Job Description
Job Requirements/Responsibilities:
1. Sensitization of districts, refugee camps, and local stakeholders about the study.
2. Oversee protocol implementation and ensure compliance with GCP and ethical guidelines.
3. Maintain study documentation, including CRFs, consent forms, and regulatory binders.
4. Liaise with investigators, data managers, and ethics committees.
5. Planning and budgeting for field activities.
6. Participation in the development and training of protocol, SOPs, and data collection tools.
7. Conducting data quality assessments, mentorship, and CMEs for the study team.
8. Presentation of updates and reports to the MoH technical working groups.
9. Ensuring proper administration of informed consent, and proper collection and management of data.
10. Prepare and distribute study updates and reports.
11. Lead study team meetings.
12. Maintain confidentiality of records and research findings as appropriate.
13. Supervise the study field teams to ensure compliance.
14. Participate in data analysis, manuscript preparation, and dissemination of study findings.
Qualifications:
MASTERS : Medical graduate (MBChB/MD/BVM)with master’s dregree in Epidemiology/Biostatistics from a recongnized institution – Mandatory
: At least 2 years’ experience in a research environment. – Optional
Certifications:
Must have valid GCP and HSP certificates – Mandatory
Skill & Experience:
Excellent interpersonal skills/Experience working with and leading teams. – Mandatory
Proficiency in using statistical analysis softwares (STATA and R packages) – Mandatory
Must have good computer skills and reputable knowledge of Microsoft office packages. – Mandatory
Strong skills in developing work plans, setting timelines, and tracking project progress. – Mandatory
Exceptional organizational abilities to manage multiple projects and stakeholders efficiently. – Mandatory
Proficiency in database management systems – Optional
Excellent communication skills for report writing – Optional
Languages: