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    BACKGROUND

    The Department of Statistics and Biostatistics and the Center for Integrative Proteomics Research at Rutgers, The State University of New Jersey seek to hire an outstanding faculty member with strong research and teaching interests in statistical analyses of biological and biomedical information.

    RESPONSIBILITIES

    Responsibilities of the position include: teaching and academic advising of both undergraduate and graduate students in statistics, biostatistics or proteomics, and conducting original research. Pursuit of external research funding is expected.

    REQUIREMENTS

    Applicants must have Ph.D. in Statistics or related fields, and also a proven track record in research at the interface between advanced analytics and the biological/biomedical sciences.

    PREFERENCES

    The search is open to all faculty ranks, including tenure-track Assistant Professor, tenure-track Associate Professor, tenured Associate Professor, and tenured Full Professor.

    TERMS

    The tenure line falls within the Department of Statistics and Biostatistics in the School of Arts and Sciences-New Brunswick Campus.

    LOCALE

    The Center is a newly built 75,000-square-foot facility dedicated to fostering interdisciplinary research in the biological and biomedical sciences using complementary quantitative tools of measurement and analysis. The Center is the home of the Institute for Quantitative Biomedicine at Rutgers and the RCSB Protein Data Bank. More information about our programs can be found in the websites: www.stat.rutgers.edu; www.proteomics.rutgers.edu; iqb.rutgers.edu; rcsb.org.

    COMPENSATION

    The Department of Statistics & Biostatistics and the Proteomics Center have strong ties. Together they will provide access to a broad array of excellent research facilities and a competitive start-up package.

    HOW TO APPLY

    Interested individuals should apply online through the Rutgers Interfolio website link (apply.interfolio.com/36128) by providing a curriculum vitae, research summary, current research support, and teaching statement, and arranging for submission of at least three confidential letters of reference.

    DEADLINE

    Review of applications is expected to conclude in December 2016.

    POLICY

    Rutgers, the State University of New Jersey, is an Equal Opportunity / Affirmative Action Employer. Qualified applicants will be considered for employment without regard to race, creed, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability status, genetic information, protected veteran status, military service or any other category protected by law. As an institution, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

    BACKGROUND

    The Department of Entomology and Plant Pathology, University of Tennessee Institute of Agriculture is seeking a postdoctoral associate to participate in an NSF-funded project to build new cyberinfrastructure for tree genomic and genetic data, including expanding the existing Hardwood Genomics database (hardwoodgenomics.org) and integration with TreeTaggr, a citizen science outreach effort (www.treetaggr.info). The project requires integration of datatypes such as genotypes, phenotypes and GIS coordinates. Development of new web modules will be within the Tripal software framework (tripal.info), which is based on Drupal content management system. The position will encompass activities such as writing PHP and javascript code, developing HTML and CSS templates, integrating biological and genomic data into databases, and building the user interface systems for scientists to view, download, search and manipulate data. The job will require teamwork with biologists and computer scientists as well as the ability to work independently. The successful applicant will be exposed to interdisciplinary, cutting edge research in the field of bioinformatics and will have the opportunity to expand their skill set and grow with this exciting field of science.

    RESPONSIBILITIES

    • Design and build new php-based Tripal modules that meet Drupal and Tripal coding standards, and that allow upload, searching and display of genomic data types
    • Use web services to transfer data between websites
    • Use a mapping platform such as the Google Maps API to build an interactive online map of tree locations and associated data
    • Install and improve existing Tripal modules to load large datasets and display results to users
    • Contribute to the writing of scholarly publications

    REQUIREMENTS

    • PhD in bioinformatics, computer science, molecular biology and/or the life sciences.
    • Proficient in a Linux operating system environment with minimal systems support
    • Demonstrated experience in PHP, Java or other programming language
    • Experience with a database platform such as MySQL or PostgreSQL.
    • Excellent communication and problem-solving skills.
    • Ability to interact with scientists from diverse disciplines and backgrounds.
    • Ability to work independently and to prioritize and manage a variety of tasks.

    PREFERENCES

    • Experience in web site development.
    • Experience in software development.
    • Familiarity with web programming, particularly development of Drupal code modules
    • Demonstrated experience in developing PHP code
    • Familiarity with bioinformatics data sets such as genes, genomes, genetic maps, etc.
    • Experience with using web-based map platforms such as the Google Maps API

    TERMS

    Regular full time position with benefits

    LOCALE

    The University of Tennessee, Knoxville Institute of Agriculture, AgResearch

    COMPENSATION

    $50k based on qualifications and experience

    HOW TO APPLY

    Required documents to apply: CV, transcripts, 2 professional references (upload as one PDF or DOC file)

    Please apply online at ut.taleo.net/care[...]0011F

    Questions may directed to mstaton1 at utk dot edu, but applications will only be accepted via the University of Tennessee online application system.

    DEADLINE

    Open until filled.

    POLICY

    EEO/AA Statement /Non-Discrimination Statement:
    The University of Tennessee is an EEO/AA/Title VI/Title IX/Section 504/ADA/ADEA institution in the provision of its education and employment programs and services. All qualified applicants will receive equal consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity, age, physical or mental disability, or covered veteran status.

    Inquiries and charges of violation of Title VI (race, color, national origin), Title IX (sex), Section 504 (disability), ADA (disability), ADEA (age), sexual orientation, or veteran status should be directed to the Office of Equity and Diversity (OED), 1840 Melrose Avenue, Knoxville, TN 37996-3560, telephone (865) 974-2498 (V/TTY available) or 974-2440. Requests for accommodation of a disability should be directed to the ADA Coordinator at the Office of Equity and Diversity.

    BACKGROUND

    The Department of Entomology and Plant Pathology, University of Tennessee Institute of Agriculture is seeking a web developer and systems administrator. The applicant will participate in an NSF-funded project to expand a database and website for plant genetic and genomic data. The project requires administration of web servers and development of new web modules in the Drupal CMS. The position will encompass activities such as writing PHP and javascript code, developing HTML and CSS templates, integrating biological and genomic data into databases, and building the user interface systems for scientists to view, download, search and manipulate data. The job will require teamwork with biologists and computer scientists as well as the ability to work independently. The successful applicant will be exposed to interdisciplinary, cutting edge research in the field of bioinformatics and will have the opportunity to expand their skill set and grow with this exciting field of science.

