Opportunities

This page is the place to post SAS employment or training opportunities. If you know of any such opportunity, please post a comment using the form at the bottom of this page Thanks!

Note: The entries posted on this page are in ascending order chronologically, so the newest posts will be at the bottom of the page.

Responses

  1. SAS PROGRAMMING AND STATISTICIAL OPPORTUNITIES

    When you’re ready to join a company that’s as dedicated to excellence as you are, THINK THEOREM.

    Theorem Clinical Research’s Biometrics department is growing and, to reach our goals, we need more skilled, talented and dedicated SAS Programmers and Statisticians like you who are interested in exploring a new permanent home-based opportunity with a leading mid-sized CRO. Positions are open to all locations in the US and Canada, and are available immediately. For more info on those positions or to apply, follow the links below:

    Manager, SAS Programming http://tinyurl.com/mp5hmrk
    Principal SAS Programmer http://tinyurl.com/nu3nfyb
    Sr. SAS Programmer http://tinyurl.com/jwxahtv
    SAS Programmer Analyst http://tinyurl.com/ntlq2en
    Sr Principal Statistician http://tinyurl.com/mlhpsqv
    Principal Statistician http://tinyurl.com/ljv59lw

    At Theorem, you’ll join a team of like-minded individuals headed by some of the most dynamic and influential leaders in drug and medical device development today. You’ll work on cutting-edge global research projects in a fast-paced but collegial atmosphere where you’ll have the opportunity to make meaningful — and acknowledged — contributions. You’ll have opportunities to grow personally and professionally and abundant room for advancement along with generous incentive programs.

    Theorem Clinical Research Inc. is a leading midsized provider of comprehensive clinical research and development services with offices in more than 30 countries and a customer base comprised of some of the world’s top pharmaceutical, biotech and medical device companies. As a forerunner in medical device and drug-device combination trials with notable capabilities in pharmaceuticals and biologics, Theorem offers deep expertise in a broad range of therapeutic areas and in all phases of development. With some of the industry’s top scientists and most advanced clinical analytics capabilities, Theorem ensures smooth-running, successful trials. For the full-service, right-size global research partner, don’t think twice. THINK THEOREM.

    Theorem Clinical Research is an equal opportunity employer, M/F/D/V

  2. SAS PROGRAMMING AND STATISTICIAL OPPORTUNITIES
    When you’re ready to join a company that’s as dedicated to excellence as you are, THINK THEOREM.
    Theorem Clinical Research’s Biometrics department is growing and, to reach our goals, we need more skilled, talented and dedicated SAS Programmers and Statisticians like you who are interested in exploring a new permanent home-based opportunity with a leading mid-sized CRO. Positions are open to all locations in the US and Canada, and are available immediately. For more info on those positions or to apply, follow the links below:
    Manager, SAS Programming http://tinyurl.com/mp5hmrk
    Principal SAS Programmer http://tinyurl.com/nu3nfyb
    Sr. SAS Programmer http://tinyurl.com/jwxahtv
    SAS Programmer Analyst http://tinyurl.com/ntlq2en
    Sr. Principal and Sr. Analytical Statisticians http://tinyurl.com/oncjfef
    Analytical and Principal Statisticians http://tinyurl.com/oncjfef
    At Theorem, you’ll join a team of like-minded individuals headed by some of the most dynamic and influential leaders in drug and medical device development today. You’ll work on cutting-edge global research projects in a fast-paced but collegial atmosphere where you’ll have the opportunity to make meaningful — and acknowledged — contributions. You’ll have opportunities to grow personally and professionally and abundant room for advancement along with generous incentive programs.

    Theorem Clinical Research Inc. is a leading midsized provider of comprehensive clinical research and development services with offices in more than 30 countries and a customer base comprised of some of the world’s top pharmaceutical, biotech and medical device companies. As a forerunner in medical device and drug-device combination trials with notable capabilities in pharmaceuticals and biologics, Theorem offers deep expertise in a broad range of therapeutic areas and in all phases of development. With some of the industry’s top scientists and most advanced clinical analytics capabilities, Theorem ensures smooth-running, successful trials. For the full-service, right-size global research partner, don’t think twice. THINK THEOREM.
    Theorem Clinical Research is an equal opportunity employer, M/F/D/V

  3. Join us in supporting the Centers for Medicare and Medicaid as a SAS Trainer and Data Coach. Healthcare data experience required. Principals only please.

