Qualitative Research Assistant

Malaria Consortium

Sokoto, Nigeria

Malaria Consortium (MC) is implementing an embedded implementation research study in selected local government areas (LGAs) of Kogi, Plateau and Sokoto States to assess approaches for linking routine immunization (RI) activities with Seasonal Malaria Chemoprevention (SMC) delivery. The approaches comprise: A, structured RI messaging during SMC contact; B, Approach A plus community engagement/social and behaviour change communication (SBCC); and C, Approach B plus immunization-status screening, referral and follow-up. A comparator arm receives standard SMC. The qualitative component explores acceptability, feasibility, implementation burden, fidelity, perceived effectiveness, equity and scalability. MC seeks six state-based Research Assistants (RAs), two in each state, and other state-level data collection team members (Moderators, Notetakers and qualitative data transcribers) to support the approved qualitative fieldwork. The RAs will work under the day-to-day technical direction and supervision of the Lead Qualitative Research Consultant and within MC-approved study procedures. We are recruiting to fill the position below: Job Title: Qualitative Research Assistant Locations: Silame, Shagari, and Binji - Sokoto Purpose and limits of the assignment To engage and deploy four complementary cadresState Research Assistants, Qualitative Data Moderators, Note Takers and Qualitative Data Transcribersto undertake approved state-level qualitative fieldwork. Research Assistants coordinate recruitment, scheduling, field logistics and quality monitoring; Moderators conduct FGDs/KIIs; Note Takers document sessions and support debriefs; and Transcribers produce accurate, de-identified transcripts and approved translations. All cadres work under the technical supervision of the Lead Qualitative Research Consultant and Malaria Consortium (MC) oversight. This ToR covers field personnel only. No cadre is engaged to independently design or amend the protocol, approve sampling changes, lead the consultancy, undertake study-wide qualitative analysis, or prepare the final integrated research report. Duties are allocated by cadre and may overlap only when specifically assigned, personnel are trained and competent, and the Lead Consultant authorises the arrangement. Qualitative Study Participants and Planned Sample The Lead Qualitative Research Consultant will operationalize the approved multi-stage sampling process with MC and government counterparts. State Research Assistants will implement the approved recruitment plan and coordinate scheduling; Moderators and Note Takers will support eligibility checks and consent within their training and assigned roles; Transcribers will work only with authorised, consented recordings. No field cadre may independently change the sampling frame or respondent targets. Participant Identification and Recruitment The Research Assistants, based in Kogi, Plateau and Sokoto States, with the support of the moderators, Note takers and transcribers will coordinate participant identification and recruitment for qualitative data collection in their respective states, working closely with Malaria Consortium (MC), State Programme Managers and relevant state/LGA authorities to facilitate official introductions, access to selected clusters and model facilities, and participant mobilisation through appropriate community and programme structures. The Research Assistants with the support of the moderators, Note takers and transcribers will coordinate the implementation of the MC-approved sampling and recruitment plan, ensuring that approved recruitment lists and eligibility criteria are followed. They will oversee the screening process, maintain accurate screening and recruitment logs, monitor recruitment progress and support the selection of participants representing diverse roles, geographical locations and levels of intervention exposure. The Research Assistants will coordinate with trained qualitative data collectors to ensure that prospective participants are approached appropriately, eligibility is verified, and recruitment and informed consent procedures comply with the approved study protocol and ethical requirements. Recruitment and consent will be undertaken by trained research personnel who are not directly responsible for providing services to prospective participants to minimize potential coercion and power imbalances. The Research Assistants will coordinate the identification, recruitment and scheduling of the relevant respondent groups in their respective states, including caregivers and community drug distributors (CDDs) from the selected qualitative cluster in each intervention LGA; health workers from model facilities serving the selected clusters; community/traditional leaders in the three Approach C LGAs; and programme stakeholders purposively selected based on their responsibilities for SMC, routine immunization (RI), primary healthcare (PHC) planning, implementation, supervision or oversight. The Research Assistants will monitor recruitment against the approved state-level targets and data collection schedule, document recruitment challenges, ineligibility and non-response, and promptly communicate any proposed respondent replacements to the study lead and MC for review and approval. MC will retain final approval of the recruitment matrix and any replacement of a selected respondent. Supervision and working relationships The Lead Qualitative Research Consultant provides direct technical supervision to all four field cadres, including orientation, daily task allocation, coaching, fieldwork review, transcription standards and approval of routine adjustments within the MC-approved plan. Research Assistants coordinate state-level scheduling and day-to-day communication, but do not replace the Lead Consultant as technical supervisor. Research Assistants submit consolidated state updates; Moderators submit session completion records and interview issues; Note Takers submit session notes and debrief records; and Transcribers submit transcripts and discrepancy logs. Each cadre must promptly report consent, safeguarding, confidentiality, security or quality concerns to the Lead Consultant, with escalation to MC under approved procedures. MC retains overall authority for protocol, ethics, safeguarding, data governance, participant reimbursement and material changes to sampling or field procedures. MC/state/LGA counterparts support official introductions, access and approved mobilisation. No cadre may independently substitute participants, alter approved reimbursement or disclose study data. RAs and other data collection team members do not independently approve protocol changes, substitute respondents, alter reimbursement arrangements or share research data outside authorised channels. Responsibilities of each Research Assistant Review the approved protocol, assigned respondent guides, information sheets/consent forms, recruitment plan and state-specific field schedule; attend training and the field pre-test as directed. Prepare and maintain a state-level workplan and daily schedule under the Lead Consultant’s direction; coordinate with the second RA in the state to avoid duplication and ensure coverage. Liaise with approved state/LGA, health-facility and community contacts to arrange access, private venues and appropriate recruitment, without creating coercion or promising incentives. Screen and recruit eligible participants against approved criteria; document refusals and non-response; arrange FGDs and KIIs; obtain and document informed consent and separate audio-recording consent in accordance with the approved procedures. Facilitate or assist with FGDs/KIIs, probing and note-taking as assigned by the Lead Consultant, using the correct respondent-specific guide and intervention-approach routing. Check session records, audio quality (where consented), field notes, respondent IDs, dates and metadata; complete same-day debriefs and implement corrective actions requested by the Lead Consultant. Maintain a rolling recruitment and fieldwork tracker disaggregated by state, LGA, respondent group and intervention approach; flag under-represented groups, contradictory cases and emerging