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Noncoding RNAs in Alzheimers Disease and Related Dementias (R01 Clinical Trial Not Allowed)

Funding Opportunity RFA-AG-23-010 from the NIH Guide for Grants and Contracts. The goal of this Funding Opportunity Announcement (FOA) is to stimulate research in noncoding ribonucleic acids (ncRNAs) to investigate the causality, directionality, mechanisms, and therapeutic potential of ncRNAs in Alzheimer's disease and Alzheimer's disease related dementias (AD/ADRD). This FOA will support applications seeking to discover novel mechanisms mediated by ncRNAs, elucidate molecular, and cellular functions involved in the pathogenesis and progression of AD/ADRD.

RESEARCH SPECIALIST - University of Wisconsin–Madison - Madison, WI

Indeed.com - Bioinformatics - Fri, 2022-02-25 19:57
UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department. Collects data and monitors test results.
From University of Wisconsin–Madison - Sat, 26 Feb 2022 00:57:26 GMT - View all Madison, WI jobs
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Implementing Comprehensive HIV services in Syringe Service Program (SSP) Settings (R01 - Clinical Trial Required)

Funding Opportunity RFA-DA-23-006 from the NIH Guide for Grants and Contracts. There has been a substantial increase in the number of syringe service programs (SSPs) in the US and the range of these settings has become broader, with many now located in health department or FQHCs, in addition to the more traditional CBO and AIDS Service Organization settings. There is a need to provide models for bringing sustainable integrated HIV prevention and care into SSP settings. Newer SSPs often are in settings that have limited expertise for other substance use services and may be limited in terms of HIV care. More established SSPs may provide HIV testing, but often do not directly provide other HIV prevention and care services and rely on referrals with limited follow-up. SSPs provide opportunities for regular contact with PWID and their network members (including non-injectors) which may enable greater engagement and re-engagement across the HIV continua of prevention and treatment. Newer SSPs often are in rural areas with limited capacity to provide a range of HIV services and the COVID pandemic has required restructuring of services and has led to some closures. CDC is developing infrastructure to better monitor SSP programs, survey clients, and develop technical assistance models for SSPs. A program of implementation-focused research to improve HIV prevention and care would complement this effort, as well as SAMHSAs support of these settings.

Implementing Comprehensive HIV services in Syringe Service Program (SSP) Settings (R34 - Clinical Trial Required)

Funding Opportunity RFA-DA-23-007 from the NIH Guide for Grants and Contracts. There has been a substantial increase in the number of syringe service programs (SSPs) in the US and the range of these settings has become broader, with many now located in health department or FQHCs, in addition to the more traditional CBO and AIDS Service Organization settings. There is a need to provide models for bringing sustainable integrated HIV prevention and care into SSP settings. Newer SSPs often are in settings that have limited expertise for other substance use services and may be limited in terms of HIV care. More established SSPs may provide HIV testing, but often do not directly provide other HIV prevention and care services and rely on referrals with limited follow-up. SSPs provide opportunities for regular contact with PWID and their network members (including non-injectors) which may enable greater engagement and re-engagement across the HIV continua of prevention and treatment. Newer SSPs often are in rural areas with limited capacity to provide a range of HIV services and the COVID pandemic has required restructuring of services and has led to some closures. CDC is developing infrastructure to better monitor SSP programs, survey clients, and develop technical assistance models for SSPs. A program of implementation-focused research to improve HIV prevention and care would complement this effort, as well as SAMHSAs support of these settings.

Studies of Cytosolic DNAs in the Interactions of Aging Hallmarks (R01 Clinical Trial Not Allowed)

Funding Opportunity RFA-AG-23-015 from the NIH Guide for Grants and Contracts. This Funding Opportunity Announcement (FOA) invites applications on novel studies of the cytosolic DNA sensing mechanisms in the interactions of the aging hallmarks. The goal of this FOA is to support applications that will lead to an in-depth understanding of the molecular mechanisms that determine the effects of cytosolic DNAs on aging hallmarks in the context of aging and longevity. Research supported by this FOA should lead to new insights to address some critical mechanistic questions relevant to the role of aging hallmarks in aging and aging-related diseases. This FOA encourages innovative, mechanistic approaches to identify and characterize interactions of aging hallmarks mediated by cytosolic DNAs that ultimately modulate the regulation of healthspan and/or longevity.

Mapping Interconnectivity Among Hallmarks of Aging under Lifespan Modifications (R01 Clinical Trial Not Allowed)

Funding Opportunity RFA-AG-23-013 from the NIH Guide for Grants and Contracts. This Funding Opportunity Announcement (FOA) solicits research projects with the goal of increasing our understanding of the interactions among hallmarks of aging and their regulation. Research supported by this FOA should explore the timing and possible priorities (hierarchy) among the hallmarks in various cells/tissues across the normal lifespan, and whether the interactions between the hallmarks are an adaptive response to maintain health at different stages of life. This is one of three inter-connected FOAs with an overarching focus on the interactions of aging hallmarks as a framework for innovative research in aging biology.

