Clinical Research Assistant Remote or On-site

Embark on a pivotal career as a Clinical Research Assistant with Everest in Toronto/Markham, Ontario. This dual work model allows you to operate on-site or remotely while supporting medical writing and safety monitoring projects.

As a Clinical Research Assistant, you will be instrumental in ensuring accurate documentation and regulatory compliance. With a focus on quality control and data verification, your expertise in clinical trials will be vital. A Bachelor’s degree in Clinical, Medical, or Life Sciences is required, along with understanding medical terminology and regulatory standards.

Key Responsibilities:

• Conduct QC reviews for medical documents

• Perform data verification against patient CRFs

• Learn document e-publishing for clinical trials

• Assist in archiving clinical trial documents

• Manage deliverables and timelines for projects

Requirements:

• Bachelor’s in Clinical or Life Sciences

• Experience in clinical trials in a pharmaceutical setting

• Strong communication and organizational skills

• Detail-oriented and quality-focused

• Proficiency in Microsoft Office applications

Elevate your career with Everest by ensuring regulatory compliance and quality in clinical research.
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