Senior Clinical Research Associate

📋 Description

• Act as primary sponsor point of contact for investigative sites, providing contextual information
• Motivate and align the monitoring community through leadership and mentorship.
• Align, train, and motivate site staff and principal investigator on the goals of the clinical trial
• Conduct site evaluation, site training, routine on-site and off-site monitoring, and site closure
• Customize site engagement strategies, gather site insights, and report progress using engagement
• Connect study protocol, scientific principles, and clinical trial requirements to daily execution

🎯 Requirements

• Bachelor's degree or equivalent; health-related field preferred (Medical, Scientific, Nursing
• Minimum of 3 years of clinically related experience, with at least 2 years in independent clinical
• Deep understanding of therapeutic area indications to apply scientific concepts in clinical trials.
• Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies.
• Advanced communication and cross-functional collaboration skills.
• Strong planning, organizational, and time-management skills in a dynamic environment.