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The two positions below are in Hartford, CT.
Contact: scott@keyrequirements.com
Director, Research and Modeling - will relo, bonus, salary up to 115k - possibly higher.
SUMMARY:
Provides technical and quantitative analysis for predictive modeling group.
Brings business knowledge to help creatively solve business problems.
Assists in in-depth efforts applying and implementing predictive modeling results.
Directs analysts in research and predictive modeling projects.
Assists in statistical data mining and other actuarial research by applying advanced statistical concepts.
Uses computer technology, computer modeling, spreadsheet applications, software tools and programming languages.
Assists in designing reports to enhance analysis
Designs, writes and tests computer programs in model-building.
Participates in and may be responsible for projects requiring advanced statistical analyses, innovative research, mathematical calculations and technical skills.
May direct projects that have significant financial impact and may present to senior level management.
PRIMARY DUTIES:
Conduct research and predictive modeling.
Interpret data and identify correlations using both univariate and multivariate analysis.
Participate in discussions regarding underwriting strategy.
Communicate results and their implications to business centers.
Prepare responses to inquiries from business areas.
Oversee programming in SAS, VBA, Excel, Access or company software.
Participate in and/or is responsible for advanced projects.
Present findings to underwriting and actuarial management.
Provide assistance and supervision to less experienced staff.
WORK EXPERIENCE:
Generally 5 to 7 years of research, modeling or actuarial experience
Demonstrated ability in statistical modeling and data mining techniques (GLM, clustering, decision trees, etc)
Strong understanding of insurance related modeling and data
Strong project management skills
Knowledge of insurance products and operations
Basic understanding of accounting principles and solid understanding of financial reporting
Basic understanding of regulatory environment
CERTIFICATES/DEGREES:
College degree in statistics, mathematics, economics, finance, actuarial science or equivalent
Advanced degree in statistics (or related) or professional actuarial designation a plus
COMMUNICATION SKILLS:
Excellent communication skills
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Sr. Statistician - will relo, salary up to 115k, bonus
SUMMARY:
This position:
- Provides a high level of data mining, research and predictive modeling to achieve company objectives for profitability and growth.
- Apply advanced statistical concepts and data analysis methods in innovative research and modeling.
- Independently works on projects and may direct 1-2 analysts on project work.
- Develops new approaches to business problems using advanced statistical techniques.
- Researches new ways of using statistical methodologies.
- May assist with implementing model results into actuarial decisions and strategies.
- Responsible for projects requiring advanced statistical analyses, innovative research, mathematical calculations and technical skills.
- May direct projects that have significant financial impact and may present to senior level management.
- This position works under limited supervision.
PRIMARY DUTIES:
Conduct research and predictive modeling.
Interpret data and identify correlations using both univariate and multivariate analysis.
Offer recommendations to improve analyses.
Investigate and assist in data analysis.
Assist in summarizing results.
Perform advanced programming in SAS, Excel, Access or company software to perform modeling activities.
Engage in independent research.
Oversee limited projects involving predictive modeling staff.
Bring new ideas on statistical techniques and their application to the business.
WORK EXPERIENCE:
Either 7+ years of research and/or predictive modeling or 4+ years of modeling along with insurance experience.
Demonstrated ability in statistical modeling and data mining techniques (GLM, clustering, decision trees, etc).
Strong understanding of insurance related modeling and data a big plus
Strong project management skills.
Basic understanding of accounting principles and solid understanding of financial reporting.
CERTIFICATES/DEGREES:
Advanced degree in statistics, mathematics, operations research, economics, engineering or professional actuarial designation. PhD is a plus.
COMMUNICATION SKILLS:
Effective communication skills.
