Patient Recruitment:• Identify and screen potential study participants based on inclusion and exclusioncriteria as outlined in the study protocol.• Obtain informed consent from participants, ensuring they fully understand thestudy's purpose, procedures, and potential risks and benefits.Data Collection:• Assist in data collection and ensure accurate entry of study data into electronic data capture systemsand clinical databases.• Maintain detailed and organized records of study-related activities, including patientinformation, consent forms, and other relevant documents.• Conduct regular data quality checks to ensure accuracy and completeness of collected data.Participant Interaction:• Schedule study visits and follow-ups with participants, coordinating with clinical staff asneeded.• Provide support to study participants throughout the study process, addressing anyquestions or concerns as needed.Compliance and Regulatory:• Follow study protocols and standard operating procedures (SOPs) to ensure compliancewith regulatory and ethical standards.• Assist in preparing and maintaining regulatory documents, including IRB submissions,amendments, and approvals.Communication and Collaboration:• Work closely with principal investigators and research teams to support study objectivesand ensure seamless operations.• Communicate regularly with the research team about study progress, participant status,and any issues that arise during the study.Quality Assurance:• Ensure all study procedures are conducted according to protocol and SOPs, contributing tothe overall quality and integrity of the research.• Assist in preparing for audits and inspections by maintaining accurate and up-to-date studydocumentation.
Bachelor’s degree in health sciences, Nursing, Biology,Psychology, or a related field.
Minimum of 1 year of experience in clinical research setting orrelated field.