Job descriptionAssist with the recruitment and screening of study participants.Schedule and coordinate study visits and follow-ups.Collect and record data accurately in study databases or case report forms (CRFs).Obtain and process informed consent from participants.Maintain and organize study files and documents.Support the Principal Investigator and research team in regulatory and administrative tasks.Communicate with participants, sponsors, and other research staff as needed.Ensure compliance with Good Clinical Practice (GCP) and all applicable regulations.