Key Responsibilities :
Conduct qualification, initiation, monitoring, and closeout visits for research sites complying with the approved protocol
Liaising with the medical site staff and coordinators
Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
Ensuring good documentation practices are being adhered to as per SOPs, GCP and applicable regulatory requirements.
What kind of person are we looking for?
Minimum 3 Years' experience as a Clinical Research Associate
Bachelor's degree in a Health or Science related field
Good time management and understanding of Clinical Trial Management
Excellent communication skills
If you are interested, kindly apply with your updated CV.