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

📋 Description

• Oversee and direct clinical trial activities in accordance with protocols, regulatory guidelines, and industry standards.

• Lead monitoring tasks for clinical trials, emphasizing quality assurance and continuous improvement.

• Ensure clinical trial sites comply with study protocols, regulatory guidelines, and Good Clinical Practice (GCP) standards.

• Conduct site visits to evaluate performance, address issues, and facilitate successful execution of trials.

• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.

• Provide training and support to site staff and other Clinical Research Associates (CRAs).

• Establish and nurture relationships with site personnel and stakeholders.

• Operate within a sponsor-dedicated model focused on current Oncology monitoring.

⛳️ Requirements

• A Bachelor's degree in a relevant scientific discipline or a healthcare-related field.

• Significant experience as a Clinical Research Associate, demonstrating a robust understanding of clinical trial processes and regulatory guidelines.

• Proven capability to manage multiple sites and projects concurrently, showcasing strong organizational and problem-solving abilities.

• Proficiency in monitoring practices, data integrity, and site management, along with familiarity with pertinent clinical trial software and tools.

• Outstanding communication, interpersonal, and stakeholder management skills, with the ability to influence and enforce compliance in a complex environment.

• Willingness to travel as necessary (approximately 60%).

• Legal eligibility to work in Canada.