Hina Shujat

Responsibilities:

• Screen, enrolls and recruits research participants.
• Reviews study participant medical history for inclusion/exclusion criteria.
• Assist with informed consent process and explains study to participants in easily understandable plain terms.
• Coordinates conducting subject’s study visits per protocol.
• Completes all study related approved procedures, questionnaires and follow- up visits.
• Assures research information is collected and stored in a manner that is complaint with regulations/ policies and good clinical practice.
• Recognizes adverse events, protocol deviations and other unanticipated problems and reports appropriately
• Ensure the quality of case report forms, maintain source documents.