Clinical Trials Associate

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