Chairman, Cyclotron & Radiopharmaceuticals

• Extensive knowledge and experience of the production of cyclotron and reactor radiopharmaceuticals according to the international guidelines of Good Manufacturing Practice (GMP).
• Extensive knowledge and experience of the Quality Control (QC) and Quality Assurance (QA) of radiopharmaceuticals according to international regulatory requirements.
• A good track record of writing and reviewing suitable scientific reports & documentation to fulfill radiopharmaceuticals and radiation protection regulatory requirements.
• Extensive experience in the development and validation of novel radio labeled theranostic agents through pre-clinical studies, and in cyclotron technology.
• Ability of providing knowledge and guidance in the safety and efficacy of the new radiopharmaceuticals to be used clinically.
• Ability to play a key role in research projects with clinician, academic partners and external contract research and development organizations.

Doctor of Philosophy (PhD) or equivalent in scientific discipline with a strong background in cyclotron and radiopharmaceuticals from an accredited university/institution is required.

Twelve (12) years post doctorate research experience as an independent professional with at least five (5) years extensive administrative/supervisory experience is required.

Research productivity must be demonstrated in a form of publications in reputable relevant peer reviewed journals.