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Project sheet

Name

Assistant Researcher in medicinal and biological chemistry and computational biochemistry.

Total project amount

82,25 thousand €

Amount paid

82,25 thousand €

Non-refundable funding

82,25 thousand €

Loan funding

0 €

Start date

01.04.2025

Expected end date

31.03.2026

Dimension

Resilience

Component

Qualifications and Skills

Investment

Science Plus Training

Operation code

02/C06-i06/2024.P2023.15700.TENURE.030

Summary

Auxiliary Researcher position aligned with the thematic lines MedLife and MolCat and, in particular omics-supported medicinal and biological chemistry and computational biochemistry.??????? Rationale for the position:The rationale for this profile roots in specific expertise and skills required to advance the scientific strategy of CQE. The candidate is expected to play a crucial role in the integration of two thematic lines, MEDLife – Medicinal and Biological Chemistry for Health, and MolCat – Molecular and Catalyst Design. By focusing on health-promoting strategies through advanced mass spectrometry and computational biochemistry, and by exploring mechanisms of drug resistance and of microbial resistance, and by elucidating links between infections and non-communicable diseases (NCDs), the researcher will directly support CQE’s commitment to addressing health challenges. The involvement in medicinal chemistry, molecular design, and the development of health-focused drugs aligns with MolCat´s focus on precision molecular design and the creation of active molecules.This research area is embedded in SDG 3, ´Good Health and Well-being,´ focusing on health-promoting strategies. It significantly contributes to SDG9, ´Industry, Innovation, and Infrastructure,´ through novel drug development, advanced biological chemistry, and multi-omics capabilities. The emphasis on personalized medical approaches also addresses health inequalities, contributing to SDG10 ´Reduced Inequalities´ and SDG16 ´Peace, Justice, and Strong Institutions.CQE´s strategy relies strongly in studying drug resistance mechanisms using advanced biochemical and multi-omics tools, addressing microbial resistance, cancer mechanisms, and contributing to the development of novel drug scaffolds. This aims to understand links between infection and NCDs, employing systems biology for personalized medical approaches. This strategy stems from the ESFRI Roadmap and is primarily aligned with the EU Roadmap on Non-Communicable Diseases, with translation into the Health First Europe and the Small Countries Initiative Roadmaps, significantly contributing to the One Health approach. Incorporated in the ISIDORe network, and within the scope of ERINHA, EATRIS and MIRRI research infrastructures, this research area also advances research on epidemic-prone diseases. Tasks to be performed:This position is geared towards the advancement of health-promoting strategies through an integrative medicinal and biological chemistry, focused on biological mass spectrometry, and molecular design, towards the discovery of novel drug candidates, bringing together the MedLife and MolCat thematic line.Tasks:Plan, coordinate, develop, and publish research work, in the research areas defined above, centered on biological mass spectrometry, computational biochemistry (such as molecular dynamics), medicinal chemistry (particularly drug design), and multi-omics approaches within a systems biology paradigm, integrating mass-spectrometry derived proteomics and metabolomics with inferred links to the genome and transcriptome, to gain a comprehensive understanding of biological systems.Design and submit project proposals for funding at national/international levels.Involve students in research and supervise master’s dissertations and doctoral thesis.Establish contacts with industry and healthcare stakeholders, for joint projects and knowledge transfer.Engage in scientific dissemination activities for peers, students, and general public.Create, expand and maintain mass spectrometry laboratory infrastructures for research. Scientific profile required:The hired researcher should have experience in:mass spectrometry, both at the structural analysis level, particularly at drug and drug metabolite analysis, and at the omics level, centered on both proteomics and metabolomics data acquisition and bioinformatics-supported data analysis and integration.computational biochemistry, geared towards protein-drug interactions.Candidates must demonstrate their ability for hands-on use of the installed capacities at CQE, bringing together all valences to contribute to the research goals. In parallel, candidates must demonstrate their collaboration track and interdisciplinary skills, bridging the gap between medicinal chemistry, biological mass spectrometry, and computational approaches, and establishing bridges with chemistry-oriented researchers at CQE, partner institutions, and with the clinical community. The researcher is also expected to identify and apply to infrastructure funding calls to leverage and expand CQE’s installed capacity.

Beneficiaries

Within the scope of the Recovery and Resilience Plan, two types of beneficiaries are responsible for carrying out the projects and using the funding provided. Due to their similar role, the reference to these two types of beneficiaries has been simplified and unified under the term "Beneficiary".
The two types are::
  • Direct Beneficiaries are those whose funding and projects to implement are part of the Recovery and Resilience Plan that has been negotiated and approved by the European Union;
  • Final Beneficiaries are those whose funding and projects to implement are approved following a selection process through Calls for Applications.

Call for applications

As part of the Call for Applications, submissions are requested to select the projects and final beneficiaries to whom funding will be awarded. Specific selection criteria are defined for each call, which must be reflected in the applications submitted and assessed.

The project is appraised on the basis of its compliance with the selection criteria laid down in the calls for applications, and a final score may be awarded, where applicable.

Final evaluation score

9,1
Important note

The components for calculating the assessment score can be found in the selection criteria document mentioned below.

Selection criteria

The funding selection criteria to which this project and its final beneficiary were subject and its score can be found in detail on the Recuperar Portugal platform.

Beneficiaries

Intermediate beneficiaries

Beneficiaries

Procurement

Beneficiaries representing public entities implement their project by signing one or more contracts with suppliers for goods or services through public procurement procedures.

To ensure and provide the utmost transparency in all these contracts, a list of the contracts that were signed under this project is available here, along with the information available on the Base.Gov platform. Please note that, according to the legislation in force at the time the contract was signed, some exceptions do not require the publication of the contracts signed on this platform, and, therefore, no information is available in such cases.

Geographic distribution

82,25 thousand €

Total amount of the project

Percentage of the amount already paid for implementing projects

, 100 %,

Where was the money spent

By county

1 county financed .

  • Lisboa 82,25 thousand € ,
Source EMRP
10.02.2026
All themes
Transparency without leading