DEC 2009 BIOSTATISTICIAN AND SAS CLINICAL PROGRAMMER POSITIONS IN MASSACHUSETTS:
Principal Biostatistician-0901059 (Rockland, MA)
Description
* Function as a project biostatistician coordinating statistical aspects across clinical trials within a specific project in a therapeutic area
* With limited direction, provide statistical input for statistically complex protocol development
* With limited direction, write statistical analysis plans and perform statistical analyses for statistically complex clinical trials
* With limited direction, write statistical analysis plans and perform statistical analyses for safety and efficacy summaries for regulatory submissions
* Independently provide statistical input for statistically routine protocol development
* Independently write statistical analysis plans and perform statistical analyses for statistically routine clinical trials
* Participate in departmental standardization efforts
* Provide support towards statistical research
Key Tasks & Responsibilities
* Participate on clinical development teams
* Provide statistical input into clinical development plans
* With limited direction, participate in the development of statistical standards for clinical development programs
* Review statistical analysis plans written by other statisticians on the project
* Review statistical analysis results produced by other statisticians on the project
* Review statistical methods sections and the interpretation of results written by other statisticians on the project
* Provide statistical support for manuscripts and review manuscripts for accurate statistical interpretation
Functional Roles and Responsibilities:
* With limited direction, provide statistical input for protocol/CRF development (e.g., trial design; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough evaluation of results section; effective CRF specifications to collect data specified the protocol)
* With limited direction, write statistical analysis plans for clinical trials as well as for integrated safety and efficacy summaries. Analysis plans written include the most appropriate statistical methodology and data presentations.
* With limited direction, analyze clinical trials
* With limited direction, write accurate, logical, clear, concise, thorough and objective statistical methods sections for clinical trial reports
* Review and co-author clinical trial reports ensuring the accuracy of the statistical interpretation
* Understand and follow all Global Biostatistics WIs/SOP as well as any other relevant WIs/SOPs. Provide input into all newly developed departmental quality documents
* Provide input into general standardization efforts (e.g., CRFs, query checks, statistical methodology, standard statistical programs, data presentations)
* With direction, interact with regulatory agencies regarding statistical issues
* With direction, develop responses to regulatory agency requests that maintain perspective and are within the appropriate context
* Participate effectively on clinical trial teams
* With direction, provide solutions for complex issues presenting alternatives and identifying the best solution
* With limited direction, communicate routine and complex statistical concepts and results to non-statistical internal and external colleagues in a clear, concise, focused and articulate manner
* With limited direction, function as the statistical primary contact with CROs for studies that are outsourced, and ensure the accuracy and timeliness of the CROs analysis alerting management to any unforeseen circumstances
* Produce assigned work within the timelines provided ensuring deadlines are met
Education/Languages
* Ph.D. or MS in statistics, biostatistics or related discipline
* Fluent in English (French or German is a plus)
Professional Skills & Experience
* Several years experience in the Pharmaceutical/Biotechnology industry
* Working SAS knowledge and proficient in SAS/Stat
* Knowledge of ICH Statistical and Clinical Report Guidelines
* Familiarization with relevant therapeutic areas
Personal Skills & Competencies
* Ability to work in a matrix organization
* Ability to work with multi-disciplinary groups
* Strong communication, negotiation and issue resolution skills
* Balance concurrent tasks and responsibilities
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Senior Statistical Programmer-0901356 (Rockland, MA)
Description
* Independently program (or write validation programs for) and document tables/listings/graphs for clinical trials or portions of clinical trials requiring routine data manipulation and analysis.
* Routine data manipulation and analysis with limited direction.
* Program (or write validation programs for) and document tables/listings/graphs for clinical trials requiring complex data manipulation and analysis.
* Provide input into general standardization efforts and create (or validate) global macros that streamline repetitive operations.
* Mentor biostatisticians and statistical programmer/analysts with advance SAS programming techniques.
* Interface with SAS technical support to resolve software problems.
* Coordinate, validate and implement SAS upgrades and licenses.
* Independently provide input into CRF specifications to collect data specified in the protocol and query with SAS technical support to resolve software problems, coordinate, validate and implement SAS upgrades and licenses.
* Independently provide input into CRF specifications to collect data specified in the protocol and query check specifications and provide input into analysis plan specifications and data presentations for clinical trials requiring complex data manipulation and analysis.
* Independently program (or write validation programs for) patient randomizations.
* Independently create (or validate) non-standard complex derived datasets.
* Create project and study phase sub-directories ensuring that all project work resides in the correct project and study phase sub-directories.
* Validate study phase flags in oracle tables and download study phase records from oracle tables to create analysis datasets.
* Audit changes to the database between study phases.
* Understand and follow all statistical and statistical programming SOP’s as well as any other relevant SOP.
* Lead process improvement teams as required.
* Effectively communicate analysis specification and programming/data issues that arise prior to or during analysis in a timely manner.
Professional Skills & Experience
* MS, BS (or equivalent).
* 6 years pharmaceutical/biotech or other relevant experience.
* Fundamental knowledge of relevant statistical areas.
* Fundamental knowledge of relevant clinical areas.
