Sr. Clinical Research Associate

📋 Description

• Considered as the Primary Sponsor Point of contact for the investigative site.
• Advanced level of competency or experience in providing contextual information on the clinical
• Ability to motivate and align monitoring community through leadership and mentorship.
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
• Able to support, guide, and mentor junior personnel on Site Management activities.
• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific
• Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in
• Familiar with risk-based monitoring approach, onsite and offsite monitoring.
• Knowledge of appropriate therapeutic area indications with the ability to understand and apply
• Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP
• Demonstrate advanced communication skills and superior cross-functional collaboration skills among