Support the education initiatives of the Centre to achieve quality and consistency in regulatory training for Asia Pacific
Contribute to sourcing for relevant content in accordance to the objectives and learning outcomes of the regulatory training programmes, and ensure the materials for the programme are of the required professional standard and pedagogy
Contribute to the development of the content materials and alignment to current competency expectations and skills development framework
Assist in maintaining a network of relevant regulatory experts as resources in sustaining quality in delivery of training programmes
Degree in life sciences and biomedical sciences
Active participation and contribution to preparation of education materials in a relevant setting
Recent experience involving the regulation and/or evaluation of health products (pharmaceuticals, biologics and/or medical devices) will be a major advantage
Ability to source and critique materials, assess relevance to objectives and accurately identify key learning points
Adept at constructing materials to effectively communicate key learning points, targeted at the defined audience for the training programmes
Exhibit flexibility to manage different formats of delivery methods to optimise the learning experience of the programmes
Accreditation from relevant external organisations eg. Regulatory Affairs Professionals Society (RAPS) will be an advantage.
We regret that only shortlisted candidates will be notified.