* Advanced knowledge of SAS/Bas, SAS/STAT; knowledge of SAS/Connect, SAS/Macro, SQL.
* Excellent communication skills
* Ability to independently solve complex problems logically.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Wellesley, MA
Biostatistics
Description
Responsible for providing statistical and programming support to Medical Affairs projects. Will participate in the development of study protocols including participation in study design discussions and running scenarios and modeling to determine the best strategy for any Phase IV study. Reviews CRFs and data edits. Develops statistical analysis plans including analysis files and report/programming specifications. Performs statistical analyses including the production of tables, listings and figures, interpreting statistical results, and helps prepare study reports for presentations and publications. Responsible for managing project related analysis and programming execution.
Detailed Responsibilities:
Protocol Design. Participates in protocol development ensuring that the design meets the objectives and is optimal within the imposed constraints. Performs sample size estimates and/or power calculations to evaluate the costs of various design scenarios. Reviews CRFs and data edits. Proposes methods for statistical analysis and prepares statistical section of protocols.
Analysis. Prepares statistical analysis plans (including specifications for analysis files and report tables), and performs the analyses of the clinical data.
Computing. Understands and utilizes those aspects of computer science necessary for efficient data management and statistical analysis. Conducts complex statistical analysis utilizing SAS and other statistical software packages, as required. Creates, maintains, updates, and documents SAS programs for statistical analysis.
Presentation of results. Interprets statistical results and presents findings in an appropriate format. Helps prepare the statistical methods and results sections of clinical study reports ensuring that graphical and tabular summaries are clear and concise and that the objectives of the study are addressed. Presents statistical results to non-statisticians for clinical interpretation. Also assists with development of statistical sections of manuscripts and presentations.
Maintenance of records. Maintains project files ensuring adequate, clear documentation of data sources, management and analysis.
Consultation. Provides general consultation and training to appropriate Company personnel, usually on an informal, as-needed basis.
Professional Development. Maintains proficiency in statistics through training courses, participation in appropriate societies, review of professional literature, industry and academic contacts, etc.
Requirements
MS with 3 years or PhD with some experience working on clinical trials in the pharmaceutical industry and/or biotechnology industry.Thorough understanding of statistical principles with the ability to practice and implement them. Ability to provide solutions to a variety of technical problems of moderate scope and complexity.Proficiency and experience in SAS programming, and knowledge of SAS procedures and other statistical software.Excellent written and oral communication skills including grammatical/technical writing skills.Effective communicator: able to explain methodology and consequences of decisions in lay terms.Effective team player: willingness to go the extra distance to get results, meet deadlines, etc.Able to be flexible when priorities change. Able to deal with ambiguity.Some knowledge of medical/biological terminology and clinical practice in relevant therapeutic areas is preferred.Working knowledge in FDA guidelines relating to statistical analysis, study reports and statistical components of new drug applications is preferred
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Location Marlborough, MA
BIOSTATISTICIAN
This position is responsible for biostatistical activities in support of clinical trials including: generating data tables, patient data listings and reports using SAS; preparing statistical analysis plans; contributing to the statistical section of clinical trial protocols; reviewing analysis of clinical trial data.
Duties and Responsibilities:
Under direct supervision performs the following duties:
Generates statistical summary tables, patient data listings and reports using SAS.
Performs quality control check of SAS programs.
Handles basic SAS programming issues as well as all other study programming issues.
Assists with UAT of SAS dataset transfer files.
Works with the Biostatistics Manager and Clinical Sciences staff to develop scientifically sound clinical study designs and contributes to the statistical section of clinical research protocols.
Contributes to or prepares statistical analysis plans under the direction of the Biostatistics Manager.
Prepares template and performs programming for periodic progress reports for assigned clinical programs.
Compiles clinical data and relevant background material, and presents these results to the Biostatistics Manager for review.
Minimum Education & Experience:
Master's level degree in biostatistics, statistics, or public health; Bachelor's level degree will be considered.
At least 1 year of experience in SAS programming; preferably 1 year in medical device or pharmaceutical clinical trials.
Demonstrated computer expertise in SAS programming and word processing; experience using SQL and EDC highly desirable.
Familiarity with clinical trial design and analysis issues.
Working Conditions:
General office environment, minimal travel.Master's level degree in biostatistics, statistics, or public health; Bachelor's level degree will be considered.
