Associate Site Manager serves as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines
Job Summary
Associate Site Manager serves as the primary contact point between the Sponsor and the Investigational Site, ensuring 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).
The role requires strong working knowledge of GCP, company SOPs, local laws and regulations, and assigned protocols, with a willingness to travel and proficiency in both the country language and English.
Matching Summary
Associate Site Manager serves as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines.
Skills & Requirements
Must-have
GCP compliance
protocol adherence
site initiation and close-out
remote monitoring
regulatory compliance
Nice-to-have
process improvement
mentoring
therapeutic area expertise
proactive behavior
problem solving
Key Requirements
Minimum 1 year clinical trial monitoring experience preferred
BA or BS degree in Life Sciences, Nursing or related scientific field
Proficient in speaking and writing country language and English