As an Associate Site Manager, you will be the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and regulations
Job Summary
As an Associate Site Manager, you will be the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and regulations.
Responsibilities include assisting with site selection, qualification, initiation, monitoring (on-site and remote), and close-out activities, partnering with the Local Trial Manager and other team members.
This role requires a BA/BS degree in a related field, 1+ year of clinical trial monitoring experience, strong IT skills, and proficiency in the country language and English.
Matching Summary
As an Associate Site Manager, you will be the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with protocols, SOPs, GCP, and regulations.
Skills & Requirements
Must-have
GCP, SOPs, and applicable regulations
Site initiation and start-up
On-site and remote monitoring
Subject recruitment and retention planning
Data entry and query resolution
Nice-to-have
Therapeutic area experience
Process improvement contributions
Building good working relationships
Key Requirements
1-2 years of clinical trial monitoring experience
BA or BS degree in Pharmacy, Nursing, Life Sciences, or related scientific field
Proficient in speaking and writing the country language and English