Clinical Trial Associate

📋 Description

• Support clinical trial operations across all phases of the study lifecycle, ensuring milestones
• Assist with CRO and vendor coordination and oversight, including tracking performance
• Collect, track, and review investigator site regulatory documentation (e.g., FDA Form 1572, FDFs
• Manage Trial Master File (TMF) filing, maintenance, reconciliation, and inspection readiness
• Track and maintain essential study documentation, including CTA and budget status, site and vendor
• Coordinate study team, vendor, and site meetings, including scheduling, agenda preparation

🎯 Requirements

• Ability to work in a matrix environment
• Experience working in a high-volume environment while maintaining both organization and the ability
• Good understanding of the responsibilities and needs of other functions in a clinical trial
• Reliable, conscientious, and confidential
• Strong interpersonal skills and ability to deal with people at all levels with sensitivity and tact
• Some experience in oncology

🎁 Benefits

• Career advancement/ development opportunities
• Competitive comp package
• Bonus
• 401K + Employer contributions
• Generous stock options
• ESPP Plan