Serve as the primary liaison between Novartis and assigned investigational sites
Conduct Site Initiation, routine monitoring (on‑site and remote), and Close‑Out visits as per Monitoring Plan
Ensure compliance with protocol, ICH/GCP, regulatory requirements, and Novartis SOPs
Proactively identify site risks, issues, and deviations; drive timely mitigation and resolution
Build strong site partnerships to optimize patient recruitment, flow, and site performance
Ensure accuracy, completeness, and timeliness of site documentation and sTMF
Support audit and inspection readiness and implement CAPAs within agreed timelines
Collaborate cross‑functionally with CPMs, CRA Managers, Medical, MSLs, and other stakeholders

Degree in a scientific or healthcare discipline (or equivalent relevant experience).
Minimum 4 years of pharmaceutical or clinical research experience
Hands-on experience in site monitoring and clinical trial execution
Strong knowledge of ICH/GCP , regulatory requirements, and clinical trial processes
Ability to manage sites independently with strong decision‑making capability
Proficient written and spoken English and local country language
Willingness and ability to travel extensively (including overnight travel)

Senior Clinical Research Associate

Key skills