Employment Opportunities

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Post-doctoral position in RNA Biology/Alternative Splicing

A post-doctoral position is available for a qualified individual to carry out studies in the field of alternative splicing. A focus of the research will be on novel epithelial cell-type-specific splicing proteins (Esrp1 and Esrp2) that were identified in our lab in a cell-based genetic screen (Molecular Cell 33(5):591-601 (2009). We have use high throughput sequencing and other genome-wide technologies to identify global programs of alternative splicing in epithelial cells that are abolished upon Esrp depletion (Embo J. 29(19): 3286-3300; Mol. Cell. Biol. 32(8): 1468-1482). The research project will extend the use of genome-wide sequencing technologies to study programs of alternative splicing that are altered in newly developed Esrp1/Esrp2 KO mice, which display disease related phenotypes. Further details about the lab can be accessed at: http://www.med.upenn.edu/camb/faculty/ggr/carstens.html. The position requires an M.D. or Ph.D. degree. Previous experience in mouse genetics, RNA biology, and molecular or cell biology is preferred. Please send a CV including at least two references to: Dr. Russ P. Carstens, University of Pennsylvania School of Medicine, 575 Clinical Research Building, 415 Curie Blvd. Philadelphia, PA 19104, [email protected].

Position Available in the Lab of Dr. Jacob Schwartz at the University of Arizona in Tucson, AZ

An exciting postdoctoral fellow position is available in the lab of Dr. Jacob Schwartz at the University of Arizona in Tucson, AZ, to study the role of RNA binding proteins in regulating transcription and DNA damage response. Specific projects include the role of RNA binding proteins in Lou Gehrig’s disease, Ewing sarcoma, and the role of noncoding RNAs in regulating transcription. Candidates with a strong background in molecular biology, biochemistry, or computational biology are encouraged to apply. The lab’s research focus ranges from protein purification, cell culture, primary neuronal cell culture, and whole mouse studies. Techniques include mass spectrometry, protein/RNA structure functional studies, immunofluorescence and microscopy, and next-generation sequencing. To apply please send a CV and letter of interest with the contact information for your references to [email protected].


Relevant Publications:
1. Schwartz JC, Cech TR, Parker RR, “Biochemical properties and biological functions of FET proteins”, Annu. Rev. Biochem. 2015; 84 (Epub ahead of print)
2. Schwartz JC, Podell ER, Han SSW, Berry JD, Eggan KC, Cech TR, “FUS is sequestered in nuclear aggregates in ALS patient fibroblasts” Mol Biol Cell, 2014; 25(17):2571-8. (PMID: 25009283)
3. Schwartz JC, Wang X, Podell ER, Cech TR, “RNA seeds higher order assembly of FUS protein” Cell Reports, 2013; 5(4):918-25.
4. Schwartz JC, Ebmeier CC, Podell ER, Heimiller J, Taatjes DJ, Cech TR, “FUS binds the CTD of RNA polymerase II and regulates its phosphorylation at Ser2” Genes Dev, 2012; 26:2690-95.
5. Schwartz, JC, Younger, S, Nguyen,N, Hardy, D, Monia, BP, Corey, DR, Janowski, BA, “Antisense Transcripts are Targets for Small Activating RNAs”, Nat Struct Mol Biol. 2008 Aug;15(8):842-8.

Postdoctoral position to study the functions and regulation of localized RNAs

A postdoctoral position to study the functional roles and regulation of localized RNAs is available immediately in Dr. Stavroula Mili’s lab at the National Cancer Institute, National Institutes of Health, Bethesda, MD. The lab is interested in understanding the regulation of RNA localization by cancer-associated proteins and the contribution of localized RNAs to tumor progression. The work relies on a variety of cell biological, microscopical and biochemical approaches in 2D and 3D cell culture systems. The research program is funded by the NIH Intramural program and is supported by state-of-the-art facilities on the NIH campus.

Interested candidates must have received a Ph.D. degree in cell biology, biochemistry or related discipline, and be highly motivated to design and pursue innovative research directions.