    RESPONSIBILITIES

    • Administer both the software and hardware for live and development Apache web servers, including data backups
    • Install and improve existing Tripal modules to load large datasets and display results to users
    • Design and build new php-based Tripal modules that meet Drupal coding standards, and that allow upload, searching and display of genomic data types
    • Develop basic competency in genomics and bioinformatics in order to propose and implement new concepts and technical solutions for the web site(s)
    • Contribute to the writing of scholarly publications

    REQUIREMENTS

    • BS in bioinformatics, computer science and/or the life sciences or equivalent experience. (Graduate work in bioinformatics may be pursued during this work in the EPP MS program or EPPN PhD program for qualified applicants)
    • Proficient in a Linux operating system environment with minimal systems support
    • Demonstrated experience in PHP, Java or other programming language
    • Experience with a database platform such as MySQL or PostgreSQL.
    • Excellent communication and problem-solving skills.
    • Ability to interact with scientists from diverse disciplines and backgrounds.
    • Ability to work independently and to prioritize and manage a variety of tasks.

    PREFERENCES

    • Experience in web site development.
    • Experience in software development.
    • Familiarity with web programming, particularly development of Drupal code modules
    • Demonstrated experience in developing PHP code
    • Familiarity with bioinformatics data sets such as genes, genomes, genetic maps, etc.
    • Experience with building and administering an Apache web server

    TERMS

    Regular full time position with benefits

    LOCALE

    The University of Tennessee, Knoxville Institute of Agriculture, AgResearch

    COMPENSATION

    $47-50k based on qualifications and experience; Pay grade 39

    HOW TO APPLY

    Required documents to apply: CV, transcripts, 2 professional references (upload as one PDF or DOC file).

    To apply, please visit ut.taleo.net/care[...]0011G

    Questions about the position may be directed to mstaton1 at utk dot edu, but applications will only be accepted through the University of Tennessee application system.

    DEADLINE

    Open until filled.

    POLICY

    EEO/AA Statement /Non-Discrimination Statement:
    The University of Tennessee is an EEO/AA/Title VI/Title IX/Section 504/ADA/ADEA institution in the provision of its education and employment programs and services. All qualified applicants will receive equal consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity, age, physical or mental disability, or covered veteran status.

    Inquiries and charges of violation of Title VI (race, color, national origin), Title IX (sex), Section 504 (disability), ADA (disability), ADEA (age), sexual orientation, or veteran status should be directed to the Office of Equity and Diversity (OED), 1840 Melrose Avenue, Knoxville, TN 37996-3560, telephone (865) 974-2498 (V/TTY available) or 974-2440. Requests for accommodation of a disability should be directed to the ADA Coordinator at the Office of Equity and Diversity.

    Submitter

    BACKGROUND

    SRA International, a leader in providing professional bioinformatics services to the Federal Government, is recruiting multiple bioinformatics professionals for potential contract work at the NIH in Rockville, MD.

    RESPONSIBILITIES

    Bioinformatics Data Analysis:
    • Provide analysis, consultation, and training services for data analysis, technical and scientific training and support for analyses and tools for variant analysis, annotation, function prediction, transcript profiling, and pathway and network analysis.
    • Provide expertise on informatics software and tool development as the liaison between the researchers and the software development team to identify requirements, develop use cases, and identify analysis tools to meet the requirements and provide outreach for these products to researchers
    • Develop pipelines to automate analysis, including use of HPC environments
    • Provide molecular modeling, docking, and simulation informatics services to address structural biology questions involving both small molecules (cheminformatics) and macromolecules using a variety of techniques, including: modeling, folding, simulation/molecular dynamics, docking and virtual ligand screening, computational aspects of empirical structure determination techniques (e.g. X-ray crystallography, NMR spectroscopy), and visualization.
    • Provide evolutionary biology informatics services to compute evolutionary relationships of sequence data that can be used to understand the origins of pandemics, antimicrobial resistance, immune responses.
    • Develop and deliver training seminars in biomedical informatics-related topics
    • Prefer familiarity with cloud infrastructure for computing and market analysis of bioinformatics software
    • Familiarity with latest experimental techniques used in biomedical research and current tools for such analysis
    Bioinformatics Software Development:
    • Design, develop, test, and document analysis pipelines, biomedical tools, and databases to store, analyze, interpret, and visualize biomedical data using primarily open-source algorithms/software packages on distributed computing environments; provide support of these to end users.
    • Create new and use existing algorithms and robust and secure software systems for bioinformatics, including composing, editing, and compiling open-source code
    • Work within HPC environments and apply solutions to reduce bottlenecks associated with storage and management of data.
    • Experience with machine learning, cloud computing, and data visualization
    • Ability to work with open source as well as COTS software
    • Support full lifecycle administration development and customization for in-house-developed (and COTS (currently LabWare) LIMS.

    REQUIREMENTS

    Bioinformatics Analysts:
    • Education and Experience – Ph.D. in life sciences with 2+ years/ MS in life sciences with 5+ years providing analysis, consultation and training services in biomedical informatics services in omics related to allergy, immunology and infectious disease research with demonstrated publication record of 3+ papers in bioinformatics within the last 4 years and experience in presenting results and supporting outreach
    Bioinformatics Developers:
    • Education and Experience – Background in bioinformatics, biology or related science with related publication(s) demonstrating the use or development of computational biology/bioinformatics/big-data/data science applications; B.S. (or other graduate degree with equivalent experience) in computer science, data science, or informatics and 3+ years of experience working with biomedical scientific data, including large-scale data and distributed storage/computing systems. At least 3 years of recent experience developing pipeline processing scripts or developing web applications with the following technologies/frameworks and software in an Agile Scrum environment:
      • Perl, Python, Bash Shell, HTML, CSS, XML, JSON, JavaScript; Java EE and JSP or PHP
      • Git and Github
      • Docker and/or other container packages; development of RESTful APIs
      • Apache and Apache Tomcat
      • Hibernate or related frameworks
      • Angular, Bootstrap, or Google Web Toolkit web development frameworks
      • MySQL or other relational database management systems
      • HPC computing environments with DRM systems such as SGE/OGE or Torque
      • Linux or Unix-based operating system
    Additional Desired Skills for All Positions:
    • Strong interpersonal, presentation, written, and oral communication skills to convey bioinformatics principles and concepts to non-specialists clearly, and advise on relevant software and tools
    • Attention to detail, including time and project management skills, to document, track, update, and generate reports on ongoing projects
    • Ability to work both independently and as part of an in-person and remote multi-disciplinary team with a high level of personal and professional drive and initiative

    LOCALE

    Rockville, Maryland, USA

    HOW TO APPLY

    Requisition number 2016-9294 on jobs.csra.com

    DEADLINE

    August 5, 2016

    BACKGROUND

    The Computational Biology Program at Oregon Health and Science University (OHSU), Portland, OR is committed to leading the development of next-generation patient care through discoveries made by big data analytics, enabled by values of open access data, open source code, highly collaborative team science, and professional software engineering methodologies.

