Job Watch
Innovation Corps (I-Corps) at NIH Program for NIH and CDC Translational Research (Admin Supp - Clinical Trial Not Allowed)
Funding Opportunity PA-18-517 from the NIH Guide for Grants and Contracts. This funding opportunity announcement (FOA) seeks to develop and nurture a national innovation ecosystem that builds upon biomedical research to develop technologies, products and services that benefit society. Toward meeting this objective, the I-Corps program is being offered. The I-Corps at NIH program is focused on educating researchers and technologists on how to translate technologies from the lab into the marketplace. Under this FOA, participating NIH and CDC Institutes and Centers will continue providing administrative supplement awards to currently-funded SBIR and STTR Phase I grantees. The program is designed to provide three-member project teams with access to instruction and mentoring in order to accelerate the translation of technologies currently being developed with NIH and CDC SBIR and STTR funding. It is anticipated that outcomes for the I-Corps teams participating in this program will include significantly refined commercialization plans and well-informed pivots in their overall commercialization strategies. Prospective applicants are strongly encouraged to contact NIH or CDC Scientific/Research staff for more information about the program before applying.
Categories: Job Watch, Literature Watch
Revision: NIH Policy and Guidelines on the Inclusion of Individuals Across the Lifespan as Participants in Research Involving Human Subjects
Notice NOT-OD-18-116 from the NIH Guide for Grants and Contracts
Categories: Job Watch, Literature Watch
NIH Operates Under a Continuing Resolution Through December 22, 2017
Notice NOT-OD-18-120 from the NIH Guide for Grants and Contracts
Categories: Job Watch, Literature Watch
Ancillary Studies to the NIDDK Inflammatory Bowel Disease Genetics Consortium (R01- Clinical Trial Optional)
Funding Opportunity RFA-DK-17-017 from the NIH Guide for Grants and Contracts. The NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC), in collaboration with the International IBD Genetics Consortium, has identified about 200 susceptibility loci for IBD. The IBDGC has recently been awarded renewed funding to identify causal genes and genetic variants within these loci, and to elucidate the mechanisms through which they contribute to the pathophysiology of IBD. However, the IBDGC's current resources permit them to explore the functions of only a limited set of genes within a limited set of physiological domains. The purpose of this FOA is to expand the number of genes and range of IBD-related phenotypes and physiological domains under study by means of collaborations of the IBDGC with investigators with expertise complementary to that of their own members. Proposed studies must not duplicate studies either ongoing or already completed by the IBDGC. Multi-site clinical trials will not be considered responsive to this FOA.
Categories: Job Watch, Literature Watch
Ancillary Studies to the NIDDK Inflammatory Bowel Disease Genetics Consortium (R21 - Clinical Trial Optional)
Funding Opportunity RFA-DK-17-018 from the NIH Guide for Grants and Contracts. The NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC), in collaboration with the International IBD Genetics Consortium, has identified about 200 susceptibility loci for IBD. The IBDGC has recently been awarded renewed funding to identify causal genes and genetic variants within these loci, and to elucidate the mechanisms through which they contribute to the pathophysiology of IBD. However, the IBDGC's current resources permit them to explore the functions of only a limited set of genes within a limited set of physiological domains. The purpose of this FOA is to expand the number of genes and range of IBD-related phenotypes and physiological domains under study by means of collaborations of the IBDGC with investigators with expertise complementary to that of their own members. This FOA is intended to support highly exploratory studies which may require development and testing of novel experimental platforms or analytic methods. Proposed studies must not duplicate studies either ongoing or already completed by the IBDGC. Multi-site clinical trials will not be considered responsive to this FOA.
Categories: Job Watch, Literature Watch
Notice Announcing the Removal of the Funding Pause for Gain-of-Function Research Projects
Notice NOT-OD-17-071 from the NIH Guide for Grants and Contracts
Categories: Job Watch, Literature Watch
Sr Product Development Scientist - BloodCenter of Wisconsin - Milwaukee, WI
DNA and RNA isolation, conventional and real-time PCR, quantitative and qualitative reverse transcriptase PCR (RT-PCR), automated DNA sequencing and fragment...
From BloodCenter of Wisconsin - Tue, 19 Dec 2017 09:54:50 GMT - View all Milwaukee, WI jobs
From BloodCenter of Wisconsin - Tue, 19 Dec 2017 09:54:50 GMT - View all Milwaukee, WI jobs
Categories: Job Watch
Bioinformatics Student Worker - BloodCenter of Wisconsin - Milwaukee, WI
Experience working with open-source and or vendor-supplied software programs for bioinformatics data analysis is desirable....
