Education: - MBBS - Essential. - PhD Degree in related field - Preferred. Work Experience: - Minimum of 7 (Seven) years position related practical experience in clinical research process and scientific methods -Essential. Competencies: - Experience in research medical writing - Essential. - Proven clinical research skills - Essential. - Ability to communicate effectively -Essential. - Ability to work with a team - Essential. - Ability to develop others - Essential.
- Responsible for providing assistance to Principal Investigators/Scientists by coordinating , participating and working on scientific clinical research activities/projects, assisting and monitoring subordinate staff within the research team and ensuring that the laboratory areas are well maintained and the conduct of research is in line with the appropriate regulating bodies, accrediting standards and relevant policies and procedures. - Coordinate with the Principal Investigators to initiate map and plan research projects; and keep progress updates and reports. May participate actively on research projects as Principal Investigator or Co-Principal Investigator. - Coordinate and validate quantitative data files, evaluating the quality of data and describe data structure, to enhance control of data. - Monitor data collection process from patient charts, medical records, interviews, questionnaires, diagnostic test and other sources, review and implement collections procedures, evaluate and interpret collected data and assure appropriate documentation and presentation. - Control input of data into the research database. Draw the necessary reports and records for audits and any other ad hoc requirements. - Perform a variety of tasks using methods and procedures and established laboratory techniques on both manual and automated equipment. - Provide assistance in conducting training. - Participate in preparation of personnel evaluations, attend and participate in meetings, conferences and training group as required. - Liaise the activities of research office with other sections of KAIMRC and other respective departments within MNGHA on a regular basis to ensure smooth and effective operations. - Compile processes and analyze data, record research procedures and results; file and maintain records; code data for input for electronic data processing. - Monitor quality assurance. - Perform other job related duties.
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