  4. Senior Biostatistician

    located in South San Francisco

    The preferred candidate will have experience in the pharmaceutical or biotechnology environment setting a high bar of excellence in the analysis and reporting of clinical study data to internal stakeholders as well as to external audiences (external experts, journals, regulators). Ideally, this experience would include exposure to the design, analysis and reporting of clinical studies in late stage clinical development.

    The senior biostatistician will support the development of innovative and efficient plans for developing new medicines in a variety of therapeutic areas.

    The Duties and Responsibilities include but are not limited to the following:

    Provides technical statistical expertise, innovation and partnership on study design and endpoint selection, calculates sample sizes and prepares the statistical section of study protocols.
    Independently develops and authors statistical analysis plans.
    Collaborates in the review of protocols, case report forms, data specifications, CSRs and other study related documents
    Performs quality control of analysis data and TFLs
    Utilizes knowledge of guidance documents to provide statistical advice, and uses knowledge of literature to provide data analysis and presentation methods to support publications and presentations.
    Ability to work on multiple clinical trials across multiple therapeutic areas.
    Proactively solicits input from others to gain common understanding and agreement.
    Plans and performs exploratory analyses of existing study data for publications, reimbursement negotiations, drug defense strategies and further development planning.
    Provides Biostatistical input into strategic decision making
    Represents the outputs of analyses with key audiences, including internal stakeholders, external experts, DSMBs, regulators and reimbursement committees
    Plays an active role in shaping late stage development programs (Phase 2B, Phase 3A, Phase 3B)

    Qualifications
    PhD degree in Biostatistics or equivalent.
    2+ years of experience in Clinical Development in a pharmaceutical or biotechnology setting in the statistical analysis of biomedical data.
    Late-stage development experience in working in teams and in interacting with key internal and external stakeholder groups, including regulatory agencies
    Working knowledge of the regulations and procedures relating to Biostatistical analysis and interpretation of late-phase development studies
    Excellent English verbal and written communication skills.
    Scientific programming capability with statistical software packages; SAS and/or R
    Detail oriented and well organized.
    Ability to work on several projects simultaneously.

    Regards,
    Julie Hilliard
    Pharmaceutical Technical Recruiter
    JGB BioPharma Consulting Inc.
    email: jhilliard@jgbbiopharma.com
    p: 650-627-7650
    See all our jobs at http://www.jgbbiopharma.com/jobs

  5. Seeking skilled Senior SAS Developers to join our Team (Direct-hire, Full-time)

    Sabre Systems is a company that promotes a work environment that encourages both personal and professional growth and a culture where each individual employee is valued and respected. We are currently seeking to fill several key technical roles supporting a Large Federal Client in Washington, DC.

    Project Overview: We are seeking Information Technology Specialists at all levels to provide the critical support in analyzing, designing, implementing and maintaining computer systems to support statistical surveys. This program helps supports operational staff performing on a number of tasks to produce timely, accurate, and relevant economic statistics develops, implements, and supports statistical application production systems, in the area of Software Development, Server/Database Administration, Network Administration, and Documentation, Requirements, and Procedures Management.

    To view full job descriptions, please go to our Careers Page:
    https://sabresystems.hua.hrsmart.com/hrsmart/ats/JobSearch/viewAll

    Consideration will be given to all candidate authorized to work in USA (US Citizens, Green Card holders and those possessing an Employment Authorization Document (EAD) or H1B transferable visa.

    These are direct-hire position with Sabre Systems, Inc. which includes medical, dental, 401K and other benefits. Salary depends on ability to meet or exceed desired employment criteria.

    We have a wide array of opportunities that I think would be of interest to you and your colleagues, but I am specifically seeking someone with your talents and expertise, so please let me know when would be a good time to contact you directly to discuss the position in more detail.

    Thank you very much for your time and consideration and I look forward to hearing from you.

    Catrina Stagnato
    Sr. Recruiter
    cstagnato@sabresystems.com

    Sabre Systems, Inc. I 2331 Mill Road, Suite 510 • Alexandria, VA 22314
    703.251.3227 (Direct) I 703.535.8120 (Office) I 703.535.8127 (Fax)

    http://www.sabresystems.com

  6. Hi All,

    James Hendrickson here – ABS Consulting is hiring. This is a great opportunity with a great company. Please see the position description below and don’t hesitate to reach out if you’re interested.

