Clinical Trials Associate

Job Summary

A company is looking for a Clinical Trials Associate responsible for clinical trials administration to ensure the effective 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, including preparation for audits and archival
• Collaborate with Clinical Trials Manager and Clinical Research Associates to resolve documentation issues

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 (GDocP) and good documentation practices (GDP)
• Ability to maintain corporate confidentiality at all times
• Experience in clinical trial documentation and site management is preferred