Sr Clinical Research Associate

Act as a subject matter expert, mentor, coach, and/or provide performance feedback to the manager for peers in clinical research roles.

Assist with the selection, hiring, training, and supervision of Clinical Research Associates (CRAs) as needed. Perform co-monitoring and training visits with CRAs.

When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns.

May represent the Director, Monitoring and Site Management or Manager, Clinical Site Management in business development (BD) initiatives with a site monitoring focus.

May be assigned a Lead CRA role and manage monitoring services for a group of projects and/or CRAs on large/complex projects, including directing/guiding day-to-day activities and reviewing/approving monitoring reports.

Oversee the overall integrity of the study to promote positive working relationships with the site and staff.

Ensure Standard Operating Procedures (SOPs) are in place to optimize patient recruitment, providing guidance to site teams on inclusion/exclusion criteria.

Qualifications

• Applicants should have relevant clinical monitoring experience, with Senior CRA candidates expected to have several years of progressive on-site and/or remote monitoring experience across multi-centre clinical trials.
• A valid driving license may be required depending on site coverage needs.