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Offer Description
Key Responsibilities
The research group of Prof. Bob van de Water aims to unravel cell signaling programs that underlie adverse xenobiotic-induced adverse responses as well as anticancer drug resistance. In particular, high throughput transcriptomics analysis is applied with innovative co-regulated gene network analysis thus contributing to a system toxicology approach in qualifying and quantifying adverse responses.
We are seeking a candidate with a strong interest in bringing toxicogenomics to the next level by improving its interpretation and dose-response analysis and FAIRification.
In this project the candidate will work on innovative (data) approaches within PARC (Partnership for the Assessment of Risks from Chemicals), actively participating in further implementation of the co-regulated gene networks framework for chemical hazard assessment. In particular, the candidate will design approaches to improve interpretation of gene co-expression modules, including defining ontologies (connecting to the AOP framework) and implementing benchmark dose analysis for gene network analysis.
In addition, the candidate will be (jointly) responsible for the implementation of PARC FAIR Research Data Management (RDM) policies developed through the PARC project. This includes alignment of the above-described research with FAIR principles, and FAIRification of the OMICS workflow. You will also advise researchers involved in the PARC project on compliance with the FAIR data and Open Science principles in all stages of the research cycle: collection, storage, archiving, and reuse of data. You will provide support in the writing of Research Data Management Plans for the PARC researchers, as well as training, workshops, communication, guidelines, and checklists. You will also contribute to developing an excellent data infrastructure (local, national and international).
The prospective candidate will join an enthusiastic research team of >25 researchers that conduct their work in the context of multiple past and current European-funded projects (EU-ToxRisk, RISK-HUNT3R, eTRANSAFE, TransQST, VHP4Safety, PARC, DISCERN) and grants funded by the EFSA (TD-TRAQ, TXG-MAP), where successful interactions between academia, industry, and regulatory agencies assure excellent scientific and societal impact, as well as a strong support network.
The successful applicant will:
Requirements
Specific Requirements
Selection criteria
Additional Information
Benefits
Terms and conditions
We offer a full-time, one year term position, with the possibility of renewal for an additional maximum of three years based on performance. Salary range from € 3.226,- to € 5.090,- gross per month, depending on experience (pay scale 10 in accordance with the Collective Labour Agreement for Dutch Universities).
Leiden University offers an attractive benefits package with additional holiday (8%) and end-of-year bonuses (8.3 %), training and career development and sabbatical leave. Our individual choices model gives you some freedom to assemble your own set of terms and conditions. Candidates from outside the Netherlands may be eligible for a substantial tax break. For more information ( https://www.universiteitleiden.nl/en/working-at/job-application-procedure-and-employment-conditions ), see the website.
Selection process
Applications
To apply for this vacancy, please submit your application online via the blue button in our application system.
Please ensure that you upload the following additional document quoting the vacancy number:
Only applications received before 15 February 2024 can be considered.
Additional comments
Information
Inquiries can be made to Bob van de Water (b.water@lacdr.leidenuniv.nl ), Giulia Callegaro (g.callegaro@lacdr.leidenuniv.nl ) and/or Sylvia Le Dévédec (s.e.ledevedec@lacdr.leidenuniv.nl ). If you have any questions about the procedure, please contact the secretariat of the Division of Drug Discovery & Safety, Marjolijn Lugthart (m.j.l.lugthart@lacdr.leidenuniv.nl ).
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STATUS: EXPIRED
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