative and project tracking support to clinical project teams.
- Monitor assigned tasks and follow up to help ensure activities are completed accurately and on time.
- Collaborate with project team members to support clinical trial delivery.
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