HR Graduate Programme

Key Responsibilities

• Assist with protocol development and associated plans and materials
• Provide assistance with development of study protocols, SOPs, ethics guidelines
• Assist with project monitoring
• Anticipate project issues and develop resolution strategies
• Work with team members on laboratory setup
• Provide administrative assistance including funding applications, ethics applications, abstracts and manuscripts
• Identify, evaluate and recruit research participants
• Organize research data and provide reports
• Analyze computerized physiological data
• Prepare reports for individual participants
• Liaise with clinical staff for patient follow-up
• Coordinate research tasks with other staff
• Train students on data entry and patient interactions
• Maintain up-to-date study documents
• Organize daily study activities, monitor timelines, schedule appointments
• Track patient-centered outcomes and assist with data analysis
• Implement efficiency and quality improvement ideas
• Manage data flows and generate queries

Requirements

Education

Master's degree in health or related discipline

Experience

Minimum of two years clinical trial experience

Required Skills

• Project coordination
• Patient interaction
• Multiple project management
• Interpersonal communication
• Team building
• MS Office proficiency
• R-Studio experience

Benefits

• Comprehensive benefits package