At least 1 year of experience in SAS programming; preferably 1 year in medical device or pharmaceutical clinical trials.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Senior Biostatistician
Southborough, MA
Description
The Senior Biostatistician fills a critical role within the Biometrics Department analyzing and interpreting confidential data from a variety of sources. Under minimal supervision the Senior Biostatistican is capable of working on highly complex projects suggesting analyses, compiling reports, charts and tables and interpreting results based on established statistical methods, relying on prior experience and judgment. Timeliness, excellent communication and professionalism are essential as staff in this position directly interact with personnel from a variety of technical backgrounds.
ESSENTIAL DUTIES AND RESPONSIBILITIES INCLUDE THE FOLLOWING:
Participate in the design and review of:
- Clinical protocols and case report forms (CRFs) including preparation of Statistical Considerations sections, sample size calculations, interim looks and study design recommendations.
- The database, data collection guidelines, and computerized logic checks used to assist data management.
Create analysis plans detailing the objectives, statistical considerations, study populations, efficacy parameters, statistical methods and prototype tables, figures, and listings.
Manage:
- Generation and implementation of the quality review process in conjunction with data management, biometrics, and programming support.
- Implementation of analysis plans.
Provide guidance and training to Biometrics staff on statistical procedures, methods and concepts.
Write and review statistical reports; provide statistical expertise to the Medical -Writer for integrated clinical and statistical reports.
Design and manage generation of randomization schedules.
Provide statistical support, potentially serving as primary contact, to clients and internal project team members.
Provide input on statistical management for all projects and departmental operations.
Prepare and review FDA statistical responses.
Provide independent FDA representation.
Participate in the interviewing process for departmental candidates.
Participate in revising Biometrics policies, guidelines and operations.
May serve as back-up biostatistician on other projects.
Perform all other duties as assigned.
Requirements
Ph.D. in Biostatistics or related discipline and 3years of experience with at least 1 year in a CRO, or a Masters degree in Biostatistics or related discipline with a minimum of 4 years experience, at least 2 years in a CRO.
Preferred Qualifications:
Ph.D. in Biostatistics and 4+ years industry experience including 2 years in a CRO; experience as a mentor, team leader or manager.
ESSENTIAL KNOWLEDGE, SKILLS & LICENSES:
Must have advanced computer skills with expertise in SAS, StatXact and nQuery
Must have strong problem solving and creativity skills; proven leadership skills; good time management skills; the ability to prioritize, and multi-task.
Excellent organizational skills with ability to work in a high volume and strict deadline environment
Excellent interpersonal skills
Excellent verbal and written communications skills
Ability to work independently and as a team member
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Biostatistician
Cambridge, MA
Biostatistician
As a Biostatistician you will work within scientific affairs, and closely with data management, regulatory & other functional groups to provide strategic input into observational research on the natural history of disease and comparative safety and effectiveness, to propose methodologically and statistically
sound study design and data analysis plans to meet project objectives and regulatory requirements, and to conduct and supervise performance of analyses, evaluation and reporting. In this role, you will recommend and conduct biostatistical activities in support of the design and completion of observational
studies, design and conduct descriptive and inferential statistical analysis, develop sample size/power calculations, and stratification or randomization schema along with consult on data collections methods and quality control to ensure availability and validity of required output for analysis.
The ideal candidate will have a doctorate in biostatistics with a strong analytic track record and at least 5 years of biopharmaceutical experience. Candidates with an MS degree in biostatistics or statistics degrees and significant statistical and analytic experience may also be considered. Experience with general linear models, logistic regression, non-parametric and exact procedures, Bayesian analysis, and study size calculations along with having the ability to convey biostatistical principles is required. Also needed is a demonstrated ability to recommend plans for research design, strong working knowledge of relevant statistical methodology, experience in SAS and having the ability to work on multiple projects.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Senior Biostatistician
Massachusetts-cAMBRIDGE
The incumbent will:
-Have Ph.D. or Master’s with 5+ years in Statistics or Biostatistics
-Support internal clients through out MDx.
-Represent Biostatistics on project teams and serve as primary liaison to key internal clients with regard to resource needs and timelines.
-Interact with FDA or other regulatory agencies as needed in statistical aspects of study design, data analysis and statistical procedures; interpret the project implications of regulatory guidelines.