    Thanks,

    James

    ——————————————————————————————————–

    Title: Junior SAS Consultant

    Required Education: BS degree in a related field

    Clearance Requirement: Must be able to obtain a SECRET security clearance

    Job location: Metro Washington, DC area.

    General Experience: Successful candidates shall have approximately of 1-2 years of professional experience and demonstrated analytic experience with mathematics, statistics, econometrics, modeling or analytic data analysis procedures. Candidates should be proficient with Microsoft Office (Excel, Word and Powerpoint) and should have strong communication and interpersonal skills. Successful candidates should know SAS and be easy to get along with.

    Salary: $45,000 – $55,000 with comprehensive benefits.

    Special requirements: Applicants must be U.S. Citizens and eligible for a U.S. Security clearance.

    Headquartered in Houston, Texas, ABSG Consulting Inc. (ABS Consulting) is a subsidiary of ABS Group of Companies, Inc. (ABS Group) and an affiliate of ABS, one of the world’s leading Marine and Offshore classification societies founded in 1862.

    ABS has more than 2,200 employees who assist customers every day from offices located throughout the world with our major operating centers in the US, UK, Middle East, Asia-Pacific and Latin America. ABS Consulting has long been a pioneer in the areas of probabilistic risk assessment, process safety management and hazard modeling. We apply this expertise to create practical solutions to clients operating in high technical and regulated industries.

    All inquiries should be directed to James C. Hendrickson at:

    jhendrickson@absconsulting.com

    571-481-7883

  7. SAS Analytics with Oracle Database experience in Arlington, VA

    U.S. Information Technologies Corporation (USIT) is a leading provider of Oracle-based information technology solutions. Our national workforce, many of whom are former Oracle professionals, bring extensive credentials to projects needing Oracle database, development tools and e-Business suite expertise. USIT helps clients solve challenging IT problems by leveraging industry best practices and our in-depth Oracle technology expertise.

    We have a simple win-win-win philosophy. USIT offers its employees industry-leading training, benefits, and compensation plans, because we only want to attract and retain the best. You can’t hire the best unless you treat them better than anyone else will. Our consultants win because that’s what we do.

    The position will provide highly technical expertise and support in the use of RDBMS. Define file organization, indexing methods and security procedures for specific user applications. Develop, implement and maintain database backup and recovery procedures for the processing environment and ensure that data integrity, information assurance, and recoverability are built into RDBMS applications.

    Qualifications:

    4+ years of experience as a Relational Database Management System (RDBMS) Administrator in an Oracle/SAS Analytics web-based environment.
    3 years of experience in database administration management in an Oracle/SAS Analytics environment and RDMS internals.

    Preferred skills with one or more of the following

    Oracle Webfusion middleware
    Oracle 11g+ Database
    SAS Analytics
    US Citizenship required.

    Must be able to obtain a Security Clearance

    Education/Certifications

    B.A. or B.S. degree

    Secrurity+

    Sincerely,

    Lana Robbins
    Recruiter

    U.S. Information Technologies | http://www.usinfotech.com/careers.html
    4800 Westfields Boulevard | Suite 250 | Chantilly, VA
    Office: 703-543-8800 ext 197
    Toll Free: 877-USIT-USA

  8. Hi All,
    We have several SAS programmer positions open in our organization, Social & Scientific Systems, Inc. Please visit http://www.s-3.com to find out about the work we do.

    You can find details of openings at the following address.
    https://careers-s-3.icims.com/jobs/intro?hashed=-435742583&mobile=false&width=914&height=500&bga=true&needsRedirect=false&jan1offset=-300&jun1offset=-240

    Please feel free to contact me or our HR staff if you have any questions.

    Thank you,

    Devi Katikineni
    Senior Project Manager
    DKatikineni@s-3.com
    301.628.3247

    Andrew Stephens
    Human Resources
    AStephens@s-3.com
    301.628.3281

  9. Title: Load Research Analyst III

    Dominion Resources, based in Richmond, Virginia, has an exciting opportunity for an experienced SAS professional. If you possess strong analytical skills, ability to interpret data, experience with statistical tools, consider applying for this opportunity.

    At Dominion, employees are rewarded with a competitive salary and comprehensive benefits package which includes: health benefits with coverage for families and domestic partners, vacation, retirement plans, paid holidays, tuition reimbursement, and much more.

