WHAT WE ARE LOOKING FOR

The successful candidate must be organised, highly self-motivated and have excellent communication, interpersonal and computer skills. They will need to manage their time and performance, must be strongly proactive, knowledgeable, and be able to solve complex problems. We are looking for someone willing to work within a team.

AVAILABLE DOCUMENTS

Attached documents are available under links. Clicking a document link will initialize its download.
Please note that job descriptions are not exhaustive, and you may be asked to take on additional duties that align with the key responsibilities mentioned above.
We reserve the right to close the advert prior to the closing date stated should we receive a high volume of applications. It is therefore advisable that you submit your application as early as possible to avoid disappointment.
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ABOUT THE ROLE

This position represents an opportunity for a motivated individual with significant experience in clinical trials of investigational medicinal products to provide efficient regulatory / administrative support, providing expert advice and procedural guidance. The main duties will include managing and scheduling clinical trials and research studies, oversight of regulatory compliance, and training.

WHAT YOU WOULD BE DOING

• Oversee each clinical project setup to completion, ensuring the smooth running of the trial and compliance with regulatory and contractual requirements
• Ensure that trials, once funded, are scheduled optimally to enable the study to proceed according to the timelines
• Assist with the development of protocols and trial related documents for studies
• Activities encompass all aspects of the conduct of clinical trials from initial design through to successful delivery and dissemination of CHART provides expertise in trial methodology and management across several key disease areas including cancer & haematological diseases to ensure that the regulatory, legal and quality control aspects of trials are met.