gaps. Support approved transcription/translation coordination and transcript-to-audio or bilingual quality checks where assigned, without assuming responsibility for all study-wide transcription or analysis. Securely label, de-identify where appropriate, organize and transfer field notes, audio, consent records and other assigned materials through MC-approved systems; keep identifying records separate. Prepare a concise state-level completion report and outstanding-issues log; hand over all assigned records to the Lead Consultant and designated MC study personnel. Expected deliverables by staff cadre No. Cadre-specific deliverable Timing 1 Research Assistants: state workplan, stakeholder contacts and field schedule Within 2 working days of start 2 Research Assistants: approved recruitment and scheduling tracker; Moderators: session readiness/consent check Within 4 working days; updated as needed 3 Research Assistants: daily recruitment/session tracker; Moderators: completed FGD/KII session record; Note Takers: session metadata Daily during fieldwork 4 Research Assistants: state completion report; Moderators/Note Takers: session issue summaries; Transcribers: transcription status report Within 2 working days after state fieldwork 5 All cadres: final handover of assigned records and files, verified by Lead Consultant By last day of engagement Field Logistics and Responsibilities Item Responsibility/arrangement Participant identification/mobilization MC/state/LGA counterparts facilitate approved introductions; Research Assistants coordinate screening, recruitment and scheduling; Moderators verify eligibility/consent as assigned; Note Takers document session codes; Transcribers have no recruitment role. Venues MC/state teams support venue identification; Research Assistants coordinate booking and logistics; Moderators assess privacy and suitability; Note Takers prepare recording/notes materials. Participant transport reimbursement MC alone approves and administers reimbursement permitted by ethics documents; no Research Assistant, Moderator, Note Taker or Transcriber may introduce incentives or vary arrangements. Government/state/LGA introductions MC and government partners provide official introductions; Research Assistants coordinate field access under Lead Consultant direction. Access to quantitative/programme data for triangulation MC controls authorised programme data. Field cadres may access only the materials required for assigned tasks, through approved channels. Qualifications and Selection Criteria for Research Assistant Master’s degree in public health, epidemiology, social/behavioural sciences, implementation science, health services research or related discipline. At least three years of relevant qualitative public-health research or field coordination experience; experience with FGDs and KIIs, recruitment, note-taking and interviewing. Demonstrated understanding of informed consent, confidentiality, safeguarding, research data quality and secure file handling. Knowledge of SMC, routine immunisation, PHC or community health delivery is desirable. Proficiency in English and relevant local language(s) in the assigned state; strong communication and organisational skills. Resident in the state of assignment and available to travel to selected LGAs and work throughout the agreed period. Ethics, quality assurance and data protection All four cadres must comply with the approved protocol, ethics approvals, participant information sheets and consent forms. Research Assistants coordinate ethical recruitment and scheduling; Moderators verify and document consent, including separate audio-recording permission; Note Takers protect identities in field notes; and Transcribers process only authorised recordings and redact identifiers. Participation is voluntary and no field staff member may promise incentives. Any permitted transport reimbursement is determined and administered by MC. Every cadre must use approved study IDs, safeguard identifiable information, use authorised devices and secure transfer channels, and promptly report breaches, distress, deviations or missing records to the Lead Consultant and MC as appropriate. Recordings, notes and transcripts must be handed over securely, and local copies retained or deleted only as instructed by MC. Quality Assurance Requirements Only personnel demonstrating adequate competence during training/practical exercises will be deployed. All sessions must use the approved version of the relevant respondent-specific guide. Moderators and Note Takers must participate in post-session debriefs; Research Assistants maintain session QA and corrective-action logs; Transcribers must flag inaudible segments, inconsistencies and translation uncertainties. Transcribers will verify transcripts against audio and use agreed speaker codes; the Lead Consultant determines independent bilingual review and any subsequent analytical coding/double-coding. All four cadres document deviations and adaptations within their responsibilities; the Lead Consultant maintains the overall methodological and analysis audit trail. Each cadre submits its assigned editable field records, notes, audio metadata, transcripts, translations and discrepancy logs in approved formats. Codebooks, coding matrices and analytical projects remain the Lead Consultant’s responsibility. All editable datasets/files, transcripts, codebooks, matrices, coding outputs and analysis project files must be complete and submitted in agreed formats. Performance assessment and payment Performance and payment will be assessed separately for each cadre against its assigned duties: Research Assistantsrecruitment accuracy, schedules, trackers, QA and state handover; Moderatorsethical, complete and neutral FGDs/KIIs, probing and session documentation; Note Takersaccurate, timely field notes, metadata and debrief records; Transcriberscomplete, accurate, de-identified and timely transcripts/approved translations. All cadres must comply with supervision, safeguarding and data-security requirements. Individual contracts will specify working days or output-based units, approved rates, acceptance criteria and payment milestones; no consultant-level analysis or final-report obligations apply. Data Ownership, Management, Transfer, Retention and Deletion Malaria Consortium is the Data Controller and retains ownership and control of all study data and outputs generated by every field cadre, subject to contracts and applicable law. Identifying administrative information must be stored separately from study data. Unique study IDs must be used on research data. Audio, transcripts, codebooks, matrices and analysis projects must be stored only on password-protected/encrypted devices and MC-approved secure storage locations, with access limited to authorised personnel. Research Assistants, Moderators and Note Takers must transfer approved field records securely; Transcribers must return transcripts and any approved translations through MC-approved channels. The Lead Consultant verifies completeness and coordinates final handover to MC. MC retains records according to organizational policy and applicable ethical/data-protection requirements; no field cadre may retain copies beyond the period expressly authorised by MC. After confirmed handover and on MC’s written instruction, each staff member must securely delete unauthorized local copies and confirm completion; no fixed deletion deadline is imposed here unless specified by MC. No data may be reused, published, shared or transferred to third parties without prior written authorisation from MC and any required ethics/data-governance approval. Reporting and Management Arrangements All four cadres report technically to the Lead Qualitative Research Consultant. Research Assistants serve as state-level coordination focal points; Moderators and Note Takers coordinate session arrangements with the Research Assistants and report technical/session issues directly to the Lead Consultant; Transcribers receive authorised recordings and submit transcripts through the agreed secure workflow. MC retains overall oversight and approval authority. Each staff member must communicate progress, delays, data-quality issues and safeguarding/security concerns promptly.