Inter-Organelle Communication as a Platform to Interrogate the Interactions of Hallmarks of Aging (R01 Clinical Trial Not Allowed)

Funding Opportunity RFA-AG-23-012 from the NIH Guide for Grants and Contracts. This Funding Opportunity Announcement (FOA) encourages innovative, mechanistic approaches to identify and characterize interactions of aging hallmarks shaped by inter-organelle communication.

EMBL: Senior Digital Product Designer

New Scientist - Bioinformatics - Fri, 2022-02-25 09:07
Competitive Salary: EMBL: We are looking for an experienced and energetic Senior Digital Product Designer to join EMBL’s European Bioinformatics Institute (EMBL-EBI) in our mis Hinxton, Cambridgeshire, England
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EMBL: Administrative Assistant (Full or Part Time)

New Scientist - Bioinformatics - Fri, 2022-02-25 09:03
Competitive Salary: EMBL: ELIXIR is seeking an experienced Administrative Assistant to join the international team at the ELIXIR Hub in Hinxton, UK on either a full time or par Hinxton, Cambridgeshire, England
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EMBL: Research Support Officer

New Scientist - Bioinformatics - Fri, 2022-02-25 09:03
Competitive Salary: EMBL: EMBL's European Bioinformatics Institute (EMBL-EBI) is seeking a Research Support Officer to assist the Service Team Leaders leading EMBL-EBI’s resour Hinxton, Cambridgeshire, England
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EMBL: Postdoctoral Fellow - Bioinformatics

New Scientist - Bioinformatics - Fri, 2022-02-25 09:02
Competitive Salary: EMBL: The Steinmetz group at EMBL Heidelberg is looking for an ambitious computational fellow (postdoc or research scientist, depending on the level of expe Germany (DE)
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Administrative Supplements to Support Cancer Disparity Collaborative Research (Clinical Trial Optional)

Funding Opportunity PAR-22-114 from the NIH Guide for Grants and Contracts. The purpose of this trans-NCI Funding Opportunity Announcement (FOA) is to promote new cancer disparities research among investigators who do not normally conduct it and to encourage the partnership of experienced cancer research investigators with cancer disparities-focused researchers. This FOA is intended to accelerate and strengthen multi-disciplinary cancer disparities research in wide ranging areas. Cancer disparities research includes, but is not limited to basic, translational, behavioral, observational, interventional, environmental and population research studies that address the adverse differences in cancer incidence, prevalence, mortality, survivorship, burden and/or response to treatment in racial/ethnic minorities and/or underserved population groups. Proposed collaborations should focus on achieving research objectives that by necessity rely on diverse and complementary expertise, technical capabilities, and resource sets. Importantly, the supplemental request is required to be within the scope of the parent award and should expand the original aims to include a cancer disparity component and possible inclusion of international comparator cohorts. A trans NCI effort, the concept reissuance of the Collaborative Program is supported by NCIs Division of Cancer Biology (DCB), Division of Cancer Treatment and Diagnosis (DCTD), Division of Cancer Prevention (DCP), Division of Cancer Control and Population Sciences (DCCPS), Center to Reduce Cancer Health Disparities (CRCHD) and now, also included Center for Global Health.

Research Technologist II - Medical College of Wisconsin - Milwaukee, WI

Indeed.com - Bioinformatics - Thu, 2022-02-24 16:14
Carry out routine and complex experiments and data analysis. Participate in the analysis of omics data. Participate in cell and molecular research as directed…
From Medical College of Wisconsin - Thu, 24 Feb 2022 21:14:04 GMT - View all Milwaukee, WI jobs
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SRG: Senior Scientist - R&D - NGS

New Scientist - Bioinformatics - Thu, 2022-02-24 12:18
GBP42000.00 - GBP55000.00 per annum: SRG: R&D opportunity! London, England
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Immune Drivers of Autoimmune Disease (IDAD) (U01 Clinical Trial Not Allowed)

Funding Opportunity RFA-AI-22-012 from the NIH Guide for Grants and Contracts. This Funding Opportunity Announcement (FOA) invites applications to participate in the Immune Drivers of Autoimmune Disease (IDAD) cooperative research program, which will focus on defining the immunologic states and dynamics that drive autoimmune disease. The main objective of this program is to enhance our understanding of the immunologic processes, events, and changes that underlie the clinical manifestations of autoimmune diseases, including disease flare, remission, and progression of established disease, as well as the progression from a state of elevated risk to clinical diagnosis of autoimmune disease.

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