Site Start-Up & Activation Associate (FSP) at PAREXEL

Position Purpose

The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and per prevailing laws, Good Clinical Practices, and Client standards.

Responsibility within a country may span over more than 1 country depending on the geographical region and business needs.

Key skills required to be considered for the role:

• School diploma/certificate with an equivalent combination of education, training, and experience; Bachelor of Science, Bachelor of Arts, or Bachelor’s in Life Sciences preferred.
• Minimum of 2 years relevant experience in clinical site management
• Experience working in the pharmaceutical industry/or CRO in study site activation is preferred.
• Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations.
• Demonstrated knowledge of clinical research and development processes, Key operational elements of a clinical trial, and ability to gain command of process details.
• Knows GCP requirements and is proficient in computer operations.
• Must be fluent in English.