    Critical to achieving this mission, as a software developer, you will specialize in genomic, imaging, and clinical analysis applications, leveraging your talents to change the world in the fight against disease. You are: passionate about open-source software and transparent sharing of information, enthusiastic about working in a team that finds quantitative insights in complex data and develops interactive tools to enable clinicians and researchers to understand cancer, experienced in thinking analytically and developing software tool and an organized self-starter who enjoys creative freedom in solving computational challenges.

    RESPONSIBILITIES

    • Develop and extend analytics and data management applications to facilitate management and analysis of genomics, clinical, and imaging data.
    • Establish and maintain standards for structured software & systems engineering, including requirements, design, code, test, quality, configuration & release management and project management.
    • Provide documentation and user support allowing computational researchers across campus to access and re-use analysis tools.
    • Maintain well-curated, highly structured, transparent omics, imaging, or clinical data resources.
    • Develop tools to integrate commonly used open source bioinformatics software applications.
    • Participate in leading international efforts aimed at establishing best practices and standards for genomic data representation and analysis.

    REQUIRED

    • Advanced skills in multiple high level programming languages, preferably Python, JavaScript, Java, Scala, or R.
    • Experience in professional software development techniques.
    • Bug and issue tracking systems.
    • Distributed source code management systems.
    • Strong ability to initiate and collaboratively drive projects as a dedicated and passionate member of a diverse non-hierarchical team.
    • Critical thinker, with willingness and ability to learn new subject areas.
    • Ability to effectively translate and convey expertise across domains.
    • Excellent communication, analytical and organizational skills, both written and verbal.
    • Collaborative approach to resolving problems.

    PREFERENCES

    • 7+ years of full-time development experience.
    • Computing experience in a Unix/Linux environment.
    • Experience in a professional, team-oriented software development environment.
    • A passion for developing web services for science applications, including:
    • Distributed workflow execution and data processing
    • UI design for data exploration and visualization
    • Hands-on DevOps experience for scientific computing environments

    TERMS

    Full-time

    LOCALE

    Portland, Oregon

    HOW TO APPLY

    Please visit www.ohsu.edu/xd/a[...]rces/

    Search for Jobs > Keyword search > IRC52148

    BACKGROUND

    OHSU is ranked as one of the nation's top biomedical institutions in patient care, research, and education, with an annual operating budget of over $2.3 billion, over $340 million in annual grant funding, over 4,000 students and trainees, and nearly 1 million patient visits per year. Multiple departments rank among the top 5 in annual grant funding, including neuroscience, microbiology, ophthalmology, otolaryngology, and emergency medicine. OHSU is one of the nation's fastest growing biomedical institutions, bolstered by long-term resource commitments, such as the $1 billion Phil and Penny Knight "challenge" to support research in OHSU's Knight Cancer Institute, led by Dr. Brian Druker, who pioneered the concept of gene targeted therapy by demonstrating the efficacy of the revolutionary cancer drug Gleevec in chronic myelogenous leukemia. OHSU provides substantial resources to enable data intensive science, including a world-class exascale supercomputing cluster, close interactions and resource commitments by leading technology companies such as Intel, tight integration with clinical and basic research programs across campus, graduate training programs in quantitative biosciences, biostatistics, biomedical informatics, bioinformatics and computational biology, and substantial long-term resource commitments, including the $1 billion Phil and Penny Knight "challenge" to support cancer research, with a significant focus on computation. The Computational Biology Program at Oregon Health and Science University (OHSU), Portland, OR is committed to leading the development of next-generation patient care through discoveries made by big data analytics, enabled by values of open access data, open source code, highly collaborative team science, and professional software engineering methodologies.

    RESPONSIBILITIES

    We are seeking a skilled scientific programmer to develop genomic, imaging, and clinical analysis applications on a distributed data / workflow management and analytics platform currently under development. This position will work in a team oriented software development environment, following best practices such as code sharing through GitHub and development of structured software APIs. A successful candidate will contribute to the international development of standardized APIs and data schemas, and develop implementations compatible with such APIs, ensuring that the system is interoperable within the emerging community ecosystem of software tools.
    • Develop custom analytics and data management applications to facilitate one or more of the following: large-scale genomic data analysis; machine learning methods to infer genotype-to-phenotype predictive models; analysis of quantitative imaging data.
    • Work with the platform development team to implement scalable cloud-enabled workflows to disseminate analytical advances to the research community.
    • Establish and maintain standards for structured software & systems engineering, including requirements, design, code, test, quality, configuration & release management and project management.
    • Provide documentation and user support allowing computational researchers across campus to access and re-use analysis tools.
    • Maintain well-curated, highly structured, transparent omics, imaging, or clinical data resources.
    • Develop tools to integrate commonly used open source bioinformatics software applications.
    • Participate in leading international efforts aimed at establishing best practices and standards for genomic data representation and analysis.

    REQUIREMENTS

    • Advanced skills in a high level programming language, preferably Python, R, or Java
    • Experience in one of the following:
      • Analyzing next-generation DNA or RNA sequencing data
      • Advanced machine learning or statistical techniques, such as probabilistic graphical models, Bayesian inference, and optimization methods
      • Image processing algorithms and biomedical image analysis workflows
    • Experience using structured engineering methods for specifying, designing, and implementing systems
    • Experience with architecture and tools for managing "omics" or imaging data
    • Ability to prioritize multiple tasks at one time
    • Excellent communication, analytical and organizational skills, both written and verbal
    • Ability to work independently and as part of a team while being collaborative in resolving problems
    • A desire to change the world and contribute to the elimination of human disease

    TERMS

    Full-Time

    LOCALE

    Portland, Oregon

    COMPENSATION

    We offer highly competitive recruitment packages, comprehensive benefits, and a rewarding work and life environment. OHSU is located in Portland, Oregon – a city whose breathtaking scenery, exciting location, mild weather, and friendly people have all contributed to its appearance on numerous "Best Of" lists, including Online Insider's "Top 10 Least Expensive Cities", Money Magazine's "Top 10 Places to Vacation" and "Top 10 Best Places to Live", and American Style Magazine's "Top 25 Arts Destinations".

