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 CRF assessments, verify source documents, and resolve queries.

• Oversee communication and management at the site level.

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

• Inform internal project teams about the progress of the study.

• Engage in feasibility assessments.

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

• Organize and participate in audits and inspections.

⛳️ Requirements

• College or university degree in Life Sciences, or a comparable mix of education, training, and experience.

• Proven experience in independent onsite monitoring.

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

• Oncology experience is advantageous.

• Full professional proficiency in English.

• Competence in MS Office applications.

• Capability to plan, multitask, and thrive in a dynamic team environment.

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

• Willingness to travel.

• Possession of a valid driver’s license.

🏝️ Benefits

• Flexible remote work options.

• Opportunities for skill enhancement.

• Chance to expand experience in various therapeutic areas.

• Potential to gain expertise in clinical research.