Clinical Research Associate II

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

📋 Description

• Conduct and document various onsite monitoring visits.

• Participate in study initiation processes (if applicable).

• Execute CRF reviews, source document verification, and query resolution.

• Manage communication and oversight of site activities.

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

• Coordinate with internal project teams regarding the progress of studies.

• Engage in feasibility assessments.

• Assist the regulatory team in preparing documentation for study submissions.

⛳️ Requirements

• Bachelor's degree in Life Sciences or a comparable combination of education, training, and experience.

• Proven independent on-site monitoring experience in North America.

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

• Proficient in both English and French.

• Competent in MS Office applications.

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

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

• Willingness to travel as needed.

• Valid driver's license required.

🏝️ Benefits

• Employees have the option to work remotely.

• Opportunities for skill enhancement.

• Chance to broaden therapeutic area experience.

• Potential to gain expertise in clinical research.