Key Responsibilities:
Plan, manage, and supervise the day-to-day operations of the study ;
Supervise the study teams (Research Assistants and Data Analyst) to ensure that the study is conducted according to the study protocol and GCP;
Oversee recruitment, retentions, and data collection activities ;
Travel to field sites to ensure the smooth running of study activities;
Develop and manage standard Operating Procedures (SOPs) for all study procedures
Maintain Study Master File
Prepare and submit study documents to ethics and regulatory committees, including protocol
Organise and lead in-person and Zoom meetings regarding research updates, result.
Vacancy Requirements:
A Master’s Degree in Public Health, Nursing, Psychology, or Clinical Research Mandatory
Prior experience with at least one of the following: adolescents, STI/HIV prevention, school-based, and/or livelihood interventions Mandatory
Additional training in a management-related field and research ethics will be an added advantage Added Advantage
Experience with Clinical Trials Mandatory
Valid practicing license where applicable Mandatory
Excellent interpersonal skills Mandatory
High level of competency in using Microsoft, Excel, Word, and PowerPoint. Mandatory
Excellent organizational skills to independently manage workflow Mandatory
Excellent written and verbal communication skills Mandatory
Knowledge of sustainable agriculture practices. Mandatory
Experience in mentoring and supervising research staff. Mandatory
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