Clinical Research Associate II

📋 Description

• Considered as the primary point of contact for the investigative site.
• High level of competency or experience in providing contextual information on the clinical trials
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
• Conducts site evaluation, site training, routine, and site closure monitoring activities with
• Advanced understanding of site engagement and ability to customize site engagement for assigned
• Gather local/site insights and utilize site engagement tools such as the Customer Relationship

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
• Minimum of 1 year of clinically related experience, of which a period of 6 months is required in
• Familiar with risk-based monitoring approach, onsite and offsite monitoring.
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand
• Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP
• Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.