Clinical Trial Associate

A company is looking for a Clinical Trial Associate to oversee site management activities for clinical trials.

Key Responsibilities

Oversee day-to-day site management activities, ensuring compliance with study protocols and regulatory requirements

Collaborate with site staff and cross-functional teams to resolve issues and ensure timely data collection

Assist with site initiation, monitoring visits, and close-out activities while preparing and maintaining site management documentation

Required Qualifications

Bachelor's degree in life sciences, clinical research, or a related field

Extensive experience in site management, clinical operations, or monitoring within the clinical research industry

Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements

Ability to manage multiple sites and timelines effectively

Experience in providing guidance and mentorship to junior site management staff