Clinical Research Associate I

📋 Description

• Considered as the primary point of contact for the investigative site, provides contextual
• Aligns, trains and motivates the site staff and principal investigator under supervision on the
• Conducts site evaluation, site training, routine, and site closure monitoring activities under
• Customize site engagement strategy for assigned study(ies) under supervision. Gather local/site
• Fundamental level of competency connecting the study protocol, scientific principles and clinical
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient

🎯 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 preferable in
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand
• Knowledge on 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