    HOW TO APPLY

    Please visit www.ohsu.edu/xd/a[...]rces/

    Reference: IRC46014

    Review of applications will begin immediately, and will remain open until positions are filled. All applications will be reviewed for multiple open computational biology positions at OHSU, as announced in several job postings. Applications should include a CV and cover letter. We encourage including the following in the cover letter: Please indicate if you have seen any other job postings at OHSU that you would like to be considered for. It is not necessary to apply multiple times. Provide links to open source code (e.g. through GitHub or other code repository) that you are most proud of and describe the relevance to advancing one of the research areas. Describe in 1 or more paragraphs how your personal philosophy or career goals relate to the values of team-oriented science, with examples of how you have embodied these values in your career.

    POLICY

    OHSU is an equal opportunity, affirmative action institution. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of disability or protected veteran status. Applicants with disabilities can request reasonable accommodation by contacting the Affirmative Action and Equal Opportunity Department at 503-494-5148.

    Submitter

    BACKGROUND

    CSRA is seeking a mid-level or junior Bioinformatics Scientist to join our teams in Atlanta supporting the CDC, National Center for Immunizations and Respiratory Diseases (NCIRD). This individual will support and assists multiple stakeholders in the development, implementation, and administration of computational systems and tools to meet the Division's growing demands on Next Generation Sequencing (NGS) technologies. In this role you will work with diverse team members, including linux and High Performance Computing (HPC) administrators as well as bioinformatics scientists, to develop and implement tools to translate NGS results into meaningful biological insights using contemporary methods including variant analysis, comparative genomics, statistical modelling, phylogenetic methods, and integration with other information types. To be successful in this role, you should be able to interface between the bioinformatics scientists and Linux system administrators to ensure continuous support of NGS bioinformatics applications within multiple laboratories of NCIRD. The ideal candidate will be a skilled bioinformatics professional with a strong linux background who possesses a proactive and engaging attitude, strong communication skills, and the desire to work in a dynamic, high-priority environment.

    In this role, you will be a member of a small team of skilled bioinformatics scientists and laboratory scientists focused on leveraging NGS capabilities to develop the next generation of surveillance and laboratory diagnostic tools used in the global fight against disease. Position is for full time employment with CSRA and will be based onsite at the CDC campus off Clifton Rd.

    RESPONSIBILITIES

    Key responsibilities will involve performing on a small team the following:
    • Support the development of cutting-edge pipelines and data management systems for the analysis and interpretation of NGS data including NGS data processing, metagenomics, comparative genomics, variant calling, annotation, interpretation, and data presentation
    • Participate in the technical development process of an emerging NGS analytics and surveillance platforms
    • Implement state-of-the-art computational methods, and assist in the development of innovative approaches to software challenges that touch all aspects of NGS data analysis and management
    • Develop software pipelines in iterative cycles in a timely manner, based on schedules developed in collaboration with the project manager and other team members
    • Conduct programming and/or scripting using languages such as Python, Perl, Bash, and/or Java
    • Provide expertise in algorithm generation as well as statistical and computational methods for the analysis of complex, high-throughput biological data
    • Analyze large-scale genomic datasets acquired internally and through collaboration with other public health organizations worldwide, using statistical/mathematical packages such as SAS, R, and/or MATLAB
    • Maintain expertise in the science and application of genomic technologies
    • Develop documentations and assist in providing professional grade reports on ongoing sequencing, analysis, and surveillance activities
    • Report on project and task progress through daily verbal and monthly written communications
    • Help to ensure that software adheres to appropriate government and regulatory compliance requirements
    • Work with other team members to mature and integrate analytical tools/pipelines into user accessible tools/interfaces in UNIX/Linux and high performance computing environments
    • Serve as a junior or mid-level subject matter expert to guide complex software development activities

    REQUIREMENTS

    • M.S. in biology, computational biology, biostatistics, or related fields, and 2+ years' experience (or equivalent combination of education and experience, such as PhD and 1+ year)
    • 1+ years' professional experience in bioinformatics & Next Generation Sequencing (NGS) data analysis
    • Demonstrated fluency in UNIX/Linux computing environments
    • Demonstrated programming and/or scripting experience in one or more languages such as Python (preferred), Perl, Bash, and/or Java
    • Experience in pipeline generation and/or computational methods implementation
    • Excellent written and verbal communications skills, and proven ability to interact productively in a scientific team environment

    PREFERENCES

    • Ph.D. in Bioinformatics, Biostatistics, or Computational Biology or other relevant discipline preferred
    • Experience with High Performance Computing environments is preferred
    • Experience with standard/common tools for NGS data analysis including SAMtools, aligners (BWA, Bowtie2, etc.), de novo assemblers (SPAdes, Velvet, SOAP de novo, CLC, Geneious, etc.), and various BLAST methods is preferred
    • Experience with MEAN (MongoDB, Express.js, Angular.js, Node.js)
    • Experience with developing database applications using PostgreSQL, MySQL, and/or NoSQL
    • Strong in statistical/ mathematical packages such as SAS/R/MATLAB
    • Comfortable working in a dynamic, fast paced environment
    • Experience with multiple Next Generation Sequencing (NGS) technologies such as Illumina, IonTorrent, PacBio, and Oxford Nanopore
    • Experience working with code repository/version control systems

    TERMS

    Full time employment

    LOCALE

    Atlanta, GA

    COMPENSATION

    Negotiable

    HOW TO APPLY

    Please apply directly online via www.csra.com to job #9196 or via this link jobs.csra.com/job/[...]86796

    DEADLINE

    August 30th, 2016

    POLICY

    EEO

    BACKGROUND

    Description:
    Group Leader, Platform Bioinformatics

    Main Function:
    The group leader will direct a new bioinformatics group in the MSKCC Center for Molecular Oncology, a program developed to lead large-scale translational and clinical research and promote "precision" medicine through tumor molecular profiling. He/she will supervise a group of engineers, programmers and computational scientists to develop and utilize software and database systems to track and manage laboratory processes, catalyze technology development, and analyze "next-generation" sequence data primarily from human tumors. He/she will work closely with CMO leadership, experimental and computational biologists, and technical staff in the Center. He/she will also assist clinical and translational researchers with analysis of core genomic projects.

