Clinical Trials Associate

Job Summary

A company is looking for a Clinical Trials Associate responsible for clinical trials administration to ensure effective and efficient conduct of clinical research studies.

Key Responsibilities

• Support Clinical Operations teams in completing tasks to meet trial and project goals
• Maintain and organize clinical study documentation, ensuring compliance with regulations and practices
• Collaborate with team members to resolve clinical trial documentation issues and facilitate communication with clinical sites

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