    We are looking for a Load Research Analyst III with day-to-day responsibilities including the following:
    • Design load research studies using statistical methods used in sample design, sample selection and data expansion, as well as in techniques for data collection, processing, and analysis.
    • Ability to work independently with minimal management oversight and to meet deadlines under pressure.
    • Assist Management and other corporate functions accomplish their goals by handling requests for unique load research and analysis to clarify specific problems and concerns.
    • Work with regulatory agencies to provide load research information upon request.
    • Coordinate ongoing load research studies to ensure necessary precision levels.
    • Analyze demand, energy use demographic, and other data with appropriate statistical techniques to correctly address the objectives and draw logical conclusions.
    • Report study findings and make recommendations based on findings.
    • Work with Information Technology to determine the requirements of analysis software
    Job Qualifications required for entry into this job include the following:
    • Experienced SAS user
    • Strong analytical skills. Past utility experience related to customer usage is a plus.
    • Ability to interpret data, apply appropriate analysis techniques, and present defendable findings.
    • Candidate must be customer focused, exhibit a high degree of teamwork, ability to work independently, and have attention to details.
    • Degree in Statistics, Applied Economics, Computer Science, or a related field is preferred.
    • Experience with large databases, database access, and data interpretation.
    • Experience with statistical tools/analysis, experimental design and sampling theory.
    • Understanding of SQL, UNIX, or Oracle environments.
    • Excellent presentation and communication skills.
    • Proficient in Word, Excel and PowerPoint.
    • 6+ years experience in state and/or federal regulatory and rate setting process or other equivalent analytical or quantitative experience.

    How to Apply:

    To apply for this opportunity, please visit our website at https://careers-dominion.icims.com/jobs/6371/load-research-analyst-iii/job. Other opportunities are available at http://www.dom.com/careers.

    • Is this position still open?

      • Michelle,

        I would go to the Dominion web site Dom.com and search their job board

  10. Senior Statistical Programmer

    We are seeking a seasoned Senior Statistical Programmer for a new, multi-year FSP contract with one of the world’s leading biotechnology companies. This is a key role responsible for working on the client’s systems and support various projects in their portfolio augmenting their existing staff.

    In this role you will:
    Be responsible for both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software
    Integrate data across multiple studies or drug programs
    Work with minimal supervision under the direction of a lead programmer
    Communicate issues to lead programmer or FSP technical lead
    Meet timelines or communicate proactively and effectively if timelines are at risk so that plans can be adjusted
    Attend team meetings and make yourself available during client working hours

    You have the option to work from home or be based either in our Chesterbrook, PA or Waltham, MA location.

    Qualifications and Experience
    You will have a Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc., and a minimum of five or more (5+) years of SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards.

    Additionally, we require:

    The ability to handle a moderate to large volume of complex tasks with minimal supervision
    The ability to handle ad-hoc requests with minimal guidance
    The ability to recognize when negotiating skills are needed and seeks assistance when necessary
    Excellent organizational, interpersonal, and communication skills

    Compensation & Benefits
    We offer a competitive compensation package including base, bonus, and options, as well as comprehensive medical and dental benefits and a contributing 401K plan.

    Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

  11. Statistical Programmer

    We are seeking a seasoned Statistical Programmer for a new, multi-year FSP contract with one of the world’s leading biotechnology companies. This is a key role responsible for working on the client’s systems and support various projects in their portfolio augmenting their existing staff.

    In this role you will:
    Be responsible for both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software
    Integrate data across multiple studies or drug programs
    Work with minimal supervision under the direction of a lead programmer
    Communicate issues to lead programmer or FSP technical lead
    Meet timelines or communicate proactively and effectively if timelines are at risk so that plans can be adjusted
    Attend team meetings and make yourself available during client working hours
    You will have the option to work from home or be based either in our Chesterbrook, PA or Waltham, MA location.

    Qualifications and Experience
    You will have a Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc., and a minimum of three to five (3 – 5) years of SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards.

    Additionally, we require:
    The ability to handle a moderate to large volume of complex tasks with minimal supervision
    The ability to handle ad-hoc requests with minimal guidance
    The ability to recognize when negotiating skills are needed and seeks assistance when necessary
    Excellent organizational, interpersonal, and communication skills
    Compensation & Benefits
    We offer a competitive compensation package including base, bonus, and options, as well as comprehensive medical and dental benefits and a contributing 401K plan.

    Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

  12. NONMEM Programmer

    We are seeking a NONMEM Programmer for a recently expanded five year FSP contract with a well-respected, leading biotechnology firm. This high visibility role creates input data files for NONMEM software which is used by Pharmacokinetics & Drug Metabolism (PKDM) department to conduct population PK or population PK/PD analysis. The NONMEM programmer uses SAS software to develop a program based on provided programming specifications. As an input for a SAS program, the role uses analysis data sets, either Case Report Tabulations (CRTs) or ADaMs. The NONMEM programmer also participates in the development and testing of macro utilities.

    The position can be home based or in one of our offices in Cambridge, MA; Waltham, MA; or Chesterbrook,PA.

    Qualifications and Experience
    You will have a BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject, and at least 5 years of relevant career statistical programming experience in a clinical development environment with 6 a strong preference. Additionally, we require:
    Excellent SAS data manipulation, analysis and reporting skills
    Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
    Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
    Excellent oral and written English communication skills
    Ability to provide quality output and deliverables, in adherence with challenging timelines
    Willingness and ability to learn and follow Company’s standard processes and procedures.
    Ability to work effectively on multiple tasks or projects
    Ability to lead small team projects effectively
    Ability to effectively perform complex statistical programming and related tasks
    Willingness and ability to provide guidance to team members on technical and process questions
    Working knowledge of latest CDISC SDTM, CDISC ADaM, and Define standards with strong ability to implement the standards
    Experience working with phase 1, 2, and 3 studies
    Familiarity with PK data
    Experience developing specifications for other programmers
    Compensation & Benefits
    We offer a competitive salary-based package, bonus, comprehensive medical and dental benefits, plus a contributing 401K plan.

    Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

  13. Lead SDTM Implementer

    We are seeking a Lead SDTM Implementer for a recently expanded five year FSP contract with a well-respected, leading biotechnology firm. This high visibility role will work with the CDISC Consultancy and Implementation (CCI) team, a group within the client’s Global Statistical Programming department responsible for supporting the compliant and consistent adoption of the CDISC Study Data Tabulation Model (SDTM).

    Additional responsibilities include:
    Provide support for new and ongoing studies and drive close collaboration with other CDISC Consultants and Implementers, Statistical Programmers, Global Librarians, and Data Stewardship Representatives
    Develop compliant and consistent CDISC SDTM datasets, perform CRF SDTM annotation and CDISC Controlled Terminology Management, and maintain all controlled and tracking documentation
    Provide technical, process, and project management leadership for assigned projects and the group in general
    Overall maintenance and coordination of CDISC standards efforts, ensuring maximum reuse of applied standards, involvement in ongoing process improvement efforts, and working with teams to provide technical and process guidance
    Stay current with the evolution of all CDISC SDTM standards and may also be involved in creation and maintenance of process documentation
    There is the possibility that you could be integrated into a study team to lead the SDTM implementation work, with responsibility for managing the task assignments to SDTM Implementers and study programmers.
    The position can be home based or in one of our offices in Cambridge, MA; Waltham, MA; or Chesterbrook, PA.

    Qualifications and Experience
    You will have a BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject, and a minimum of five years of relevant career statistical programming experience in a clinical development environment; six or more years highly desirable. Additionally, we require:
    Excellent SAS data manipulation skills
    Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
    Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
    Excellent oral and written English communication skills
    Ability to provide quality output and deliverables, in adherence with challenging timelines
    Willingness and ability to learn and follow standard processes and procedures
    Ability to develop SAS Macros (specification/coding/testing) in accordance with standard practice
    Ability to apply source code control procedures for custom SAS Macro Development
    Ability to lead and manage a team of SDTM Implementers in the successful and timely completion of all related SDTM activities for a study end to end
    Project management experience – prioritizing, resourcing, following timeline, issue tracking
    Strong SQL and SAS programming skills with respect to data transformation
    Detailed knowledge of CDISC SDTM standards and the principles on which it is founded
    An understanding of where the process of producing SDTM datasets fits within the overall statistical programming workflow
    Ability to code to conventions provided by Company/CDISC
    Ability to identify data issues that affect programming decisions or the integrity of results
    Hands-on experience on CRF annotation with SDTM mapping
    Experience managing SDTM controlled terminology
    Ability to quickly develop a detailed understanding of study protocols, annotated CRFs, controlled terminology, and raw datasets
    Prior leadership or management position
    Compensation & Benefits
    We offer a competitive salary-based package, bonus, comprehensive medical and dental benefits, plus a contributing 401K plan.

    Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

  14. Study Lead Programmer

    We are seeking a Study Lead Programmer for a recently expanded five year FSP contract with a well-respected, leading biotechnology firm. This high visibility technical role is responsible for directly managing a team of programmers, as well as providing appropriate guidance to other programmers. You will be tasked with ensuring that all timelines and quality standards are met and that all tasks (e.g. all programming related activities of a study) assigned to your team are aligned with the respective programmers’ abilities. Significant hands-on statistical programming is a key expectation for the role.

    Additional responsibilities include:
    Participate in establishing the programming scope for a deliverable with study statistician and study team
    Participate in establishing detailed timelines that will ensure timely deliverable
    Write protocol specific programming specifications
    Review and propose data specification for assigned protocols for SDTM and ADaM data
    Manage individual programmer work assignments to assure timely, high quality deliverables
    Review and critique QC documentation
    Provide technical leadership and guidance for study programming team
    Coordinate and monitor data issue reporting and resolution
    Coordinate with other leads to provide consistent deliverables across the assigned projects
    Serve as primary interface to study team and Amgen CDISC Consultancy and Implementation (CCI) group, if necessary
    Manage technical aspects of project (e.g., create/manage computing environment, lookup tables)
    Manage project tracking tools and provide periodic status reports to Company team
    Provide mentoring for all newly added FSP programmers
    The position can be home based or in one of our offices in Cambridge, MA; Waltham, MA; or Chesterbrook,PA.

    Qualifications and Experience
    You will have a BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subjectject, and a minimum of 5 years of relevant career statistical programming experience in a clinical development environment; six or more years strongly preferred. Additionally, we require:
    Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
    Ability to work effectively on multiple tasks or projects
    Willingness and ability to provide guidance to team members on technical and process questions
    Thorough understanding of clinical trial processes, from data collection to analysis reporting
    Proven record of superior statistical programming and problem solving skills within clinical development environment
    In-depth knowledge on latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards along with strong ability to implement all aspects of CDISC
    Prior experience and ability to lead and manage programmers in the successful and timely completion of all programming related activities for a study end to end
    Excellent oral and written English communication skills
    Compensation & Benefits
    We offer a competitive salary-based package, bonus, comprehensive medical and dental benefits, plus a contributing 401K plan.

    Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

  15. SAS Platform Administrator – Cleared (req# 15006273)

    Northrop Grumman Information Systems sector is seeking a SAS Platform Administrator 3 to join our team of qualified, diverse individuals. This position will be located in Vienna, VA.

    Put your years of experience into a future of excellence…the complexity, scale, and strategic importance of our customer’s environment necessitate an experienced administrator to ensure the successful implementation and
    continuing optimal operation. The job would be expanded to roles of technical/user support on our FinCEN application support team.

    Oversight of SAS Platform Administration
    Development and enhancement of the SAS Metadata layer and other administration objects required to successfully support the platform. Establishment of processes needed to grant system access, and control security appropriately. Plan and perform upgrades and patches. Participate in Disaster Recovery planning and exercises to ensure business continuity. Assess capacity versus demand, and forecast future needs for Expansion/scale-up. Assist with integration of SAS Platform with other technologies.

    Miscellaneous Platform Support
    • Development activities as related to support of server applications, table updates, etc. Oversee all outputs and access related to the Enterprise Data Warehouse (EDW), SAS environment, and other user web interface.
    • Oversee and audit approvals and the escalation of any non-compliance or inappropriate access requests. Facilitate Production Support team by directing the requests to the appropriate team members.

    Duties and Responsibilities:
    SAS Platform Support
    • Support SAS platform- start/stop server, trouble-shooting server issues
    • Create user accounts
    • Help SAS users tune query performance
    • SAS SME for functional support
    • Support and trouble-shoot custom-developed query audit logging system to monitor user queries
    Alert Generation Process
    • Support Prototype EG Alert System- deploy new rules, trouble-shoot issues
    • Support the new SAS Enterprise Rule Engine Design and Development utilizing SAS Financial Crimes Monitor (FCM) and SAS Social Networking Analysis (SNA) software.

