Senior Clinical Research Associate

This is a fully remote position, open to applicants in Canada.

📋 Description

• Execute and document onsite monitoring visits for SIV, RMV, and COV.

• Conduct reviews of CRFs, verify source documents, and resolve queries.

• Oversee communication and management at the site.

• Serve as a liaison for in-house support services and vendors.

• Liaise with internal project teams about the progress of the study.

• Engage in feasibility assessments.

• Assist the regulatory team in the preparation of documents for study submissions.

• Prepare for and actively participate in audits and inspections.

⛳️ Requirements

• A college or university degree in Life Sciences or a comparable combination of education, training, and experience.

• Experience in independent onsite monitoring.

• Familiarity with all types of monitoring visits in Phase II and/or III.

• Experience in Oncology is advantageous.

• Full working proficiency in both English and French is mandatory.

• Skilled in the use of MS Office applications.

• Capable of planning, multitasking, and thriving in a dynamic team environment.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel.

• A valid driver’s license is required.

🏝️ Benefits

• Enhance your skill set.

• Expand your experience in various therapeutic areas.

• Achieve expertise in clinical research.