Duties and Responsibilities
• Support the day-to-day implementation of research activities in accordance with approved study protocols, standard operating procedures (SOPs), work plans and ethical requirements.
• Assist with planning and coordinating field activities, including preparation of study materials, schedules, logistics and site visits.
• Support participant identification, screening, recruitment, enrolment, informed consent, follow-up and retention in accordance with study procedures.
• Conduct quantitative and qualitative data collection using approved tools, including questionnaires, interviews and electronic data collection platforms.
• Ensure accurate, complete and timely data entry, verification, management and submission, including routine data quality checks and resolution of queries.
• Maintain accurate and confidential study records, including participant information, consent forms, field activities and intervention documentation.
• Support implementation and monitoring of study interventions, including training, supervision, commodity distribution and use of digital platforms, where applicable.
• Liaise with participating institutions, healthcare providers, community stakeholders and study teams to facilitate research activities.
• Conduct routine monitoring and quality assurance visits, document implementation challenges and report findings to the supervisor.
• Assist in preparing routine progress reports, study updates, meeting minutes and other research documentation.
• Ensure compliance with research ethics, participant confidentiality, data protection and safety requirements, including timely reporting of adverse events and protocol deviations.
• Perform other research-related duties assigned by the supervisor Donateto Research


Qualifications and Experience
Bachelor’s degree in social sciences, or a related field, A valid Good Clinical Practice Certificate before commencement of work. At least one year experience in research implementation, participant recruitment, informed consent, follow-up or data collection, Experience working in HIV prevention, sexual and reproductive health, community health or related research programmes. Experience working respectfully with adolescents, young adults and/or key or underserved populations is desirable, Experience with electronic data collection systems such as Redcap, ODK or SurveyCTO, or other mobile health platforms, is an advantage. good interpersonal and communication skills, both oral and written; proficiency in Microsoft Office packages and electronic data collection and mHealth systems; strong planning, problem-solving and organisational skills; understanding of Good Clinical Practice (GCP) and research ethics; good report-writing skills; ability to manage multiple activities across study sites; and commitment to participant confidentiality, safeguarding, ethical conduct and the protection of sensitive information. SearchJobs