2 hours ago

Note Taker

Malaria Consortium

Kogi, Nigeria

Full-time

Malaria Consortium (MC) is implementing an embedded implementation research study in selected local government areas (LGAs) of Kogi, Plateau and Sokoto States to assess approaches for linking routine immunization (RI) activities with Seasonal Malaria Chemoprevention (SMC) delivery. The approaches comprise: A, structured RI messaging during SMC contact; B, Approach A plus community engagement/social and behaviour change communication (SBCC); and C, Approach B plus immunization-status screening, referral and follow-up. A comparator arm receives standard SMC. The qualitative component explores acceptability, feasibility, implementation burden, fidelity, perceived effectiveness, equity and scalability. MC seeks six state-based Research Assistants (RAs), two in each state, and other state-level data collection team members (Moderators, Notetakers and qualitative data transcribers) to support the approved qualitative fieldwork. The RAs will work under the day-to-day technical direction and supervision of the Lead Qualitative Research Consultant and within MC-approved study procedures. We are recruiting to fill the position below: Job Title: Note Taker Location: Ibaji, Olamaboro - Kogi Purpose and limits of the Assignment Note Takers to undertake approved state-level qualitative fieldwork. Note Takers document sessions and support debriefs; and Transcribers produce accurate, de-identified transcripts and approved translations. Note Takers will work under the technical supervision of the This ToR covers field personnel only. No cadre is engaged to independently design or amend the protocol, approve sampling changes, lead the consultancy, undertake study-wide qualitative analysis, or prepare the final integrated research report. Duties are allocated by cadre and may overlap only when specifically assigned, personnel are trained and competent, and the Lead Consultant authorizes the arrangement. Locations (Applicants residing in these LGAs are encouraged to apply) Ibaji, Olamaboro - Kogi Qualitative Study Participants and Planned Sample The Lead Qualitative Research Consultant will operationalize the approved multi-stage sampling process with MC and government counterparts. State Research Assistants will implement the approved recruitment plan and coordinate scheduling; Moderators and Note Takers will support eligibility checks and consent within their training and assigned roles; Transcribers will work only with authorized, consented recordings. No field cadre may independently change the sampling frame or respondent targets. Participant Identification and Recruitment: The Research Assistants, based in Kogi, Plateau and Sokoto States, with the support of the moderators, Note takers and transcribers will coordinate participant identification and recruitment for qualitative data collection in their respective states, working closely with Malaria Consortium (MC), State Programme Managers and relevant state/LGA authorities to facilitate official introductions, access to selected clusters and model facilities, and participant mobilisation through appropriate community and programme structures. The Research Assistants with the support of the moderators, Note takers and transcribers will coordinate the implementation of the MC-approved sampling and recruitment plan, ensuring that approved recruitment lists and eligibility criteria are followed. They will oversee the screening process, maintain accurate screening and recruitment logs, monitor recruitment progress and support the selection of participants representing diverse roles, geographical locations and levels of intervention exposure. The Research Assistants will coordinate with trained qualitative data collectors to ensure that prospective participants are approached appropriately, eligibility is verified, and recruitment and informed consent procedures comply with the approved study protocol and ethical requirements. Recruitment and consent will be undertaken by trained research personnel who are not directly responsible for providing services to prospective participants to minimize potential coercion and power imbalances. The Research Assistants will coordinate the identification, recruitment and scheduling of the relevant respondent groups in their respective states, including caregivers and community drug distributors (CDDs) from the selected qualitative cluster in each intervention LGA; health workers from model facilities serving the selected clusters; community/traditional leaders in the three Approach C LGAs; and programme stakeholders purposively selected based on their responsibilities for SMC, routine immunization (RI), primary healthcare (PHC) planning, implementation, supervision or oversight. The Research Assistants will monitor recruitment against the approved state-level targets and data collection schedule, document recruitment challenges, ineligibility and non-response, and promptly communicate any proposed respondent replacements to the study lead and MC for review and approval. MC will retain final approval of the recruitment matrix and any replacement of a selected respondent. Supervision and working relationships: The Lead Qualitative Research Consultant provides direct technical supervision to all four field cadres, including orientation, daily task allocation, coaching, fieldwork review, transcription standards and approval of routine adjustments within the MC-approved plan. Research Assistants coordinate state-level scheduling and day-to-day communication, but do not replace the Lead Consultant as technical supervisor. Research Assistants submit consolidated state updates; Moderators submit session completion records and interview issues; Note Takers submit session notes and debrief records; and Transcribers submit transcripts and discrepancy logs. Each cadre must promptly report consent, safeguarding, confidentiality, security or quality concerns to the Lead Consultant, with escalation to MC under approved procedures. MC retains overall authority for protocol, ethics, safeguarding, data governance, participant reimbursement and material changes to sampling or field procedures. MC/state/LGA counterparts support official introductions, access and approved mobilisation. No cadre may independently substitute participants, alter approved reimbursement or disclose study data. RAs and other data collection team members do not independently approve protocol changes, substitute respondents, alter reimbursement arrangements or share research data outside authorised channels. Responsibilities of each Note taker The qualitative data collection notetaker will support the moderator by systematically documenting important verbal and non-verbal information during interviews and focus group discussions. The notetaker will: Record key points, significant statements, emerging issues, and contextual information during each session. Document relevant non-verbal observations, including participants' interactions, pauses, emotional reactions, gestures, group dynamics, and other behaviours that may contribute to interpretation of the data. Record the date, location, participant/session identification code, duration, and other relevant contextual details for each session. Avoid influencing the discussion or interrupting participants unnecessarily while taking notes. Where applicable, document the sequence of speakers or use participant codes to distinguish contributions during focus group discussions. Note issues requiring further probing or clarification by the moderator. Immediately after each session, review and complete the field notes in consultation with the moderator while the discussion remains fresh. Participate in post-session debriefings with the moderator to identify emerging themes, contextual observations, and potential gaps requiring attention in subsequent interviews. Maintain confidentiality and ensure that notes do not contain unnecessary