Job Summary

• A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines.
• Responsibilities include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring, and close-out activities, partnering with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM).
• Establishes and maintains good working relationships with internal and external stakeholders, particularly investigators, trial coordinators, and other site staff, and may participate in Health Authority (HA) and IEC/IRB submission and notification processes.

Matching Summary

Skills & Requirements

Key Requirements

• BA or BS degree in Life Sciences, Nursing or related scientific field
• 1 year clinical trial monitoring experience preferred
• Strong working knowledge of GCP, company SOPs, local laws and regulations
• Proficient in speaking and writing the country language and English

Work Rights