Clinical Research Associate II

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

📋 Description

• Execute and document various onsite monitoring visits.

• Participate in study initiation processes, if required.

• Conduct CRF assessments, verify source documents, and resolve queries.

• Oversee communication and management at the site level.

• Act as a liaison for internal support services and vendors.

• Update internal project teams on study advancements.

• Engage in feasibility studies.

• Assist the regulatory team in organizing documents for study submissions.

⛳️ Requirements

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

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

• Familiarity with all forms 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 environment.

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

• Willingness to travel.

• Possession of a valid driver’s license.

🏝️ Benefits

• Remote work is allowed.

• Chance to enhance skill sets.

• Opportunity to broaden therapeutic area expertise.

• Potential to become a specialist in clinical research.