Senior Clinical Research Associate

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

📋 Description

• Conduct and report on-site monitoring visits for SIV, RMV, and COV.

• Execute CRF reviews, verify source documents, and resolve queries.

• Oversee site communication and management.

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

• Update internal project teams on study progress.

• Engage in feasibility assessments.

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

• Prepare for and take part in audits and inspections.

⛳️ Requirements

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

• Experience in independent on-site 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.

• Proficient in MS Office applications.

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

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

• Willingness to travel.

• Valid driver's license.

• Must not require work visa sponsorship for current or future employment.

🏝️ Benefits

• Option for remote work.

• Chance to further enhance skills.

• Opportunity to expand therapeutic area experience.

• Potential to become an expert in clinical research.