    Basic Qualifications:
    • Bachelor Degree or an additional 4 years of equivalent technical experience will be considered in lieu of degree
    • A minimum of 5 years’ experience in a system administration role doing:
    Configuration of SAS servers to run within a Linux environment
    Creation of new users and user groups and assignment of ACLs
    Application of HotFixes/patches, new licenses to environment, licensing upgrade and migration
    • Knowledge of SAS Management Console (SMC), Metadata server, web service set up like JBOSS/Apache for the midtier
    • Experience configuring SAS/ACCESS to various databases (Oracle, MS SQL Server, ODBC, etc )
    • Base SAS, Macros, Proc SQL for debugging. Enterprise Guide experience a plus
    • Strong experience in Linux and WIndows operating systems and remote server operations
    • Support of SAS user scheduling tools
    • Active (or recently active; within past two years) Secret clearance and US Citizenship required

    Preferred Qualifications:
    • Ability to communicate complex concepts to various audiences (technical, user, management).
    • Experience with Bash and PERL
    • Good teambuilding skills.
    • Understanding of Data Governance concepts and/or audit.
    • Prioritization and ability to manage multiple projects simultaneously.
    • Knowledge of project life cycles and change control disciplines.
    • Willingness to learn new technologies and areas of specialty

    Northrop Grumman Corporation is a leading global security company providing innovative systems, products, and solutions in unmanned systems, cybersecurity, C4ISR, and logistics and modernization to government and commercial customers worldwide.

    Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/
    AA statement, please visit http://www.northropgrumman.com/EEO. U.S. Citizenship is required for most positions.

    To be considered send resume with full contact information to Karen.Kamienski@ngc.com

  16. Sr. SAS Platform Administrator (req# 15006002)

    Northrop Grumman is seeking a Sr. SAS Administrator to join our CFTC SAS Platform Support team. The successful candidate will work on-site at the CFTC headquarters in Washington DC.

    This position will be responsible for all aspects of SAS application, server, user, and SAS EBI platform administration, including implementation, configuration, upgrade, maintenance, coordination, problem resolution, testing, usage and performance monitoring and the design / development of SAS system infrastructure.

    This position will provide subject matter expertise, as needed, for CFTC Infrastructure, SAS application developers, analysts, economists as they deploy virtual servers in CFTC private cloud and use the SAS platform for daily business operations, including integration with different Data Sources (SQL server database, GreenPlum, csv files, etc.) and advanced analytics / data visualization.

    Qualified applicants will provide technical and consulting support for SAS Enterprise Guide, JMP, and SAS web applications in both the development and production environments.

    Basic Qualifications:
    • Bachelor’s degree and a minimum of 10 years overall technical experience
    • Minimum of 5 years SAS system administration experience encompassing entire SAS EBI suite of tools with in-depth understanding of SAS metadata server, application server, web server, web application server, SPD server, stored process server, load-balancing server cluster
    • Minimum of 5 years hands on experience with SAS Management Console, SAS EG, JMP
    • Minimum of 2 years hands on experience with SAS web tools, SAS Stored Processes, Macro, Graph, Stat, OLAP Cube, Information map, SAS BI Dashboard

    Preferred Qualifications:
    • Solid understanding of predictive analytics, data quality and data management concepts
    • Ability to work effectively with all constituents including economists, investigators, business users, data analysts, etc. being able to obtain feedbacks from all SAS users
    • Ability to manage mid-to-large SAS development projects
    • Experience in project management is a plus
    • Understanding of configuration management, change management and release management concepts and how they relate to application development and administration
    • Experience integrating SAS with a SharePoint presentation layer using Web Parts or web services or web application (HTML, CSS, JavaScript) is desired
    • Experience in systems support, user support, customer support or training of enterprise class software and/or hardware
    • Detailed knowledge of security, performance, server design, cross-platform architecture, system backup, recovery and storage administration
    • Strong oral and written communication skills

    Northrop Grumman Corporation is a leading global security company providing innovative systems, products, and solutions in unmanned systems, cybersecurity, C4ISR, and logistics and modernization to government and commercial customers worldwide.

    Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/
    AA statement, please visit http://www.northropgrumman.com/EEO. U.S. Citizenship is required for most positions.

    To apply send resume with full contact information to Karen.kamienski@ngc.com

  17. Jr. SAS Developer 2 – Cleared (req# 15002223)

    Northrop Grumman Information Systems sector is seeking a Jr. SAS Developer to join our team of qualified, diverse individuals. This position will be located in Vienna, VA.

