Senior Clinical Research Associate

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

📋 Description

• Carry out and document SIV, RMV, and COV onsite monitoring visits.

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

• Oversee site communication and management efforts.

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

• Interact with internal project teams to update them on study progress.

• Engage in feasibility assessments.

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

• Prepare for and take part in audits and inspections.

⛳️ Requirements

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

• Experience in independent onsite monitoring.

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

• Experience in Oncology is advantageous.

• Fluency in both English and French is crucial.

• Competence in MS Office applications.

• Capable of planning, multitasking, and thriving in a fast-paced team environment.

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

• Willingness to travel.

• Possession of a valid driver’s license.

🏝️ Benefits

• Chance to enhance skill sets.

• Opportunity to broaden therapeutic area experience.

• Potential to become a specialist in clinical research.

• Option for remote work.