From BloodCenter of Wisconsin - Tue, 19 Dec 2017 09:52:51 GMT - View all Milwaukee, WI jobs
From BloodCenter of Wisconsin - Tue, 19 Dec 2017 09:52:51 GMT - View all Milwaukee, WI jobs
Categories: Job Watch
EMBL: Project Manager - Heidelberg Center for Human Bioinformatics (HD-HuB)
Competitive Salary:
EMBL:
Project Manager - Heidelberg Center for Human Bioinformatics (HD-HuB)Location:Heidelberg, GermanyStaff Category:Staff MemberContract Duration:2 years (part-time)Grading:5Closing Date:31 January 2018Reference Number:HD_01222Job Description
The European Mo
Germany (DE)
Categories: Job Watch
Human Cell Biology of Alzheimer's Disease Genetic Variants (R01 - Clinical Trial Not Allowed)
Funding Opportunity PAR-18-516 from the NIH Guide for Grants and Contracts. The goal of this FOA is to establish functional genotype-phenotype relationships of genetic variants, suspected of altering the risk of Alzheimers disease (AD), in neural cells using human induced pluripotent stem cells or other human cell reprogramming approaches. The causal linkage of AD-associated genetic variants identified in genome-wide association studies and genome sequencing studies to molecular and biological cell phenotypes in human neural cells is expected to give greater insight into molecular targets contributing to the etiology of AD. Studies of human genetics in human cells is essential to understanding the etiology of AD.
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Notice of Change to Receipt Date on NIH-CASIS Coordinated Microphysiological Systems Program for Translational Research in Space (UG3/UH3 Clinical Trials Not Allowed) (RFA-TR-18-001)
Notice NOT-TR-18-014 from the NIH Guide for Grants and Contracts
Categories: Job Watch, Literature Watch
Discovery of Molecular Targets for Pregnancy-Related/Induced Diseases and Development of Therapeutics to Prevent/Treat These Diseases (R01 - Clinical Trial Optional)
Funding Opportunity PAR-18-511 from the NIH Guide for Grants and Contracts. The purpose of this funding opportunity announcement (FOA) is to encourage grant applications that will identify molecular targets for pregnancy associated/induced disorders and will lead to the development of new safer and more effective medications for use in pregnancy.
Categories: Job Watch, Literature Watch
Henry M Jackson Foundation: Postdoctoral Fellow (Cancer Therapy)
Competitve Salary:
Henry M Jackson Foundation:
Henry M Jackson, Rockville, MD seeks a Post-doctoral Fellow for the Uniformed Services University (USU) Center for Prostate Disease Research (CPDR)
Rockville, Maryland
Categories: Job Watch
Drug Repurposing for Conditions Affecting Neonates and Pregnant Women (R01 - Clinical Trial Optional)
Funding Opportunity PAR-18-506 from the NIH Guide for Grants and Contracts. The purpose of this funding opportunity announcement (FOA) is to repurpose already FDA approved drugs for new neonatal and obstetric indications, in order to overcome the difficulties associated with the traditional development of drugs appropriate for use in neonates and pregnant women and facilitate treatment of these vulnerable populations.
Categories: Job Watch, Literature Watch
Community Partnerships to Advance Research (CPAR) (R21 Clinical Trial Optional)
Funding Opportunity PA-18-381 from the NIH Guide for Grants and Contracts. This funding opportunity announcement (FOA) encourages researchers to partner with community groups, using Community Engaged Research (CEnR) methodologies that will enhance relationships and lead to better intervention development and positive health outcomes.
Categories: Job Watch, Literature Watch
Community Partnerships to Advance Research (CPAR) (R01 Clinical Trial Optional)
Funding Opportunity PA-18-377 from the NIH Guide for Grants and Contracts. This funding opportunity announcement (FOA) encourages researchers to partner with community groups, using Community Engaged Research (CEnR) methodologies that will enhance relationships and lead to better intervention development and positive health outcomes.
Categories: Job Watch, Literature Watch
Community Partnerships to Advance Research (CPAR) (R15 Clinical Trial Not Allowed)
Funding Opportunity PA-18-475 from the NIH Guide for Grants and Contracts. This funding opportunity announcement (FOA) encourages researchers to partner with community groups, using Community Engaged Research (CEnR) methodologies that will enhance relationships and lead to better intervention development and positive health outcomes.
Categories: Job Watch, Literature Watch
Advancing Basic Neurobiology Toward Translation Through Assay Development (R01 Clinical Trials Not Allowed)
Funding Opportunity PAR-18-505 from the NIH Guide for Grants and Contracts. This funding opportunity announcement (FOA) encourages research grant applications to develop novel, robust assays to reveal changes in neuronal and/or glial function. The goal is to adapt state-of-the-art measures of basic cellular processes or molecular events that are key mediators of nervous system function into phenotypic assays, with the intent to probe mechanisms or perturbations in an unbiased and efficient manner. These novel assays would provide opportunities to measure neurobiological endpoints to accelerate basic discovery and support target identification and therapeutic development efforts.
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Notice of Participation of the National Institute of Environmental Health Sciences in PA-18-397 "NIH Pathway to Independence Award (Parent K99/R00 - Independent Clinical Trial Required"
Notice NOT-ES-18-006 from the NIH Guide for Grants and Contracts
Categories: Job Watch, Literature Watch
Notice of Clarification of NINDS Statement of interest for "Bioengineering Research Partnerships (BRP) (U01 Clinical Trial Optional)"
Notice NOT-NS-18-029 from the NIH Guide for Grants and Contracts
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