Senior Clinical Research Associate
$120,000–$150,000 year
RemoteCanada
Job Summary
Conduct and report SIV, RMV, and COV onsite monitoring visits, including CRF review, source document verification, and query resolution. Manage site communications, serve as a point of contact for in-house support and vendors, and communicate study progress to internal project teams. Participate in feasibility research, support regulatory document preparation for submissions, and prepare for audits and inspections. Requires independent on-site experience in Phase II and III studies, with Oncology experience preferred. Full English and French proficiency, valid driver's license, and ability to travel are necessary. This freelance role is based in Canada; PSI does not offer work visa sponsorship.
Required Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver's license
Desired Qualifications
- Experience in Oncology is a plus
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.