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