Research Assistant

Assist doctors and researchers in designing, conducting, and analysing clinical and laboratory research projects related to ophthalmology. Collect, organize, and maintain research data, ensuring accuracy and integrity in data management. Provide statistical support using appropriate software (e.g., SPSS, R, Excel) to analyse clinical data. Assist in preparing research reports and presentations, including the organization of data for visual representation. Schedules study participant appointments and serves as the patient liaison to the Principal Investigator (PI) and other participating consultants. Collecting study data from EMR and other instruments of participants of clinical studies being carried out in the department Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections. Working closely with the PI, participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process. Conducting clinical tests for study participants at pre-operative and scheduled post operative visits. Assist in coordinating and managing CME, workshops, and seminars. Guide students with their thesis, ensuring they follow proper research methodology, data collection, and analysis techniques. Provide mentorship and support to students in preparing research proposals and projects, ensuring compliance with ethical standards. Assist students in writing, formatting, and reviewing research papers, theses, and dissertations. Help doctors and researchers in the publication process, including drafting, reviewing, and formatting research papers for peer-reviewed journals, CTRI registration. Provide guidance on manuscript preparation, citation management, and addressing reviewer comments. Assist in preparing clinical presentations and posters for academic and professional conferences. Ensure proper referencing and adherence to publication standards and guidelines. Co-ordinate with Biostatistician for conduct of statistical analysis of clinical trial data, patient outcomes, and other research-related data. Create and maintain databases for research purposes and provide regular updates to researchers. Ensure that all research activities comply with ethical guidelines and institutional ethics committee requirements. Assist with the preparation and submission of research protocols, ethical reviews, and consent forms. Maintain accurate and up-to-date records of research activities, publications, and educational programs. Collaborate with ophthalmologists, optometrists, nurses, and other healthcare supportive staff to ensure smooth implementation of research projects. Facilitate communication between the research team and other hospital departments to ensure the timely collection of data. Assist in organizing clinical trials, ensuring proper patient recruitment, informed consent, and adherence to research protocols. Stay updated with the latest research trends, statistical tools, and technological advancements in ophthalmology and research methodologies. Participate in training sessions, conferences, and seminars to enhance skills and knowledge in the field of ophthalmic research.