personally identifying information. Securely store all field notes and transfer them to the designated research team member in accordance with the study's data management procedures. Report any technical, logistical, ethical, or participant-related issues encountered during data collection to the qualitative research supervisor. Expected deliverables by staff cadre No. Cadre-specific deliverable Timing 1 Moderators: session guide/consent/audio checklist; Note Takers: expanded field notes and debrief record; Research Assistants: daily QA log After each session / daily 2 Moderators/Note Takers: securely handed-over recordings and notes; Transcribers: verbatim transcripts, approved translations and discrepancy log; Research Assistants: handover tracker Rolling handover during fieldwork 3 All cadres: final handover of assigned records and files, verified by Lead Consultant By last day of engagement Field Logistics and Responsibilities Item Responsibility/arrangement Participant identification/mobilization MC/state/LGA counterparts facilitate approved introductions; Research Assistants coordinate screening, recruitment and scheduling; Moderators verify eligibility/consent as assigned; Note Takers document session codes; Transcribers have no recruitment role. Venues MC/state teams support venue identification; Research Assistants coordinate booking and logistics; Moderators assess privacy and suitability; Note Takers prepare recording/notes materials. Participant transport reimbursement MC alone approves and administers reimbursement permitted by ethics documents; no Research Assistant, Moderator, Note Taker or Transcriber may introduce incentives or vary arrangements. Government/state/LGA introductions MC and government partners provide official introductions; Research Assistants coordinate field access under Lead Consultant direction. Access to quantitative/programme data for triangulation MC controls authorised programme data. Field cadres may access only the materials required for assigned tasks, through approved channels. Qualifications and Selection Criteria for Note taker Bachelor’s Degree or equivalent qualification in Public Health, Social Sciences, Behavioural Sciences, Sociology, Anthropology, Psychology, or a related discipline. At least one year of experience supporting qualitative research, including FGDs, KIIs, interviews, or field data collection. Demonstrated ability to take accurate, organized, and timely field notes, including key statements, contextual information, and relevant non-verbal observations. Good understanding of research ethics, informed consent, confidentiality, and secure handling of research data. Good communication, listening, observation, and organizational skills. Proficiency in English and relevant local language(s) spoken in the assigned state. Knowledge of SMC, routine immunization, primary health care, or community health programmes is desirable. Resident in the LGA of assignment and available to travel to selected study sites during the agreed data collection period. Ethics, quality assurance and data protection: All four cadres must comply with the approved protocol, ethics approvals, participant information sheets and consent forms. Research Assistants coordinate ethical recruitment and scheduling; Moderators verify and document consent, including separate audio-recording permission; Note Takers protect identities in field notes; and Transcribers process only authorised recordings and redact identifiers. Participation is voluntary and no field staff member may promise incentives. Any permitted transport reimbursement is determined and administered by MC. Every cadre must use approved study IDs, safeguard identifiable information, use authorised devices and secure transfer channels, and promptly report breaches, distress, deviations or missing records to the Lead Consultant and MC as appropriate. Recordings, notes and transcripts must be handed over securely, and local copies retained or deleted only as instructed by MC. Quality Assurance Requirements: Only personnel demonstrating adequate competence during training/practical exercises will be deployed. All sessions must use the approved version of the relevant respondent-specific guide. Moderators and Note Takers must participate in post-session debriefs; Research Assistants maintain session QA and corrective-action logs; Transcribers must flag inaudible segments, inconsistencies and translation uncertainties. Transcribers will verify transcripts against audio and use agreed speaker codes; the Lead Consultant determines independent bilingual review and any subsequent analytical coding/double-coding. All four cadres document deviations and adaptations within their responsibilities; the Lead Consultant maintains the overall methodological and analysis audit trail. Each cadre submits its assigned editable field records, notes, audio metadata, transcripts, translations and discrepancy logs in approved formats. Codebooks, coding matrices and analytical projects remain the Lead Consultant’s responsibility. All editable datasets/files, transcripts, codebooks, matrices, coding outputs and analysis project files must be complete and submitted in agreed formats. Performance assessment and payment: Performance and payment will be assessed separately for each cadre against its assigned duties: Research Assistantsrecruitment accuracy, schedules, trackers, QA and state handover; Moderatorsethical, complete and neutral FGDs/KIIs, probing and session documentation; Note Takersaccurate, timely field notes, metadata and debrief records; Transcriberscomplete, accurate, de-identified and timely transcripts/approved translations. All cadres must comply with supervision, safeguarding and data-security requirements. Individual contracts will specify working days or output-based units, approved rates, acceptance criteria and payment milestones; no consultant-level analysis or final-report obligations apply. Data Ownership, Management, Transfer, Retention and Deletion: Malaria Consortium is the Data Controller and retains ownership and control of all study data and outputs generated by every field cadre, subject to contracts and applicable law. Identifying administrative information must be stored separately from study data. Unique study IDs must be used on research data. Audio, transcripts, codebooks, matrices and analysis projects must be stored only on password-protected/encrypted devices and MC-approved secure storage locations, with access limited to authorized personnel. Research Assistants, Moderators and Note Takers must transfer approved field records securely; Transcribers must return transcripts and any approved translations through MC-approved channels. The Lead Consultant verifies completeness and coordinates final handover to MC. MC retains records according to organizational policy and applicable ethical/data-protection requirements; no field cadre may retain copies beyond the period expressly authorized by MC. After confirmed handover and on MC’s written instruction, each staff member must securely delete unauthorized local copies and confirm completion; no fixed deletion deadline is imposed here unless specified by MC. No data may be reused, published, shared or transferred to third parties without prior written authorization from MC and any required ethics/data-governance approval. Reporting and Management Arrangements: All four cadres report technically to the Lead Qualitative Research Consultant. Research Assistants serve as state-level coordination focal points; Moderators and Note Takers coordinate session arrangements with the Research Assistants and report technical/session issues directly to the Lead Consultant; Transcribers receive authorized recordings and submit transcripts through the agreed secure workflow. MC retains overall oversight and approval authority. Each staff member must communicate progress, delays, data-quality issues and safeguarding/security concerns promptly.