Applications should include a CV, description of research interests and prior accomplishments, contact information of at least 3 references and preferred start date. Please e-mail application materials to [email protected]

The NIH is dedicated to building a diverse community in its training and employment programs.

DHHS/NIH is an Equal Opportunity Employer.

Contribute to NIH-R01 Funded Projects Focused on mRNA Decay in Myotonic Dystrophy and Pluripotent Stem Cells

We are looking for an enthusiastic and hard-working post-doctoral fellow to contribute to NIH-R01 funded projects focused on mRNA decay in myotonic dystrophy and pluripotent stem cells. The projects aim to identify novel changes in mRNA metabolism that contribute to pathogenesis and pluripotency. State-of-the-art genome-wide approaches and other molecular techniques will be employed using primary and stem cells.

The successful candidate should hold a PhD and/or MD and have less than 5 years post-doctoral experience in the general area of cell and molecular biology. Preference will be given to those with experience in RNA biology, genome-wide approaches and/or stem cell biology. Bioinformatics expertise is highly desirable. The fellow will report to Jeff and Carol Wilusz, but will be expected to work somewhat independently. S/he will be encouraged to apply for fellowship funding and given the opportunity to train junior researchers. Excellent technical, oral and written communication skills are essential.

The Wilusz lab has extensive expertise in all aspects of RNA biology linked with disease and development.

We are located at Colorado State University, in Fort Collins, Colorado – frequently voted one of the “Best Places to Live in the US”.

Apply by 3/15/2015 for full consideration, but the position will remain open until filled. The start date could be as early as 4/15/2015; funding is available through 2019.
For complete job description and to apply go to http://jobs.colostate.edu/postings/8417.

CSU is an EO/EA/AA employer and conducts background checks on all final candidates.

Faculty Position at Department of Cell and Molecular Physiology at Loyola University Chicago

The Department of Cell and Molecular Physiology at Loyola University Chicago, Health Sciences Division seeks applicants for tenure-track positions at the ASSISTANT PROFESSOR, ASSOCIATE PROFESSOR and PROFESSOR level. We seek colleagues that will contribute to existing strengths in molecular neuroscience, cardiac physiology and biophysics. Our faculty are actively engaged in research in diverse areas including membrane transport mechanisms, molecular neuroendocrinology, neuronal excitability, neurobiological effects of alcohol abuse, and RNA/epigenetic regulation in health and disease. Applicants using proteomic and genomic tools to address fundamental questions in molecular neuroscience are strongly encouraged to apply. Departmental infrastructure includes resources in mass spectrometry, fluorescence microscopy, electrophysiology, animal facilities – including a small animal VIVO 2100 ultrasound, echocardiography instruments and surgical suites, viral vector core, molecular dynamics simulation, single molecule biophysics and biophysical spectroscopy. Other instrumentation and University core facilities are described here: (http://www.stritch.luc.edu/depts/physio). Laboratory space will be located in the new Center for Translational Research and Education. The faculty applicant will be expected to sustain an independent, externally funded research program. In addition, the applicant must have evidence of teaching experience and will be expected to contribute to graduate and medical education. Candidates must have a doctoral degree and postdoctoral experience; senior applicants should have a strong record of research productivity and extramural support. Review of applications will commence immediately and applications will be accepted until the position is filled. Apply directly at http://www.careers.luc.edu/applicants/Central?quickFind=57760
Equal Opportunity Employer: Minorities/Women/Veterans/Disabled

NIH-funded Postdoctoral Fellowship Position

NIH-funded Postdoctoral Fellowship Position, to begin Oct 1, 2015 or later (duration: 2-5 yrs).
NIH-funded Postdoctoral Fellowship Position in Eukaryotic RNA Metabolism
National Institutes of Health (NIH), Bethesda, Maryland

