Clinical Trials Associate

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