2 hours ago

Data Transcriber (plateau)

Malaria Consortium

Plateau, Nigeria

Full-time

Malaria Consortium (MC) is implementing an embedded implementation research study in selected local government areas (LGAs) of Kogi, Plateau and Sokoto States to assess approaches for linking routine immunization (RI) activities with Seasonal Malaria Chemoprevention (SMC) delivery. The approaches comprise: A, structured RI messaging during SMC contact; B, Approach A plus community engagement/social and behaviour change communication (SBCC); and C, Approach B plus immunization-status screening, referral and follow-up. A comparator arm receives standard SMC. The qualitative component explores acceptability, feasibility, implementation burden, fidelity, perceived effectiveness, equity and scalability. MC seeks six state-based Research Assistants (RAs), two in each state, and other state-level data collection team members (Moderators, Notetakers and qualitative data transcribers) to support the approved qualitative fieldwork. The RAs will work under the day-to-day technical direction and supervision of the Lead Qualitative Research Consultant and within MC-approved study procedures. We are recruiting to fill the position below: Job Title: Data Transcriber Location: Plateau Purpose and limits of the assignment To undertake approved state-level qualitative fieldwork. Transcribers produce accurate, de-identified transcripts and approved translations. All cadres work under the technical supervision of the Lead Qualitative Research Consultant and Malaria Consortium (MC) oversight. This ToR covers field personnel only. No cadre is engaged to independently design or amend the protocol, approve sampling changes, lead the consultancy, undertake study-wide qualitative analysis, or prepare the final integrated research report. Duties are allocated by cadre and may overlap only when specifically assigned, personnel are trained and competent, and the Lead Consultant authorizes the arrangement. Qualitative Study Participants and Planned Sample The Lead Qualitative Research Consultant will operationalize the approved multi-stage sampling process with MC and government counterparts. State Research Assistants will implement the approved recruitment plan and coordinate scheduling; Moderators and Note Takers will support eligibility checks and consent within their training and assigned roles; Transcribers will work only with authorized, consented recordings. No field cadre may independently change the sampling frame or respondent targets. Participant Identification and Recruitment The Research Assistants, based in Kogi, Plateau and Sokoto States, with the support of the moderators, Note takers and transcribers will coordinate participant identification and recruitment for qualitative data collection in their respective states, working closely with Malaria Consortium (MC), State Programme Managers and relevant state/LGA authorities to facilitate official introductions, access to selected clusters and model facilities, and participant mobilisation through appropriate community and programme structures. The Research Assistants with the support of the moderators, Note takers and transcribers will coordinate the implementation of the MC-approved sampling and recruitment plan, ensuring that approved recruitment lists and eligibility criteria are followed. They will oversee the screening process, maintain accurate screening and recruitment logs, monitor recruitment progress and support the selection of participants representing diverse roles, geographical locations and levels of intervention exposure. The Research Assistants will coordinate with trained qualitative data collectors to ensure that prospective participants are approached appropriately, eligibility is verified, and recruitment and informed consent procedures comply with the approved study protocol and ethical requirements. Recruitment and consent will be undertaken by trained research personnel who are not directly responsible for providing services to prospective participants to minimize potential coercion and power imbalances. The Research Assistants will coordinate the identification, recruitment and scheduling of the relevant respondent groups in their respective states, including caregivers and community drug distributors (CDDs) from the selected qualitative cluster in each intervention LGA; health workers from model facilities serving the selected clusters; community/traditional leaders in the three Approach C LGAs; and programme stakeholders purposively selected based on their responsibilities for SMC, routine immunization (RI), primary healthcare (PHC) planning, implementation, supervision or oversight. The Research Assistants will monitor recruitment against the approved state-level targets and data collection schedule, document recruitment challenges, ineligibility and non-response, and promptly communicate any proposed respondent replacements to the study lead and MC for review and approval. MC will retain final approval of the recruitment matrix and any replacement of a selected respondent. Supervision and working relationships: The Lead Qualitative Research Consultant provides direct technical supervision to all four field cadres, including orientation, daily task allocation, coaching, fieldwork review, transcription standards and approval of routine adjustments within the MC-approved plan. Research Assistants coordinate state-level scheduling and day-to-day communication, but do not replace the Lead Consultant as technical supervisor. Research Assistants submit consolidated state updates; Moderators submit session completion records and interview issues; Note Takers submit session notes and debrief records; and Transcribers submit transcripts and discrepancy logs. Each cadre must promptly report consent, safeguarding, confidentiality, security or quality concerns to the Lead Consultant, with escalation to MC under approved procedures. MC retains overall authority for protocol, ethics, safeguarding, data governance, participant reimbursement and material changes to sampling or field procedures. MC/state/LGA counterparts support official introductions, access and approved mobilisation. No cadre may independently substitute participants, alter approved reimbursement or disclose study data. RAs and other data collection team members do not independently approve protocol changes, substitute respondents, alter reimbursement arrangements or share research data outside authorised channels. Responsibilities of each Transcriber The qualitative data transcriber will be responsible for producing accurate and complete transcripts of recorded interviews and focus group discussions while maintaining confidentiality and data security. The transcriber will: Transcribe audio recordings verbatim and accurately, according to the study's approved transcription procedures. Preserve the meaning, context, and sequence of participants' responses without intentionally altering or interpreting their statements. Clearly distinguish between the moderator/interviewer and individual participants using approved participant or speaker identification codes. Include relevant non-verbal expressions or contextual information that are important for interpretation, where identifiable from the recording. Ensure that transcripts are complete and correspond to the correct audio recording and session identification code. Where required, translate interviews conducted in local languages into English while maintaining the original meaning and context of participants' responses. Flag sections of the recording that are inaudible, unclear, or difficult to interpret rather than guessing or fabricating content. Remove or replace personally identifying information with appropriate identifiers or anonymised codes in accordance with the study's confidentiality procedures. Maintain strict confidentiality regarding the content of interviews and focus