Clinical Trials Associate

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