Clinical Trials Associate

Job Summary

A company is looking for a Clinical Trials Associate to manage clinical trials administration and support clinical research studies.

Key Responsibilities

• Support Clinical Operations teams in completing tasks to meet trial and project goals
• Maintain and organize clinical study documentation, preparing for audits and reconciliations
• Collaborate with CTM and CRAs to resolve documentation issues and facilitate site communications

Required Qualifications

• Bachelor's degree with 0-2 years of clinical research experience or a high school diploma with 5+ years of clinical research experience
• Proficiency in MS Word, Excel, PowerPoint, Outlook, and Adobe
• Knowledge of good documentation practices (GDP)
• Ability to maintain corporate confidentiality
• Experience with clinical trial documentation and compliance processes