The Site Coordinator will be delegated in performing assigned Site Study tasks, working to facilitate the Principal Investigator (PI) job, contributing to the quality of the study, providing appropriate support to reach the milestones, pro-actively recruiting new patients and speeding up any data-entry process
Job Summary
The Site Coordinator will be delegated in performing assigned Site Study tasks, working to facilitate the Principal Investigator (PI) job, contributing to the quality of the study, providing appropriate support to reach the milestones, pro-actively recruiting new patients and speeding up any data-entry process.
As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.
We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.
Matching Summary
The Site Coordinator will be delegated in performing assigned Site Study tasks, working to facilitate the Principal Investigator (PI) job, contributing to the quality of the study, providing appropriate support to reach the milestones, pro-actively recruiting new patients and speeding up any data-entry process.
Skills & Requirements
Must-have
Data Entry
Queries resolution
SAE notification
Patient recruitment assistance
Ethics Committee submissions
Investigator File updating
Patient visits schedule
Study Drug Accountability
Sample Management
Nice-to-have
Collaboration
Quality focus
Making a difference
Flexibility
Sustainability
Key Requirements
Clinical or life science background
GCP certification
Site coordination experience
eCRF / EDC system familiarity
Strong administration and document management skills