Requirements
• Good understanding of research regulatory procedures
• A minimum of 2 years work experience, preferably in a research environment
• Good organizational skills
• Attention to detail
• Good oral and written communication skills
• Good presentations skills including MS, Excel and power point
• Demonstrated self-initiative and management skills
• Demonstrated problem-solving skills
• Demonstrated ability to build and maintain relationships with individuals and teams
• Willing to learn and complete tasks in time
• Coordinate research functions and develop capacity for Scientific Review of research proposals in line with National guidelines for Research Ethics Committees (RECs),
• Work closely with the National Drug Authority, for purposes of developing capacity for clinical trial monitoring
• Organize and facilitate project working group meetings and training sessions including writing minutes and report writing.
• Prepare and maintain program reports and summaries.
• Coordinate project-related training, networking events, and stakeholder engagement activities.
• Assist in development of stakeholder surveys, and trainee surveys.
• Support with protocol and manuscript writing.
• Maintain and organize project documents.
• Manage logistical aspects of training sessions.
• Support other research office activities as requested