Senior Clinical Research Associate (West Coast based)

📋 Description

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit
• Identifies the investigators and verifies that the investigator has adequate qualifications
• Trains investigational site staff as necessary
• When applicable, supports preparation of regulatory and / or EC submissions
• Participates in mentoring/training of new staff as well as performing co-monitoring visits, to

🎯 Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex
• Full working proficiency in English
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel nationally