Main Duties and Responsibilities ● Assist with participant screening, recruitment, eligibility assessment, informed consent, and follow-up. ● Collect, enter, organize, and verify clinical research data accurately. ● Maintain study documents, participant files, screening logs, consent forms, and regulatory records. ● Conduct literature reviews and assist with research protocols, reports, abstracts, presentations, and manuscripts. ● Support data analysis and preparation of tables, figures, and study summaries. ● Coordinate with investigators, clinical staff, research participants, and other study team members. ● Ensure that all research activities comply with the approved protocol, Good Clinical Practice, ethical requirements, confidentiality standards, and institutional policies. ● Assist with ethics submissions, study amendments, progress reports, and other administrative research requirements. ● Attend research meetings and provide regular updates on study progress. ● Perform any other research-related duties assigned by the Principal Investigator.

● Bachelor of Medicine and Bachelor of Surgery or another relevant healthcare qualification. ● Previous experience in clinical research, data collection, literature review, and manuscript preparation. ● Knowledge of Good Clinical Practice and research ethics. ● Strong communication, organizational, and teamwork skills. ● Ability to maintain accurate records and protect confidential participant information. ● Proficiency in Microsoft Office and research-related software.

● Bachelor of Medicine and Bachelor of Surgery or another relevant healthcare qualification. ● Previous experience in clinical research, data collection, literature review, and manuscript preparation. ● Knowledge of Good Clinical Practice and research ethics. ● Strong communication, organizational, and teamwork skills. ● Ability to maintain accurate records and protect confidential participant information. ● Proficiency in Microsoft Office and research-related software.

3550

30/09/2026