Research Assistant (Emirati)

Responsibilities

• Identify and screen potential study participants based on inclusion and exclusion criteria as outlined in the study protocol.
• Obtain informed consent from participants, ensuring they fully understand the study's purpose, procedures, and potential risks and benefits.
• Assist in data collection and ensure accurate entry of study data into electronic data capture systems and clinical databases.
• Maintain detailed and organized records of study related activities, including patient information, consent forms, and other relevant documents.
• Conduct regular data quality checks to ensure accuracy and completeness of collected data.
• Schedule study visits and follow ups with participants, coordinating with clinical staff as needed.
• Provide support to study participants throughout the study process, addressing any questions or concerns as needed.
• Follow study protocols and standard operating procedures (SOPs) to ensure compliance with regulatory and ethical standards.
• Assist in preparing and maintaining regulatory documents, including IRB submissions, amendments, and approvals.
• Work closely with principal investigators and research teams to support study objectives and ensure seamless operations.
• Communicate regularly with the research team about study progress, participant status, and any issues that arise during the study.
• Ensure all study procedures are conducted according to protocol and SOPs, contributing to the overall quality and integrity of the research.