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.