Primary point of contact for the investigative site
Aligns, trains and motivates the site staff and principal investigator on clinical trial goals
Conducts site evaluation, training, routine, and closure monitoring activities
Develops site engagement strategies and uses CRM tools
Evaluates recruitment and retention techniques based on patient disease journey
Mentors and trains less experienced CRAs

🎯 Requirements

Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
Minimum of 1 year of clinically related experience, with 6 months in clinical research monitoring
Knowledge of appropriate therapeutic area indications preferred
Advanced knowledge of local regulatory requirements, ICH/GCP Guidelines
Strong cross-functional collaboration skills
Strong planning and organizational skills

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