Clinical Research Associate II - Oncology (Central Tennessee)

📋 Description

• Partners with the investigator and site staff for meaningful and effective engagements positioning
• Considered as the primary point of contact for the investigative site. High level of competency or
• 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 strategy for
• Advanced level of competency connecting the study protocol, scientific principles and clinical

🎯 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
• 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.
• Demonstrate strong planning and organizational skills and the ability to work effectively and