    REQUIREMENTS

    Knowledge Required:
    Highly organized and self-directed individual to work in a dynamic, team-oriented environment. MS degree required, PhD degree strongly desired in bioinformatics, computer science, genomics, or relevant field. At least 7-10 years of postgraduate training in academic or industry research is required with expertise operating in a high-throughput production environment. Cross-disciplinary and strong analytic skills, as well as broad experience with bioinformatics methods, databases, software, and computer programming languages are essential. Previous managerial experience of a multifaceted group is mandatory.

    Qualifications:
    Thorough experience with the following is required:
    • UNIX environment
    • Next-generation sequence analysis packages (e.g. Picard, Samtools, GATK)
    • Advanced programming skills
    • Database management (e.g., both SQL and modern noSQL systems)
    • Statistical packages (e.g., R)
    • High performance computing
    Essential Skills:
    • Outstanding commutation and interpersonal skills
    • Detailed expertise and proven track record with bioinformatics concepts, methods, and tools
    • Strong organizational and troubleshooting abilities
    • Familiarity with genomic technologies
    • Proficiency with genomic data, tools, and databases
    • Experience with human cancer bioinformatics analysis desired
    • Demonstrated attention to detail and analytical skills
    • Excellent time management skills, especially involved the simultaneous management of multiple projects
    • Experience in software management strongly desired
    • Leadership skills and ability to work well in a team environment
    • Passion for science and desire to impact cancer

    TERMS

    Duration: Full Time

    HOW TO APPLY

    Via website and email bic-recruit[at]cbio.mskcc.org. Please include #BGL2016 in the subject line.

    Url: bit.ly/24MKMPj

    BACKGROUND

    Description: The mission of the Marie-Josée and Henry R. Kravis Center for Molecular Oncology is to promote "precision" oncology through the expansion of genomic analysis for the diagnosis and treatment of cancer patients. The CMO strives to cultivate an environment of team science by bringing together scientists and clinicians with diverse expertise who are committed to translating novel molecular insights into maximal clinical benefit.

    RESPONSIBILITIES

    As a Bioinformatics Engineer, you will be involved in the design, development and maintenance of computational pipelines in the center. This will involve end-to-end processing that integrates existing tools as well as development of custom methods for data mining, annotation and analytics. To be successful you should have advanced programming skills, in particular significant knowledge of parallel computing techniques and experience with good coding practices and software design.

    In this role you will work with computational and experimental biologists in a dynamic and exciting academic environment at the nexus of cancer biology, computer science, statistics and clinical research.

    REQUIREMENTS

    • Bachelors in a quantitative field of study
    • Masters in Computer Science, Bioinformatics or related quantitative discipline
    • Parallel/High-performance computing experience
    • Advanced skills in Perl or Python
    • Experience in software engineering tools and methods

    PREFERENCES

    • Experience in Bioinformatics software development
    • Prior work with next-generation analysis toolkits (PICARD, GATK, samtools, etc.)
    • R/Bioconductor experience
    • C/C++, Java programming
    • Relational databases (e.g. Oracle, MySQL) and/or modern noSQL database systems

    TERMS

    Duration: Full Time

    HOW TO APPLY

    Via website and email bic-recruit[at]cbio.mskcc.org. Please include #BSE2016 in the subject line.

    Url: bit.ly/298HJh1

    BACKGROUND

    Description: The mission of the Center for Molecular Oncology (CMO) is to promote precision oncology through genomic analysis to guide the diagnosis and treatment of cancer patients. The CMO brings together clinicians and scientists throughout MSKCC to conduct large-scale translational research involving molecular characterization of patient tumor specimens in order to identify correlations between genomic features and clinical outcomes.

    RESPONSIBILITIES

    As a Computational Biologist / Bioinformatics Analyst you will:
    • Provide bioinformatics support in the development of next-generation sequencing applications to characterize the spectrum and clinical significance of genetic mutations in human tumors.
    • Develop new and utilize existing software and database systems to track experimental parameters, catalyze technology development, and analyze next-generation sequence data.
    • Work with experimental and computational biologists, clinical and translational research collaborators, and scientists in the MSKCC Center for Molecular Oncology.
    • Design, develop, and operate computational pipelines for the analysis of next-generation sequencing data.
    • Analyze data sets to discover and annotate cancer-causing genetic mutations in tumor specimens.
    • Evaluate performance of novel technology platforms and assays.
    • Work directly with research groups to analyze biomedical data and address scientific problems with bioinformatics techniques and tools and train researchers in the use of computational and bioinformatics tools
    • Develop, refine, and improve bioinformatics tools for interpretation of large genomic data sets.
    • Evaluate and test third party software packages.
    • Track specimen information, experimental and analysis parameters, performance metrics, and genomic results in databases
    • Manage and archive large data sets from next-generation sequencing experiments
    • Participate in the establishment and maintenance of a Laboratory Information Management System (LIMS)
    • Install and maintain software and data
    • Maintain detailed records of all analyses
    • Present results and progress updates at lab meetings and make presentations to experimental and scientific collaborators
    • Attend seminars, lectures, and training courses to learn new computational biology skills to remain up to date with the cancer genomics field and learn new programming languages or techniques as necessary.

    REQUIREMENTS

    You are:
    • A detail-oriented, effective communicator with an ability to build strong relationships
    • An excellent problem-solver with the ability to analyze situations, draw conclusions, make recommendations and convey this information in a timely and proficient manner
    • Passionate about science and have a desire to impact cancer. May lead and direct the work of others
    You have:
    • Master's degree or equivalent with 2-4 years of Bioinformatics software and system development required.
    • Cross-disciplinary and strong analytic skills, as well as broad experience with bioinformatics methods, databases, software, and computer programming languages are essential.

    TERMS

    Duration: Full Time

    HOW TO APPLY

    Via website and email bic-recruit[at]cbio.mskcc.org. Please include #CB2016 in the subject line.

