Sr. Clinical Trial Associate
$65–$80,000 year
On-siteNew Brunswick, Canada
Job Summary
Support operational strategy and execution of clinical studies by managing study startup, site initiation, and regulatory inspection readiness. Approve study documentation, oversee risk-based monitoring, and prepare materials for regulatory inspections. Collaborate with the Clinical Operations Manager, study teams, CROs, and vendors to facilitate contracts, meetings, and vendor administration. Escalate clinical trial insurance issues and attend important team meetings. Perform developmental tasks with oversight from the CTA Manager. Requires 5+ years in pharma or clinical research, experience with Phase 2 and 3 studies, and 5-10% domestic and international travel.
Required Qualifications
- Bachelor's degree or equivalent international degree
- 5 or more years' experience in pharmaceutical industry, clinical research organization, or related role
- Requires availability for 5-10% domestic and international travel, including overnight and international travel on an as-needed basis
Desired Qualifications
- Experience in Phase 2 and 3 studies and global/international studies is advantageous
- Experience working across multiple therapeutic areas is advantageous
- Knowledge in global regulatory and compliance requirements for clinical research
- Excellence in task management and collaboration
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.