Clinical Trial Associate

Premier Research • Regional_NC, NC

2d

About The Position

Premier Research is looking for a Clinical Trial Associate to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here.

Requirements

• Bachelor’s degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience
• 0-2 years of practical experience with clinical trial administration (e.g. – Inhouse CRA, CTA, site administration, project coordination) preferred
• Ability to adapt and work on multiple tasks to assist study teams and/or sponsor with various tasks within clinical research highly preferred
• Strong ability to communicate effectively with sponsor, study teams and vendors to achieve deadlines for task assigned is ideal
• Strong analytical and organization skills, able to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities highly preferred

Responsibilities

• Works with Clinical Team Trial Execution team to assist with specific study start up tasks for studies.
• Coordinates logistics and planning of meeting, events, and training
• Primary lead to disseminate announcements and training materials related to clinical system updates and enhancements, as required
• Co-Leads and participates in project team meetings, prepares meeting minutes, and maintains action/decision logs
• Create, maintain and provide quality checks for tracking tools and database repositories for operational data including Key Performance Indicators (KPIs) and quality metrics
• Performs Clinical Inspection Readiness and Quality Management System activities (e.g., deviations and CAPAs)

Benefits

• health insurance
• retirement plans
• paid time off

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level