Clinical Research Co-ordinator

Responsibilities

• Coordinate and assist in the conduct of clinical research studies and trials in IMH in compliance with study protocols, applicable laws and regulations, principles, guidelines, policies and procedures.
• Conducts or assists in the monitoring and audit of research projects as required by institutional policies, ethics and regulatory requirements
• Supports and guides researchers on institutional policies, ethics and regulatory requirements for research conduct 
• Develops, reviews and implements research-related policies and processes
• Conduct relevant research training or education on proper of conduct of research.

Requirements

• Bachelor’s degree in health sciences studies or related disciplines
• Prior experience in research quality management, knowledge of research governance and ethics is preferred
• Good written and verbal communication skills, meticulous and able to multi-task
• Ability to work independently to meet deadlines
• Ability to draw blood will be an added advantage