    Put your years of experience into a future of excellence…The qualified applicant will become part of Northrop Grumman’s Team, supporting and enhancing various applications used to receive, process, store and analyze Bank Secrecy Act data sources for the Financial Crime Enforcement Network (FinCEN) government agency.

    In this role you will be supporting a project which includes onsite support of analysts using the SAS Fraud Framework components like Enterprise Guide, Enterprise Miner, Text Miner, SAS Alerts, along with ensuring the SAS environment is operational whenever the SAS database or database values are changed.

    Roles and Responsibilities:
    * Provide SAS user support to FinCEN staff
    * Provide users with refresher lab sessions on SAS Enterprise Guide
    * Capture various metrics of SAS helpdesk tickets
    * Provide SAS the capability to connect with additional
    * Support JIRA ticket release management

    Basic Qualifications:
    Bachelors degree and 2 years of related IT experience. An additional 4 years of experience may be substituted in lieu of degree
    Minimum 2 years of SAS experience in particular, experience with BASE, Enterprise Guide, Enterprise Miner, Text Miner, and SAS Alerts
    Must be able to demonstrate excellent verbal and written communication skills between the customer and all levels within the organization
    Position requires an active Secret Security Clearance. (US Citizenship required)

    Preferred Qualifications:
    Bachelors degree

    Northrop Grumman Corporation is a leading global security company providing innovative systems, products, and solutions in unmanned systems, cybersecurity, C4ISR, and logistics and modernization to government and commercial customers worldwide.

    Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/
    AA statement, please visit http://www.northropgrumman.com/EEO. U.S. Citizenship is required for most positions.

    To apply send resume with full contact information to Karen.kamienski@ngc.com

  18. BioStat For NAVY Marine Corps Public Health Center in Portsmouth VA.

    Relocation Assistance $3.500.00

    U.S. Citizenship required.

    Title Biostatistician/SAS Programmer

    Location Portsmouth, VA
    Salary Determined upon experience
    Hours 40 hours M-F Day
    Starting/Ending ASAP

    Description • Serve as a quantitative expert by formulating and developing innovative approaches to solve our clients’ most challenging business, technology and system integration problems.
    • The candidate will be involved in all aspects of data analysis and quality. He/she will analyze data collection plans and coordinate various data systems, implement data collection, processing, and analysis tactics, and provide consultation on design of data processing systems, which includes specifying needed output, required input and the methods of validation and quality control.
    • Investigate and identify data quality issues, and develop recommendation on how to resolve those issues to ensure data completeness, consistency and accuracy for the clients’ analytical products.
    • Apply knowledge in machine learning, data mining and natural language processing to create innovative solutions to our clients’ most challenging business and technology problems.
    • Collaborate closely with epidemiologists and clinical investigators to determine study design and formulate analysis plans. Consult with non-technical audiences to develop high quality client deliverables as well as effectively communicate the results to stakeholders. Design and implement validation tests for analytical products created by research staff. Provide SAS programming and troubleshooting support when needed.
    • Create and maintain documentation for generated work products

    Required
    Qualifications Basic
    • B.S. in Computer Science, Applied Mathematics, Statistics, Operations Research, Economics or similar quantitative field.
    • 3+ years of experience using SAS, including base SAS, to conduct advanced statistical analyses.
    • Ability to write highly efficient SAS programs using advanced procedures, macros and arrays.
    • Experience with manipulating large complex databases to track and evaluate patterns related to healthcare or other business processes.
    • Experience with managing projects in a consulting environment, including identifying requirements, determining priorities, tracking and resolving issues.
    • Ability to work effectively in a multidisciplinary team setting.
    • Strong oral and written communication skills.
    • Ability to obtain a secret security clearance. (U.S. Citizenship required)

    Preferred
    • Experience in developing applications using machine learning and/or Natural Language Processing (NLP) tools.
    • M.S. in Computer Science, Applied Mathematics, Statistics, Operations Research, Economics or other similar quantitative field.
    • 7+ years of experience using SAS, including base SAS, to conduct advanced statistical analyses.
    • Experience with advanced expertise in a broad range of statistical techniques, including experimental design, hypothesis testing, and multivariate regression.
    • Experience with database tools and SQL for data manipulation, aggregation, and validation.
    • Experience using UNIX based systems.
    • Proficiency in a scripting language, such as Python or R.
    • Experience in using Business Intelligence (BI) and visualization tools, such as Tableau.
    • Knowledge about the health care industry/health market.
    • Base SAS Certification.


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