Join our team and help shape the future of our organization by supporting growth through clinical study site management
Job Summary
Join our team and help shape the future of our organization by supporting growth through clinical study site management.
Perform site monitoring visits in compliance with GCP and ICH guidelines and manage study progress including regulatory submissions and data quality.
Be part of an innovative and forward-thinking company that offers many opportunities for professional growth and a competitive salary and benefits package.
Matching Summary
Join our team and help shape the future of our organization by supporting growth through clinical study site management.
Skills & Requirements
Must-have
site monitoring visits
Good Clinical Practice (GCP)
International Conference on Harmonization (ICH)
clinical research regulatory knowledge
protocol adherence monitoring
study data reporting
Microsoft Office proficiency
Nice-to-have
strong attention to detail
excellent communication skills
problem-solving abilities
organizational skills
time and financial management
effective working relationships
Key Requirements
Bachelor's Degree in scientific discipline or health care
Excellent command of English
Knowledge of clinical research regulations
Experience with protocol and therapeutic knowledge