The Fellow will investigate molecular mechanisms involved in RNA metabolism relevant to eukaryotic gene expression. Candidates must hold a Ph.D. or M.D. and have less than 5 years postdoctoral experience. Expertise in molecular biology, genetics and/or biochemistry is required, as are strong letters of recommendation. The successful candidate will confer regularly with the principal investigator but must develop self-directed research and have good technical, presentation, and communication skills as essential parts of the training experience.
Interested candidates should email a cover letter that details their specific interests in the research interests of the Maraia lab.
•Send a cover letter, C.V., and the names of three references with their email addresses and telephone numbers by Email to:
Richard J. Maraia, M.D.
Email: [email protected]

Maraia lab current interests
•mRNA biased codon use and effects of variable tRNA gene complement.
•Anticodon modification by tRNA isopentenylytransferase and its role in translation and disease.
•Molecular mechanisms of La-related protein -4 (LARP4) function in translation.
•Role of the La protein in tRNA production.
•Molecular mechanisms of transcription termination by RNA polymerase III.

Postdoctoral Research Fellow Position at the University of California, San Francisco

A postdoctoral research fellow position is available at the University of California, San Francisco at the new Helen Diller Comprehensive Cancer Center (Mission Bay Campus) (http://pub.ucsf.edu/missionbay/tour/; http://cancer.ucsf.edu/news/20031028b.php), to study the molecular mechanisms by which impairments in accurate control of mRNA translation, cell growth, and overall cellular protein synthesis rates lead to cancer. The potential candidate will utilize the first mouse models for components of the translation machinery in combination with novel proteomics and pharmacological strategies to study the dynamics of translation control in gene expression, cancer, and disease. Highly motivated individuals with a recent Ph.D., M.D. or M.D./Ph.D. and a background in mouse genetics, biochemistry, or cellular and molecular biology are encouraged to apply. Evidence of scientific accomplishment is required and bioinformatics skills are desirable. Requests should be addressed to: [email protected] and [email protected].

Please visit our webpage at ruggerolab.ucsf.edu.

Explore the Role of mRNA Expression and Distribution in Cancers Caused by Genetic Re-arrangements

One position is available immediately to explore the role of mRNA expression and distribution in cancers caused by genetic re-arrangements. This is accomplished using single molecule florescent in situ hybridization, commercially called “Stellaris probes”. Studies involve working with cancer cell lines and patient samples, in situ hybridization, fluorescence microscopy and image analysis and interpretation using MATLAB software. The project is supported by an early independence award from NIH (2012-2017)

Job requirements: Recent Ph.D. in Life science or basic science. The candidate should be self-motivated and hard working with a strong background in molecular biology. Hands on working experience in basic molecular biology techniques like cloning, culture of immortalized and primary cells, microscopy and image analysis is desired. Candidate will be responsible for designing, performing experiments, compiling and analyzing data and providing necessary help in preparation of materials for publications and grant proposals. Ability to write and submit proposals for fellowships will be a plus.
Interested candidates who are willing to join immediately, should email their CVs and contact information of three references to Mona Batish, Ph.D. Assistant Professor, Email: [email protected]

2 Postdoctoral positions available in RNA NMR at Karolinska Institute (Stockholm)

More than 50% of the human genome codes for non-coding RNA. These RNAs are ubiquitous among all life forms and the mechanisms how non-coding RNAs regulate these cellular functions are largely unknown.
Our research group is interested in understanding how RNAs change their structures in order to perform function. We employ liquid-state Nuclear Magnetic Resonance (NMR) and other biophysical and biochemical techniques, to investigate the molecular mechanism of RNA function ( Nature 2012 & 2015). When function of these molecular machines becomes apparent, it also provides a variety of unique new drug targets. The lab also develops methods in NMR and RNA biochemistry to address these questions.

Projects (each one year with possibility to extend another year):
One Postdoc will work on development of NMR experiments and/or simulations for RNA dynamics parameters. The second Postdoc will develop biochemical methods to produce larger RNAs or RNAs in environment of larger proteins (e.g. partial labeling, specific modifications). Both postdocs will work on RNAs addressing biological questions studied in the lab (microRNAs and ribosomal RNAs). You will work in a team together with other lab members and regularly present the research work in lab-meetings, seminars and at international conferences.