group discussions. Store audio recordings and transcripts securely and access them only for authorised study purposes. Review completed transcripts against the original audio recording to identify and correct transcription errors. Report technical problems, missing recordings, poor audio quality, or other issues affecting transcription to the qualitative research supervisor. Submit completed transcripts within the agreed timeframe and in the required format for quality assurance, coding, and analysis. Not retain, share, reproduce, or disclose study recordings or transcripts outside the authorised research team. Expected deliverables by staff cadre No. Cadre-specific deliverable Timing 1 Moderators/Note Takers: securely handed-over recordings and notes; Transcribers: verbatim transcripts, approved translations and discrepancy log; Research Assistants: handover tracker Rolling handover during fieldwork 2 Research Assistants: state completion report; Moderators/Note Takers: session issue summaries; Transcribers: transcription status report Within 2 working days after state fieldwork 3 All cadres: final handover of assigned records and files, verified by Lead Consultant By last day of engagement Field Logistics and Responsibilities Item Responsibility/arrangement Participant identification/mobilization MC/state/LGA counterparts facilitate approved introductions; Research Assistants coordinate screening, recruitment and scheduling; Moderators verify eligibility/consent as assigned; Note Takers document session codes; Transcribers have no recruitment role. Venues MC/state teams support venue identification; Research Assistants coordinate booking and logistics; Moderators assess privacy and suitability; Note Takers prepare recording/notes materials. Participant transport reimbursement MC alone approves and administers reimbursement permitted by ethics documents; no Research Assistant, Moderator, Note Taker or Transcriber may introduce incentives or vary arrangements. Government/state/LGA introductions MC and government partners provide official introductions; Research Assistants coordinate field access under Lead Consultant direction. Access to quantitative/programme data for triangulation MC controls authorised programme data. Field cadres may access only the materials required for assigned tasks, through approved channels. Qualifications and Selection Criteria for Transcriber Bachelor’s degree or equivalent qualification in Linguistics, English, Communication, Social Sciences, Public Health, or a related discipline. At least one year of experience transcribing qualitative interviews, Focus Group Discussions (FGDs), or Key Informant Interviews (KIIs). Demonstrated ability to produce accurate, complete, and well-organised verbatim transcripts while preserving the meaning and context of participants’ responses. Proficiency in English and relevant local language(s), with the ability to transcribe and, where required, translate recordings accurately. Good listening, typing, attention-to-detail, and time-management skills, with proficiency in word-processing software. Understanding of research ethics, confidentiality, anonymisation, and secure handling of audio recordings and transcripts. Available throughout the agreed transcription period and able to meet established deadlines. Ethics, quality assurance and data protection All four cadres must comply with the approved protocol, ethics approvals, participant information sheets and consent forms. Research Assistants coordinate ethical recruitment and scheduling; Moderators verify and document consent, including separate audio-recording permission; Note Takers protect identities in field notes; and Transcribers process only authorised recordings and redact identifiers. Participation is voluntary and no field staff member may promise incentives. Any permitted transport reimbursement is determined and administered by MC. Every cadre must use approved study IDs, safeguard identifiable information, use authorised devices and secure transfer channels, and promptly report breaches, distress, deviations or missing records to the Lead Consultant and MC as appropriate. Recordings, notes and transcripts must be handed over securely, and local copies retained or deleted only as instructed by MC. Quality Assurance Requirements Only personnel demonstrating adequate competence during training/practical exercises will be deployed. All sessions must use the approved version of the relevant respondent-specific guide. Moderators and Note Takers must participate in post-session debriefs; Research Assistants maintain session QA and corrective-action logs; Transcribers must flag inaudible segments, inconsistencies and translation uncertainties. Transcribers will verify transcripts against audio and use agreed speaker codes; the Lead Consultant determines independent bilingual review and any subsequent analytical coding/double-coding. All four cadres document deviations and adaptations within their responsibilities; the Lead Consultant maintains the overall methodological and analysis audit trail. Each cadre submits its assigned editable field records, notes, audio metadata, transcripts, translations and discrepancy logs in approved formats. Codebooks, coding matrices and analytical projects remain the Lead Consultant’s responsibility. All editable datasets/files, transcripts, codebooks, matrices, coding outputs and analysis project files must be complete and submitted in agreed formats. Performance assessment and payment Performance and payment will be assessed separately for each cadre against its assigned duties: Research Assistantsrecruitment accuracy, schedules, trackers, QA and state handover; Moderatorsethical, complete and neutral FGDs/KIIs, probing and session documentation; Note Takersaccurate, timely field notes, metadata and debrief records; Transcriberscomplete, accurate, de-identified and timely transcripts/approved translations. All cadres must comply with supervision, safeguarding and data-security requirements. Individual contracts will specify working days or output-based units, approved rates, acceptance criteria and payment milestones; no consultant-level analysis or final-report obligations apply. Data Ownership, Management, Transfer, Retention and Deletion Malaria Consortium is the Data Controller and retains ownership and control of all study data and outputs generated by every field cadre, subject to contracts and applicable law. Identifying administrative information must be stored separately from study data. Unique study IDs must be used on research data. Audio, transcripts, codebooks, matrices and analysis projects must be stored only on password-protected/encrypted devices and MC-approved secure storage locations, with access limited to authorised personnel. Research Assistants, Moderators and Note Takers must transfer approved field records securely; Transcribers must return transcripts and any approved translations through MC-approved channels. The Lead Consultant verifies completeness and coordinates final handover to MC. MC retains records according to organisational policy and applicable ethical/data-protection requirements; no field cadre may retain copies beyond the period expressly authorised by MC. After confirmed handover and on MC’s written instruction, each staff member must securely delete unauthorised local copies and confirm completion; no fixed deletion deadline is imposed here unless specified by MC. No data may be reused, published, shared or transferred to third parties without prior written authorization from MC and any required ethics/data-governance approval. Reporting and Management Arrangements Transcribers receive authorised recordings and submit transcripts through the agreed secure workflow. MC retains overall oversight and approval authority. Each staff member must communicate progress, delays, data-quality issues and safeguarding/security concerns promptly.

