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.
• Key responsibilities include data entry, queries resolution, assisting with SAE notification, helping investigator with patient recruitment, and facilitating Ethics Committee submissions.
• The company offers opportunities for personal and professional growth in a rewarding environment within a team that values collaboration, quality, and making a difference in the lives of patients.

Matching Summary

Skills & Requirements

Key Requirements

• Clinical or life science background
• GCP certification
• Site coordination experience
• eCRF / EDC system familiarity
• Strong administration and document management skills
• Local language mandatory (Danish)
• Comfortable working across several sites

Work Rights