Job Summary: The Senior Research Officer will work closely with a multidisciplinary team of Principal Investigators and Co-investigators to lead in evaluating and documenting insights through qualitative methods for programs being implemented at ICRH The incumbent will lead in the development of research protocols, designing qualitative data collection tools, training and supervising field research assistants. Further, the Officer will coordinate transcribers, and conduct qualitative data analysis and summary reports.
Qualitative Research data collection & analysis
Support in designing and pre-testing data collection tools
Train research assistants on qualitative data collection techniques, and supervise and offer technical assistance during field data collection
Guiding the research assistants through the process of contacting/identifying research participants, screening for eligibility, informed consent, and data handling techniques
Lead in transcription, translation, and analysis of qualitative data
Compile the study findings by preparing comprehensive qualitative summaries
Ensure safe transmission, storage, and archiving of qualitative data and scripts
Coordination of project/study activities
Co-ordinate day-to-day activities of the projects by establishing and maintaining a project work plans
Establish relationships with relevant stakeholders in the study areas
Take the lead in preparing reports for rapid learning to the implementing partners and the donors
Participate in the final study reports
Participate in the recruitment and supervision of research assistants in the study areas
Prepare for the training of research assistants; prepare training materials etc. organize logistics related to the training venue, trainers, transport reimbursement etc.
Perform other duties and responsibilities as assigned by the supervisor and ICRHK management
Research plan development
Conduct background literature reviews, author sections relevant to the protocols and coordinate with the PIs and other investigators to ensure the protocols are submitted to the ethics committee on time
Perform regular review of the regulatory binder to ensure valid research certificates and valid Good Clinical Practices (GCP) certificates for all staff involved in the projects.
Ensure all study documents are handled and stored in accordance to data handling and protection guidelines
Essential Requirements
Education: Master’s degree in medical anthropology, medical sociology, public health or a related field emphasizing qualitative research methods training
5+ years with professional qualitative research experience
3+ years conducting in-depth interviewing, focus group discussions, and participant observation
Knowledge and understanding of public health issues and human subjects protocols
Experience working with stakeholders to design, author, and manage qualitative studies
Strong organizational, planning, and problem-solving skills
Strong interpersonal skills and a team player
Strong report-writing skills
Proficiency with any of the following qualitative software: NVivo, Atlas, Nudist, and citation software such as EndNote
Excellent written, verbal, and visual communication skills required
Apply via :
mail.icrhk.org