The projects will be supervised by Dr. Katja Petzold, deadline 31st of January 2015. Please apply directly via the netrecruiter system:
Fore more information please visit the website:

Investigate the Mechanisms and Regulation of Pre-mRNA Processing by the U12-dependent Spliceosome

The RNA splicing group at the Institute of Biotechnology, University of Helsinki, Finland is looking for a post-doctoral researcher in a project that investigates the mechanisms and regulation of pre-mRNA processing by the U12-dependent spliceosome.
A successful candidate has a PhD and strong background in molecular biology, cell biology or in a related field as shown by solid publication record in international peer-reviewed journals. Good communication skills and fluency in spoken and written English are required. An experience in RNA biology/biochemistry, bioinformatics/high throughput sequencing, and/or genome editing is an asset.
The specific projects will depend on the previous experience and the qualifications of the successful applicant but is likely include mammalian genome editing with CRISPR/CAS system combined with high-throughput sequencing to investigate the regulatory aspects of the U12-type intron splicing.
Further information of the research group and the research topic and the application form can be found from the group web site http://www.biocenter.helsinki.fi/bi/SPLICING/index.html.
In addition to the application form, the application should include a motivation letter, a CV and a list of publications (max. 1 page), all combined to a single pdf that should be attached to the application form. The deadline for applications is January 15th, 2015. The position is available immediately.
The funded position is initially for 2 to 3 years, depending on the start date.
For further information please contact Mikko.Frilander(at)Helsinki.Fi

Recent publications:
Niemelä, E.H., Oghabian, A., Staals, R.H.J., Pruijn, G.J.M., and Frilander, M.J. (2014). Global analysis of the nuclear processing of unspliced U12-type introns by the exosome. Nucleic Acids Res 42, 7358-7369.
Argente, J., Flores, R., Gutiérrez-Arumí, A., Verma, B., Martos-Moreno, G.A., Cuscó, I., Oghabian, A., Chowen, J.A., Frilander, M.J., and Pérez-Jurado, L.A. (2014). Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency. EMBO Mol Med 6, 299–306.
Turunen, J.J., Niemelä, E.H., Verma, B., and Frilander, M.J. (2013). The significant other: splicing by the minor spliceosome. Wiley Interdiscip Rev RNA 4, 61–76.
Turunen, J.J., Verma, B., Nyman, T.A., and Frilander, M.J. (2013). HnRNPH1/H2, U1 snRNP and U11 snRNP co-operate to regulate the stability of the U11-48K pre-mRNA. RNA 19, 380-389.
Pessa, H.K.J., and Frilander, M.J. (2011). Minor splicing, disrupted. Science 332, 184-185.
Verbeeren, J., Niemelä, E.H., Turunen, J.J., Will, C.L., Ravantti, J.J., Lührmann, R., and Frilander, M.J. (2010). An ancient mechanism for splicing control: U11 snRNP as an activator of alternative splicing. Mol Cell 37, 821-833

Postdoctoral Position Available from Spring 2015 in the Yap Lab

A postdoctoral position is available from Spring 2015 in the Yap Lab (biochem.slu.edu/faculty/yap) at the Edward A. Doisy Department of Biochemistry and Molecular Biology at Saint Louis University School of Medicine. The research project will focus on the mechanism by which ribosome undergoes translational stalling in response to ribosomal antibiotics and arrest peptides. A variety of experimental methods will be employed, including genome-wide sequencing, molecular genetics and fluorescence-based biophysical and biochemical analyses.

The candidate must have a Ph.D. in Microbiology, Biochemistry, Bioinformatics, or related field from an accredited college or university. The ideal candidate also must have a deep interest and demonstrated capability in microbial genetics and biochemistry.

Please apply online at https://jobs.slu.edu(Requisition number 20140877) or send your CV and the names and contact of three referees to Frances at [email protected].