Postdoc in Regulatory Science Focusing on The Development of An Infrastructure for Real-Time Analytics of Regulatory Documents [closing 01May2021]

Страна: Дания;

Город: Copenhagen

Добавлена: 10.04.2021

Работодатель: The Copenhagen Centre for Regulatory Sciences (CORS), Department of Pharmacy

Тип: PostDoc vacancy;

Для кого: For researchers;

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Дедлайн подачи: 01.05.2021

 

The Copenhagen Centre for Regulatory Sciences (CORS), Department of Pharmacy is offering a 1½ year fulltime Postdoc fellowship in Regulatory Science on a project aiming at developing an infrastructure for real-time analytics of medicine regulatory processes.

The fellowship is available from May 1, 2021 or the soonest possible thereafter.

CORS

We offer an interesting and challenging job in at CORS, an international cross-disciplinary research environment spanning pharmacy, humanities, law, and social science. At CORS, we strive for academic excellence, collegial respect, and freedom tempered by responsibility. With its research, CORS seeks to improve the drug regulatory system, by systematically studying its structure and behaviour as well as designing new tools to facilitate regulatory decision-making. Through improvement of the drug regulatory system, we aim to contribute to an improvement of the health of the society.

You can read more about CORS here: https://cors.ku.dk/ 

Project description

Regulatory science often use data captured in existing, publicly accessible government sites. These data capture many attributes of a medicine regulatory processes and drug development, ranging from clinical trial information to post-marketing assessments of safety and effectiveness, risk management plans, regulatory review, and agency interactions.

However, this information is typically spread across multiple documents, much still in unstructured formats, making data collection cumbersome and time-consuming and making it challenging to link information, and sometimes also to validate the accuracy of the data.

This project aims at exploring the feasibility, sustainability and usability of creating and maintaining a regulatory science database that in a (semi-) automated manner by collecting unstructured data from public available regulatory resources and transform them in structured data ready to be sequentially analysed.

The database should support the development of a publicly available user interface (e.g., dashboard) to conduct (near) real-time descriptive analytics of regulatory documents.

Novo Nordisk A/S finances the fellowship.

Your job

Your key tasks as a postdoc at the Faculty are to:

  • Develop a publicly available user interface (e.g., dashboard) to conduct (near) real-time descriptive analytics of regulatory documents
  • Write scientific manuscripts on the grounds of your research results
  • Participate in Center activities
  • Participate in national and international conferences and scientific meetings
  • Participate in teaching activities at the department
  • Co-supervise PhD and MSc students 
 
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