    URL: bit.ly/29gsLH5

    BACKGROUND

    A postdoctoral position is available in Computational Systems Biology Group in the Department of Biological Sciences and the Center for Computation & Technology at Louisiana State University in Baton Rouge. The major focus of our group is the design and development of novel algorithms for the modeling and analysis of biological networks. We are interested in applying various tools from different research areas such as Structural Bioinformatics, Functional Genomics, Cheminformatics and Pharmacogenomics to study the evolution and organization of pathways into biological networks with the primary application in modern drug discovery and design.

    For more information visit: brylinski.cct.lsu.edu

    REQUIREMENTS

    Candidates should have a PhD degree in Computational Chemistry/Biology, Computer Science, Bioinformatics or a related discipline, a genuine interest in interdisciplinary work and a track record of publications in leading peer-reviewed journals. A solid knowledge of Linux, extensive experience in high-performance computing, programming in C/C++, Perl, Python, Java, etc. and excellent communication skills are highly desired. The candidate is expected to collaborate with graduate students, postdocs and research groups at LSU as well as other institutions.

    LOCALE

    Baton Rouge, Louisiana, USA

    HOW TO APPLY

    Qualified applicants should send a cover letter, CV, publication list and contact details of at least three referees by email to Dr. Michal Brylinski at michal[at]brylinski.org.

    DEADLINE

    Applications will be considered until the position is filled.

    BACKGROUND

    Company Information:
    Leidos Biomedical Research, Inc. (LBRI), a wholly owned subsidiary of Leidos, operates the Frederick National Laboratory for Cancer Research (FNLCR). FNLCR is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI). It is the only FFRDC dedicated to biomedical research. Through its status as an FFRDC, FNLCR provides NCI and others with a unique national resource to accelerate the development and delivery of effective preventive, diagnostic, and therapeutic products for cancer and AIDS.

    The breadth of FNLCR's activities spans the research and development spectrum, including investigator-initiated, hypothesis-driven research into cancer and AIDS; advanced technology programs focused on genetics and genomics, proteins and proteomics, imaging, nanotechnology, bioinformatics, and laboratory animal sciences; clinical operations in support of NCI and National Institute of Allergy and Infectious Diseases (NIAID)-sponsored clinical trials, as well as NCI drug discovery and development efforts; and management and operations of biopharmaceutical development and manufacturing programs under current Good Manufacturing Practice conditions for NCI and NIAID. Administrative, procurement, financial, safety, and facilities support is provided to these R&D activities through state-of-the-art business processes. LBRI has approximately 1,900 employees and manages an annual operating budget of approximately $450M.

    For more information about Leidos Biomedical Research Inc., please visit our webpage at www.leidosbiomed.com.

    RESPONSIBILITIES

    Program Description:
    The Molecular Characterization Laboratory (MoCha) is part of Leidos Biomedical Research's Clinical Research Directorate (CRD) at the Frederick National Laboratory for Cancer Research. The MoCha Laboratory is responsible for providing high-level research in support of the NCI-Cancer Diagnostics Program (CDP) within the Division of Cancer Treatment and Diagnosis (DCTD). MoCha is charged with the development and application of genomic assays for use in medical research and diagnostics for DCTD-sponsored national extramural clinical trials.

    The Molecular Characterization Laboratory (MoCha) focuses on development and application of novel genomic assays for clinical applications.

    Job Description:
    The Bioinformatics Analyst II will: 1) be responsible for providing substantial bioinformatics support for the MoCha clinical laboratory, including the analysis and interpretation of high throughput genomic data, 2) provide expertise in the biological interpretation of results, including mutation impact assessment, expression analysis, statistics support and prioritization of identified loci/genes lists, classification model building and determining correlation with clinical data derived from patients, 3) interact with investigators throughout the entire experimental process from study design to result interpretation including manuscript preparation, 4) provide support to lab staff in the application of basic data analysis and study design, 5) provide bioinformatics knowledge as a shared team resource, 6) maintain and track complex data for multiple projects, 7) work with lab managers to update genetic information in databases, 8) work closely with clinical lab staff to provide computation resources and to support data analysis and storage, and 9) coordinate and integrate software applications and databases within the larger group including the Bethesda, Frederick, and Shady Grove NCI campuses.

    REQUIREMENTS

    Basic Qualifications:
    • Possession of a Bachelor's degree from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) in biomedical science/bioinformatics/math/statistics/computer related field or four (4) years related experience in lieu of degree
    • Foreign degrees must be evaluated for U.S. equivalency
    • A minimum of two (2) years of progressively responsible relevant experience
    • Experience in next generation sequence analysis (NGS) including quality metrics, mapping, variant calling and biological interpretation
    • Experience analyzing large genomic data sets including integration with data available from public or private sources
    • Hands-on experience in data processing and analyzing sequencing, expression and other array data including quality and biological assessment
    • Proficiency in Unix (Linux) system, scripting and programming languages such as Shell, R, Python, JavaScript, Perl, Java, SQL and bioinformatics tools and database management
    • Experience performing statistical analysis of complex biological data
    • Strong organizational skills and information tracking experience for data with complex structures

    PREFERENCES

    Preferred Qualifications:
    • Peer reviewed publications demonstrating knowledge of the biology of cancer
    • Experience with Ion Torrent systems, including the Ion Reporter system
    • In-depth understanding in molecular biology techniques, oncology and clinical research
    • Experience in data integration, database construction, application development and visualization
    • Experience in porting applications to a web environment and working with workflow tools and applications
    • Excellent communication skills (written and oral)
    • Ability to work effectively in a team-oriented environment
    • Ability to identify and solve complex problems

    TERMS

    Full Time

    LOCALE

    Frederick, MD

    ABOUT US

    Leidos Overview:
    Leidos is an applied solutions company focused on markets that are seeing converging business and technological trends, and address basic, enduring human needs: defense and national security, health and life sciences, and energy, engineering and infrastructure. The Company's approximately 20,000 employees serve customers in the U.S. Department of Defense, the intelligence community, the U.S. Department of Homeland Security, other U.S. Government civil agencies and commercial health and engineering markets.

    HOW TO APPLY

    Please visit jobs.leidos.com/Show[...]NCI)/

    POLICY

    Qualified women, minorities, individuals with disabilities and protected veterans are encouraged to apply. Leidos is an Equal Opportunity Employer.

