Position Objective:

• You will be responsible to support our client’s clinical trials by managing the clinical study requirements from study setup, through to day-to-day activities and study close out. The holder of this position is independent in carrying out assigned tasks listed below and expected to practice continuous improvement and self-training on our quality management system.

What will you do?

• Coordinating technical and service aspects of a given project, ensuring compliance with study requirements, ensure day to day operational study requirements are met
• Managing logistics for importation and delivery of investigational medicinal products
• Provide training to team members and stakeholders
• Participating in internal and external meetings
• Maintaining compliance with established procedures and standards
• Contributing to corporate goals
• Assisting in the investigation of non-conformances and customer complaints
• Liaising with global project managers or clients on drug returns and destruction requirements
• Timely provision of reports
• Design, implementation, maintenance and reporting of key performance indicators
• Continuous improvement and self-training on the quality management system
• Maintain the quality adherence through all processes
• Communication with clients and global project managers

How will you get here? Education

• Grade 12 or equivalent
• Project Management experience will be beneficial
• Any co-ordinational experience will be an advantage
• Excel intermediate level
• Clinical trial industry experience will be an advantage

Knowledge, Skills, Abilities:

• Effective time management and prioritization skills Self-driven and motivated
• Ability to work independently and be self-motivated with a positive attitude
• Collaborate cross departmental and cross organizational
• Customer focused
• Detailed orientated
• Financially orientated
• Ability to work under pressure and meet tight deadlines
• Strong excel capabilities