Clinical Research Associate I

📋 Description

• Primary Sponsor point of contact for the investigative site, providing contextual information on
• Aligns, trains, and motivates the site staff and principal investigator with support as needed on
• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure
• Customize site engagement strategy for assigned study(ies) with support as needed, gather
• Fundamental level of competency connecting the study protocol, scientific principles, and clinical
• Develop solid knowledge of therapeutic area, asset, and clinical landscape/patient journey to

🎯 Requirements

• Bachelor's degree or equivalent degree; health-related preferred (e.g. Medical, Scientific
• Clinically related experience, in clinical research coordinating or data management preferred.
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand
• Knowledge of existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines, and
• Able to work collaboratively and cross-functionally to develop and sustain working relationships.
• Demonstrate planning and organizational skills and the ability to work effectively and efficiently