    BACKGROUND

    Company Information:
    Leidos Biomedical Research, Inc. (LBRI), a wholly owned subsidiary of Leidos, operates the Frederick National Laboratory for Cancer Research (FNLCR). FNLCR is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI). It is the only FFRDC dedicated to biomedical research. Through its status as an FFRDC, FNLCR provides NCI and others with a unique national resource to accelerate the development and delivery of effective preventive, diagnostic, and therapeutic products for cancer and AIDS.

    The breadth of FNLCR's activities spans the research and development spectrum, including investigator-initiated, hypothesis-driven research into cancer and AIDS; advanced technology programs focused on genetics and genomics, proteins and proteomics, imaging, nanotechnology, bioinformatics, and laboratory animal sciences; clinical operations in support of NCI and National Institute of Allergy and Infectious Diseases (NIAID)-sponsored clinical trials, as well as NCI drug discovery and development efforts; and management and operations of biopharmaceutical development and manufacturing programs under current Good Manufacturing Practice conditions for NCI and NIAID. Administrative, procurement, financial, safety, and facilities support is provided to these R&D activities through state-of-the-art business processes. LBRI has approximately 1,900 employees and manages an annual operating budget of approximately $450M.

    For more information about Leidos Biomedical Research Inc., please visit our webpage at www.leidos.com/abou[...]earch.

    RESPONSIBILITIES

    Program Description:
    Within the Leidos Biomedical Research Inc.'s Clinical Research Directorate, the Clinical Monitoring Research Program (CMRP) provides high-quality comprehensive and strategic operational support to the high-profile domestic and international clinical research initiatives of the National Cancer Institute (NCI), National Institute of Allergy and Infectious Diseases (NIAID), Clinical Center (CC), National Institute of Heart, Lung and Blood Institute (NHLBI), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Center for Advancing Translational Sciences (NCATS), National Institute of Neurological Disorders and Stroke (NINDS), and the National Institute of Mental Health (NIMH). Since its inception in 2001, CMRP's ability to provide rapid responses, high-quality solutions, and to recruit and retain experts with a variety of backgrounds to meet the growing research portfolios of NCI, NIAID, CC, NHLBI, NIAMS, NCATS, NINDS, and NIMH has led to the considerable expansion of the program and its repertoire of support services. CMRP's support services are strategically aligned with the program's mission to provide comprehensive, dedicated support to assist National Institutes of Health researchers in providing the highest quality of clinical research in compliance with applicable regulations and guidelines, maintaining data integrity, and protecting human subjects. For the scientific advancement of clinical research, CMRP services include comprehensive clinical trials, regulatory, pharmacovigilance, protocol navigation and development, and programmatic and project management support for facilitating the conduct of 400+ Phase I, II, and III domestic and international trials on a yearly basis. These trials investigate the prevention, diagnosis, treatment of, and therapies for cancer, influenza, HIV, and other infectious diseases and viruses such as hepatitis C, tuberculosis, malaria, and Ebola virus; heart, lung, and blood diseases and conditions; parasitic infections; rheumatic and inflammatory diseases; and rare and neglected diseases. CMRP's collaborative approach to clinical research and the expertise and dedication of staff to the continuation and success of the program's mission has contributed to improving the overall standards of public health on a global scale.

    Job Description:
    The Clinical Monitoring Research Program/Regulatory Compliance and Human Subjects Protection Program (RCHSPP) provides clinical trial management support to the National Institute of Allergy and Infectious Diseases (NIAID) Intramural Clinical Research Community, Division of Clinical Research (DCR), Office of Clinical Research Policy and Regulatory Oversight (OCRPRO).

    As part of the Protocol Navigation/Protocol Development Program (PN/PDP), the Medical Writer II: 1) writes, revises, and provides editorial assistance for clinical research protocols from concept to Institutional Review Board (IRB) submission, 2) writes compatible informed consent documents, 3) ensures protocol and informed consents meet regulatory requirements and are written in a format consistent with the guidelines set forth by NIAID; 4) works closely with the IRB to keep abreast of new guidance related to protocol and informed consent submissions for both initial reviews and amendments, and shares relevant information with PN/PDP team members, 5) collaborates with medical research scientists/Principal Investigators (PIs), Protocol Navigators (PNs), and safety, regulatory, and monitoring divisions to ensure writing deliverables are at the highest level of preparation, 6) integrates various sources of information into uniform language styles and analyzes documents for accuracy, consistency, relevancy, correctness of conclusions, alternate hypotheses, editorial corrections, and other issues for regulatory compliance, 7) collates multiple reviewers' comments, analyzes applicability, and edits documents to reviewers' satisfaction, 8) coordinates with PIs and PNs to ensure stipulations from approving bodies (e.g., scientific review, IRB, and radiation safety) are addressed appropriately and in a timely manner, 9) provides drafting and editing support as needed for other related research documents, protocol amendments, and continuing reviews, 10) performs literature reviews and background research, 11) prepares and summarizes meeting proceedings, 12) compiles scientific references and creates bibliographies using EndNote software, 13) may draft and edit Standard Operating Procedures (SOPs), meeting minutes, abstracts, manuscripts, and presentations to support the NIAID intramural research or program initiatives, 14) independently works under the general guidance of the supervisor, and 15) attends in-person meetings located at the National Institutes of Health campus in Bethesda, Maryland

    REQUIREMENTS

    Basic Qualifications:
    • Possession of a Bachelor's degree from an accredited college or university according to the Council for Higher Education Accreditation (CHEA) in biological/biomedical science or related field or 4 years related experience in lieu of degree
    • Foreign degrees must be evaluated for U.S. equivalency
    • A minimum of two (2) years' experience in a pharmaceutical, biotechnology and/or clinical environment which includes medical and/or regulatory technical writing/editing
    • Current working knowledge of the Department of Health and Human Services (DHHS) regulations, International Conference on Harmonization/Good Clinical Practices (ICH/GCP), Food and Drug Administration (FDA), and Office of Human Research Protections guidelines
    • Experience participating in the preparation of clinical documents for regulatory submissions (e.g., clinical protocols, Investigational New Drugs [INDs])
    • Ability to effectively communicate both verbally and in writing with demonstrated expertise with grammar, syntax, and format
    • Ability to write and edit clear, concise clinical documents compliant with FDA and ICH guidelines, as well as all practices and procedures related to medical writing
    • Ability to write concise meeting summaries and/or meeting minutes and create action plans
    • Ability to prioritize workload and submit high quality deliverables in a professional environment under tight deadlines
    • Ability to work in a clinical research regulatory setting, both independently and within a team, to coordinate, negotiate and facilitate the program goals
    • Strong collaborative skills with ability to build relationships within multiple groups
    • Must be detail-oriented and possess substantial organizational skills
    • Proficiency in word processing systems, i.e., Microsoft Word, MS Office, or similar systems