2 hours ago

Data Transcriber

Malaria Consortium

Sokoto, Nigeria

Full-time

Malaria Consortium (MC) is implementing an embedded implementation research study in selected local government areas (LGAs) of Kogi, Plateau and Sokoto States to assess approaches for linking routine immunization (RI) activities with Seasonal Malaria Chemoprevention (SMC) delivery. The approaches comprise: A, structured RI messaging during SMC contact; B, Approach A plus community engagement/social and behaviour change communication (SBCC); and C, Approach B plus immunization-status screening, referral and follow-up. A comparator arm receives standard SMC. The qualitative component explores acceptability, feasibility, implementation burden, fidelity, perceived effectiveness, equity and scalability. MC seeks six state-based Research Assistants (RAs), two in each state, and other state-level data collection team members (Moderators, Notetakers and qualitative data transcribers) to support the approved qualitative fieldwork. The RAs will work under the day-to-day technical direction and supervision of the Lead Qualitative Research Consultant and within MC-approved study procedures. We are recruiting to fill the position below: Job Title: Data Transcriber Location: Silame, Shagari, Binji - Sokoto Employment Type: Purpose and limits of the assignment To undertake approved state-level qualitative fieldwork. Transcribers produce accurate, de-identified transcripts and approved translations. All cadres work under the technical supervision of the Lead Qualitative Research Consultant and Malaria Consortium (MC) oversight. This ToR covers field personnel only. No cadre is engaged to independently design or amend the protocol, approve sampling changes, lead the consultancy, undertake study-wide qualitative analysis, or prepare the final integrated research report. Duties are allocated by cadre and may overlap only when specifically assigned, personnel are trained and competent, and the Lead Consultant authorizes the arrangement. Qualitative Study Participants and Planned Sample The Lead Qualitative Research Consultant will operationalize the approved multi-stage sampling process with MC and government counterparts. State Research Assistants will implement the approved recruitment plan and coordinate scheduling; Moderators and Note Takers will support eligibility checks and consent within their training and assigned roles; Transcribers will work only with authorized, consented recordings. No field cadre may independently change the sampling frame or respondent targets. Participant Identification and Recruitment The Research Assistants, based in Kogi, Plateau and Sokoto States, with the support of the moderators, Note takers and transcribers will coordinate participant identification and recruitment for qualitative data collection in their respective states, working closely with Malaria Consortium (MC), State Programme Managers and relevant state/LGA authorities to facilitate official introductions, access to selected clusters and model facilities, and participant mobilisation through appropriate community and programme structures. The Research Assistants with the support of the moderators, Note takers and transcribers will coordinate the implementation of the MC-approved sampling and recruitment plan, ensuring that approved recruitment lists and eligibility criteria are followed. They will oversee the screening process, maintain accurate screening and recruitment logs, monitor recruitment progress and support the selection of participants representing diverse roles, geographical locations and levels of intervention exposure. The Research Assistants will coordinate with trained qualitative data collectors to ensure that prospective participants are approached appropriately, eligibility is verified, and recruitment and informed consent procedures comply with the approved study protocol and ethical requirements. Recruitment and consent will be undertaken by trained research personnel who are not directly responsible for providing services to prospective participants to minimize potential coercion and power imbalances. The Research Assistants will coordinate the identification, recruitment and scheduling of the relevant respondent groups in their respective states, including caregivers and community drug distributors (CDDs) from the selected qualitative cluster in each intervention LGA; health workers from model facilities serving the selected clusters; community/traditional leaders in the three Approach C LGAs; and programme stakeholders purposively selected based on their responsibilities for SMC, routine immunization (RI), primary healthcare (PHC) planning, implementation, supervision or oversight. The Research Assistants will monitor recruitment against the approved state-level targets and data collection schedule, document recruitment challenges, ineligibility and non-response, and promptly communicate any proposed respondent replacements to the study lead and MC for review and approval. MC will retain final approval of the recruitment matrix and any replacement of a selected respondent. Supervision and working relationships: The Lead Qualitative Research Consultant provides direct technical supervision to all four field cadres, including orientation, daily task allocation, coaching, fieldwork review, transcription standards and approval of routine adjustments within the MC-approved plan. Research Assistants coordinate state-level scheduling and day-to-day communication, but do not replace the Lead Consultant as technical supervisor. Research Assistants submit consolidated state updates; Moderators submit session completion records and interview issues; Note Takers submit session notes and debrief records; and Transcribers submit transcripts and discrepancy logs. Each cadre must promptly report consent, safeguarding, confidentiality, security or quality concerns to the Lead Consultant, with escalation to MC under approved procedures. MC retains overall authority for protocol, ethics, safeguarding, data governance, participant reimbursement and material changes to sampling or field procedures. MC/state/LGA counterparts support official introductions, access and approved mobilisation. No cadre may independently substitute participants, alter approved reimbursement or disclose study data. RAs and other data collection team members do not independently approve protocol changes, substitute respondents, alter reimbursement arrangements or share research data outside authorised channels. Responsibilities of each Transcriber The qualitative data transcriber will be responsible for producing accurate and complete transcripts of recorded interviews and focus group discussions while maintaining confidentiality and data security. The transcriber will: Transcribe audio recordings verbatim and accurately, according to the study's approved transcription procedures. Preserve the meaning, context, and sequence of participants' responses without intentionally altering or interpreting their statements. Clearly distinguish between the moderator/interviewer and individual participants using approved participant or speaker identification codes. Include relevant non-verbal expressions or contextual information that are important for interpretation, where identifiable from the recording. Ensure that transcripts are complete and correspond to the correct audio recording and session identification code. Where required, translate interviews conducted in local languages into English while maintaining the original meaning and context of participants' responses. Flag sections of the recording that are inaudible, unclear, or difficult to interpret rather than guessing or fabricating content. Remove or replace personally identifying information with appropriate identifiers or anonymised codes in accordance with the study's confidentiality procedures. Maintain strict confidentiality regarding the content of interviews and focus group discussions. Store audio recordings and transcripts securely and access them only for authorised study purposes. Review completed transcripts against the original audio recording to identify and correct transcription errors. Report technical problems, missing recordings, poor audio quality, or other issues affecting transcription to the qualitative research supervisor. Submit completed transcripts within the agreed timeframe and in the required format for quality assurance, coding, and analysis. Not retain, share, reproduce, or disclose study recordings or transcripts outside the authorised research team. Expected deliverables by staff cadre No. Cadre-specific deliverable Timing 1 Moderators/Note Takers: securely handed-over recordings and notes; Transcribers: verbatim transcripts, approved translations and discrepancy log; Research Assistants: handover tracker Rolling handover during fieldwork 2 Research Assistants: state completion report; Moderators/Note Takers: session issue summaries; Transcribers: transcription status report Within 2 working days after state fieldwork 3 All cadres: final handover of assigned records and files, verified by Lead Consultant By last day of engagement Field Logistics and Responsibilities Item Responsibility/arrangement Participant identification/mobilization MC/state/LGA counterparts facilitate approved introductions; Research Assistants coordinate screening, recruitment and scheduling; Moderators verify eligibility/consent as assigned; Note Takers document session codes; Transcribers have no recruitment role. Venues MC/state teams support venue identification; Research Assistants coordinate booking and logistics; Moderators assess privacy and suitability; Note Takers prepare recording/notes materials. Participant transport reimbursement MC alone approves and administers reimbursement permitted by ethics documents; no Research Assistant, Moderator, Note Taker or Transcriber may introduce incentives or vary arrangements. Government/state/LGA introductions MC and government partners provide official introductions; Research Assistants coordinate field access under Lead Consultant direction. Access to quantitative/programme data for triangulation MC controls authorised programme data. Field cadres may access only the materials required for assigned tasks, through approved channels. Qualifications and Selection Criteria for Transcriber Bachelor’s degree or equivalent qualification in Linguistics, English, Communication, Social Sciences, Public Health, or a related discipline. At least one year of experience transcribing qualitative interviews, Focus Group Discussions (FGDs), or Key Informant Interviews (KIIs). Demonstrated ability to produce accurate, complete, and well-organised verbatim transcripts while preserving the meaning and context of participants’ responses. Proficiency in English and relevant local language(s), with the ability to transcribe and, where required, translate recordings accurately. Good listening, typing, attention-to-detail, and time-management skills, with proficiency in word-processing software. Understanding of research ethics, confidentiality, anonymisation, and secure handling of audio recordings and transcripts. Available throughout the agreed transcription period and able to meet established deadlines. Ethics, quality assurance and data protection: All four cadres must comply with the approved protocol, ethics approvals, participant information sheets and consent forms. Research Assistants coordinate ethical recruitment and scheduling; Moderators verify and document consent, including separate audio-recording permission; Note Takers protect identities in field notes; and Transcribers process only authorised recordings and redact identifiers. Participation is voluntary and no field staff member may promise incentives. Any permitted transport reimbursement is determined and administered by MC. Every cadre must use approved study IDs, safeguard identifiable information, use authorised devices and secure transfer channels, and promptly report breaches, distress, deviations or missing records to the Lead Consultant and MC as appropriate. Recordings, notes and transcripts must be handed over securely, and local copies retained or deleted only as instructed by MC. Quality Assurance Requirements: Only personnel demonstrating adequate competence during training/practical exercises will be deployed. All sessions must use the approved version of the relevant respondent-specific guide. Moderators and Note Takers must participate in post-session debriefs; Research Assistants maintain session QA and corrective-action logs; Transcribers must flag inaudible segments, inconsistencies and translation uncertainties. Transcribers will verify transcripts against audio and use agreed speaker codes; the Lead Consultant determines independent bilingual review and any subsequent analytical coding/double-coding. All four cadres document deviations and adaptations within their responsibilities; the Lead Consultant maintains the overall methodological and analysis audit trail. Each cadre submits its assigned editable field records, notes, audio metadata, transcripts, translations and discrepancy logs in approved formats. Codebooks, coding matrices and analytical projects remain the Lead Consultant’s responsibility. All editable datasets/files, transcripts, codebooks, matrices, coding outputs and analysis project files must be complete and submitted in agreed formats. Performance assessment and payment: Performance and payment will be assessed separately for each cadre against its assigned duties Transcribers to complete, accurate, de-identified and timely transcripts/approved translations. All cadres must comply with supervision, safeguarding and data-security requirements. Individual contracts will specify working days or output-based units, approved rates, acceptance criteria and payment milestones; no consultant-level analysis or final-report obligations apply. Data Ownership, Management, Transfer, Retention and Deletion: Malaria Consortium is the Data Controller and retains ownership and control of all study data and outputs generated by every field cadre, subject to contracts and applicable law. Identifying administrative information must be stored separately from study data. Unique study IDs must be used on research data. Audio, transcripts, codebooks, matrices and analysis projects must be stored only on password-protected/encrypted devices and MC-approved secure storage locations, with access limited to authorised personnel. Research Assistants, Moderators and Note Takers must transfer approved field records securely; Transcribers must return transcripts and any approved translations through MC-approved channels. The Lead Consultant verifies completeness and coordinates final handover to MC. MC retains records according to organisational policy and applicable ethical/data-protection requirements; no field cadre may retain copies beyond the period expressly authorised by MC. After confirmed handover and on MC’s written instruction, each staff member must securely delete unauthorised local copies and confirm completion; no fixed deletion deadline is imposed here unless specified by MC. No data may be reused, published, shared or transferred to third parties without prior written authorization from MC and any required ethics/data-governance approval. Reporting and Management Arrangements: Transcribers receive authorised recordings and submit transcripts through the agreed secure workflow. MC retains overall oversight and approval authority. Each staff member must communicate progress, delays, data-quality issues and safeguarding/security concerns promptly.

