This role serves as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and applicable regulations
Job Summary
This role serves as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and applicable regulations.
Responsibilities include assisting with site selection, subject recruitment, site initiation, monitoring, and close-out activities, partnering with the Local Trial Manager and other team members.
The Senior Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) to ensure overall site management while performing trial related activities for assigned protocols.
Matching Summary
This role serves as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and applicable regulations.
Skills & Requirements
Must-have
Good Clinical Practice (GCP)
company Standard Operating Procedures (SOP)
clinical trial protocol compliance
site initiation and start-up
on-site and remote monitoring
subject recruitment and retention planning
Nice-to-have
process improvement contributions
training and mentoring capabilities
therapeutic area experience
Key Requirements
3-5 years of experience
BA or BS degree in Pharmacy, Nursing, Life Sciences or related scientific field
2 years of clinical trial monitoring experience
Proficient in speaking and writing the country language and English