Clinical Research Associate, Site Management - Italy

The Clinical Research Associate, Site Management role involves conducting clinical monitoring visits, training, and site management in accordance with study protocol and regulatory requirements.

Requirements

• Bachelor's Degree in scientific discipline or health care
• In possession of local ministerial decree requirements as per Italian law
• At least 1 year prior clinical experience preferred
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Written and verbal communication skills including good command of English language
• Organizational and problem-solving skills
• Effective time and financial management skills
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of applicable protocol requirements as provided in company training