    PREFERENCES

    Preferred Qualifications:
    • Familiarity with therapeutic area of allergy and infectious diseases

    TERMS

    Part Time

    LOCALE

    Bethesda, MD

    ABOUT US

    Leidos Overview:
    Leidos is an applied solutions company focused on markets that are seeing converging business and technological trends, and address basic, enduring human needs: defense and national security, health and life sciences, and energy, engineering and infrastructure. The Company's approximately 20,000 employees serve customers in the U.S. Department of Defense, the intelligence community, the U.S. Department of Homeland Security, other U.S. Government civil agencies and commercial health and engineering markets.

    HOW TO APPLY

    Please visit jobs.leidos.com/Show[...]NCI)/

    POLICY

    Qualified women, minorities, individuals with disabilities and protected veterans are encouraged to apply. Leidos is an Equal Opportunity Employer.

    BACKGROUND

    Seeks an enthusiastic and experienced bioinformatics scientist who is comfortable with large data sets, rapid development and a variety of scripting languages, tools, and programming languages.

    RESPONSIBILITIES

    • Perform basic and advanced analysis on data produced from next generation sequencing systems (DNA-seq, RNA-seq, metagenomics, ChIP-seq, etc.) as well as genotyping and gene expression microarrays.
    • Develop, improve, modify, and operate data analysis pipelines.
    • Experience in de novo sequence analysis, re-sequencing, RNA-Seq
    • Develop software or use current open source software in conducting data analysis for NGS and microarray datasets at basic and advanced levels.
    • Work closely with experimental researchers to generate/provide analysis reports, project reports and perform requested custom analysis etc.

    REQUIREMENTS

    M.S. degree or Ph.D. bioinformatics, biostatistics or related field with appropriate experience in developing software or the equivalent in experience and education with 2 -5 years experience in bioinformatics

    PREFERENCES

    • Strong bioinformatics analysis/scripting experience including proficiency with a scripting language (e.g. Perl). Experience in working in a Linux/UNIX environment and experience with cluster computing is a plus.
    • Experience in software design
    • Experience with the relevant sequence analysis tools/best practices
    • Experience with setting up and analyzing Illumina platform NGS datasets; large scale data analysis and sequence assembly and annotation experience is a plus.
    • Knowledge, background, or experience in molecular biology and microbiology
    • The successful candidate will be able to prioritize and balance multiple projects to meet timelines.

    TERMS

    Three years contract

    LOCALE

    Centre of Biological Engineering, University of Minho, Braga, Portugal

    COMPENSATION

    Salary according to proven experience

    HOW TO APPLY

    E-mail to madalena.alves[at]deb.uminho.pt

    DEADLINE

    July 31, 2016

    BACKGROUND

    About Us:
    DiaTech Holdings is an emerging biotechnology company specializing in cutting edge technologies utilizing molecular based clinical assays to generate actionable data for improved patient outcomes. We are currently focused on the MiCK, CEER, and flow cytometer technology platforms for use in our clinical assay development and FDA validation studies with the primary emphasis in oncology.

    Position Overview:
    In this role, you will make significant contributions to the design and development of state of the art software applications for laboratory and analysis workflows. You will also be responsible for understanding and developing interfaces between multiple software applications that collectively support complex research and clinical workflows designed to develop and deploy predictive clinical tests in Oncology. You will be part of a dynamic and fast paced software team and will have the opportunity to work with experts in a wide range of disciplines including biology, computational sciences and translational medicine in tight knit cross-functional teams. You will be intellectually challenged and have an opportunity to participate in development of multiple predictive clinical diagnostic tests.

    RESPONSIBILITIES

    • Work closely with other software engineers, research scientists, lab staff, and computational scientists to identify and implement key automation and visualization tools.
    • Design, develop, integrate, and deploy related application components including front end development, server-side development, and system integration.
    • Provide application support for testing, debugging and applying incremental improvements in working laboratory environments, both in research and regulated environments.
    • Provide training, and troubleshooting for applications deployed to a diverse user base.
    • Comply with and help evolve process methodologies including issue tracking, source control, unit testing and coding standards.
    • Make recommendations for process improvements and new technologies that will make a positive impact on the laboratory and analysis workflow.
    • Be the point person for various computational needs that arise on pre-clinical and clinical stage projects run by cross-functional teams consisting of research biologists, instrumentation experts, biostatisticians and clinical scientists

    REQUIREMENTS

    Education/Experience:
    • A bachelor's or master's degree in computer science or related field
    • Strong programming skills using one or more of JavaScript, Python, Ruby, Java or similar languages
    • Knowledge of software engineering best practices and OO design principles
    • Experience developing full-stack web and/or Java applications
    • Experience in Java(Play), Python(Django) or Ruby(Rails) frameworks
    • Strong understanding of relational and non-relational database systems, HTML, CSS and software testing methodologies
    • Programming experience in Windows and Linux environments
    • Knowledge of biological and/or clinical data a definite plus
    • Experience in the industrial setting is a plus
    Knowledge, Skills, and Abilities:
    • Must be a self-starter
    • Ability to craft a great user experience
    • Very strong interpersonal skills and a track record of success in team-oriented environments
    • Excellent verbal and written communication skills
    • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
    • Ability to analyze complex problems
    • Ability to work after hours as needed
    • Ability and willingness to travel occasionally

    LOCALE

    San Diego, CA

    HOW TO APPLY

    Please send resume/CV with a notation of the position applying for to: careers[at]diatech-oncology.com
    OR apply on the website: www.diatechholdings.com

    POLICY

    This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization. DiaTech Holdings Inc. is an Equal; Opportunity Employer with a strong commitment to the achievement of excellence and diversity.
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