Senior Clinical Research Associate

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

📋 Description

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

• Carry out CRF reviews, verify source documents, and resolve queries.

• Manage communication and foster relationships with site staff.

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

• Update internal project teams on the progress of studies.

• Engage in feasibility assessments.

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

• Prepare for and participate in audits and inspections.

⛳️ Requirements

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

• Proven 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 English is required.

• 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 as needed.

• A valid driver’s license is essential.

• Must not require work visa sponsorship for employment now or in the future.

🏝️ Benefits

• Option for remote work.

• Opportunity for skill enhancement.

• Chance to broaden therapeutic area experience.

• Potential to become a specialist in clinical research.