2 hours ago

Head Of Community

247Bet

Lagos, nigeria

full-time

Role Description This is a full-time hybrid role for a Head of Community, based in Lagos. Community is at the heart of what we're building, our platform consolidates a fragmented social betting ecosystem of tipsters, copy-betting, and PvP communities into one place. The Head of Community will own the strategy, growth, and health of our user community across in-app social features and external channels. You'll turn casual users into engaged, loyal members, build and lead a community team, and act as the voice of our users inside the company. This is a high-impact leadership role for someone who understands online communities deeply and can balance growth, engagement, and responsible gaming. What You'll Do Own and execute the end-to-end community strategy across in-app social features, tipster communities, and external channels (Telegram, WhatsApp, Discord, X, Instagram, TikTok) Grow an engaged, active community and drive retention, loyalty, and word-of-mouth referral Build, lead, and scale a team of community managers and moderators Define and track community health metrics engagement, sentiment, growth, and retention Design and run community programmes: tipster onboarding, ambassadors, events, competitions, and rewards Establish and enforce community guidelines and moderation standards, protecting users and upholding responsible gaming Act as the voice of the community internally, surfacing user feedback to product, marketing, and leadership Partner with marketing and product to launch features and campaigns that deepen community engagement Manage influencer and tipster relationships that anchor the social experience What We're Looking For 6+ years of experience in community management, social media, or growth, with time spent leading a team A track record of building and scaling an engaged online community at meaningful scale Deep understanding of Nigerian social platforms and online culture, especially around sports and betting Strong leadership skills and experience hiring, managing, and developing a team Data-driven approach to community growth, engagement, and retention Excellent written and verbal communication, with the ability to shape brand voice and tone A genuine instinct for what makes communities thrive, and a commitment to responsible gaming Nice to Have Experience in sports betting, gaming, fintech, or another high-engagement consumer product Familiarity with copy-betting, tipster, or creator-led community models Experience with community and social tooling (e.g. Discord, Telegram bots, social listening, CRM) Existing network within the Nigerian sports, betting, or creator ecosystem

2 months ago

Recruiters

BBC Media Action

Jigawa , Sokoto, nigeria

full-time

Key Responsibilities: Use the provided screener to identify and recruit participants who meet study criteria. Ensure participant quotas (e.g., gender, age, location, etc.) are met. Contact, brief, and confirm participants ahead of scheduled sessions. Maintain accurate recruitment records and participant contact details. Coordinate with moderators and supervisors to ensure participant attendance. Uphold confidentiality and ethical standards throughout the recruitment process.

2 months ago

Moderator

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