Study Assistant Professional

7 days ago

Ottawa, Ontario, Canada GLOBALFORCE-US Full time
Job Description

As a Clinical Trial Assistant at Globalforce-us, you will play a critical role in supporting our clinical research team. Your primary responsibilities will include:

- Study Support: Preparing and organizing study documentation, including protocols, informed consent forms, and case report forms (CRFs).
- Participant Management: Assisting with participant recruitment efforts, scheduling visits, and maintaining communication with study participants throughout the trial.
- Data Management: Collecting and processing study specimens, completing data entry for studies, and verifying clinical trial data to ensure accuracy and compliance with Good Clinical Practice (GCP) guidelines.
- Regulatory Compliance: Maintaining regulatory documents and files, ensuring all study materials are up-to-date and compliant with GCP guidelines.
- Meeting Coordination: Scheduling and coordinating study meetings, preparing agendas, and taking meeting minutes to facilitate effective communication within the team.
- Inventory Management: Tracking and managing study supplies and equipment, ensuring availability for study activities.

Requirements

- Bachelor's degree or equivalent training required via work experience or education.
- At least one year of previous job-related experience preferred.
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively.
- Excellent communication and interpersonal skills, with a focus on teamwork and collaboration.
- Basic understanding of clinical trial processes and regulatory requirements is preferred.
- Proficient in Microsoft Office Suite and familiarity with clinical trial management systems (CTMS) is a plus.

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