-Manage, mentor direct reports, and provide them opportunities for their self development
-Develop Biostatistics procedures and guidelines to comply with corporate quality polices
-Provide technical leadership and initiate methodological research to improve the methods current in use.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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BioStatistician /SAS Programmer
Location : Cambridge, MA
Seeking a highly-qualified biostatistician to provide support for the clinical development of antiviral products.
Responsibilities:
· Prepare SAS programs/macros for safety tables, listings and graphs, occasionally for efficacy tables.
· Prepare SAS programs/macros for validating data.
· Prepare SAS programs for generating analysis database and ISS/ISE databases.
· Assures quality by validating programs written by other programmers.
· Convert different formats of data files into SAS datasets.
· Prepare data analysis and graphical plots to support ad-hoc requests.
· Prepare required files for eCTD (Electronic Common Technical Document) for regulatory submissions.
· Participate in design, review and QC of database structure of clinical studies.
Requirements:
MS in Statistics, Biostatistics, or Mathematics with 3 years experience; or BS in Mathematics with 5 years experience Biotech or Pharmaceutical industry experience a must.
Experience with Phase 1 to 3 clinical trials and NDA filing. Proficient in SAS/BASE, SAS Macros, SAS/GRAPH, SAS ODS. Knowledgeable about SAS/STAT and eCTD
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Functional Area RD - Research/Development
Location MA - Norwood
Company Description
Client offers a broad portfolio of performance-driven diagnostic solutions that provide more effective and efficient ways to anticipate, diagnose, monitor and treat disease. Our products and services offer the right balance of science, technology and practicality across the healthcare continuum to provide medical professionals with the vital information they need to deliver better, more personalized healthcare to patients around the globe. Visit us at www.siemens.com/diagnostics.
Job Description
Conduct statistical analysis on data which includes descriptive statistics, analysis of variance, process capability. Write reports on the outcomes of the analysis of the collected test data and key finds.
Proficiency with SAS programming language. Strong oral and written communication skills. Previous statistic work experience in clinical research, manufacturing operations support and/or in-vitro diagnostics a plus.
BS/BA or advanced degree. Preferred disciplines: Statistics or Biostatistics
Desired years of experience: Up to 2 years applying statistical techniques in experimental design, clinical data analysis, clinical research or process control.
Preferred skills:
*Proficiency with stastical packages (Minitab, JMP)
*Experience developing queries or working with Oracle or SQL databases to mine data.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Massachusetts-Massachusetts
JOB DESCRIPTION: Senior Biostatistician
Master the knowledge of statistical theory and applications pertaining to design of experiments, general linear models and variance components. Knowledge and experience in analysis of high dimensional data, especially clustering and classification methods and predictive statistical models for genetics and genomics data. Capable of technically addressing and solving unique statistical problems. Knowledge of appropriate regulatory agency regulations and guidelines. Excellent oral and written communication skills. Strong interpersonal and leadership skills. Ability to provide clear, technically sound, well-communicated guidance to non-statisticians. Self-motivated; ability to work independently and complete work on a timely basis. Skilled SAS programming knowledge; other statistical package knowledge a plus. Pharmaceutical/Biotechnology industry experience in assay validation, quality control, process optimization and validation, design of experiments, and pharmacokinetics. Experience with coordinating/tracking of resources, others' workloads and multiple projects.
REQUIREMENTS - QUALIFICATIONS: Senior Biostatistician
Provide statistical consultation and analysis in support of research & development, clinical testing, and manufacturing of Novartis MDx products.
The incumbent will:
-Have Ph.D. or Master’s with 5+ years in Statistics or Biostatistics
-Support internal clients through out MDx.
-Represent Biostatistics on project teams and serve as primary liaison to key internal clients with regard to resource needs and timelines.
-Interact with FDA or other regulatory agencies as needed in statistical aspects of study design, data analysis and statistical procedures; interpret the project implications of regulatory guidelines.
-Manage, mentor direct reports, and provide them opportunities for their self development
-Develop Biostatistics procedures and guidelines to comply with corporate quality polices
-Provide technical leadership and initiate methodological research to improve the methods current in use.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
Novartis Diagnostics
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Cambridge, MA USA
MA-09-005
BioStatistician /SAS Programmer
Location: Cambridge, MA USA
Client is seeking a highly-qualified biostatistician to provide support for the development its antiviral products.
Responsibilities:
• Prepare SAS programs/macros for safety tables, listings and graphs, occasionally for efficacy tables.
• Prepare SAS programs/macros for validating data.
• Prepare SAS programs for generating analysis database and ISS/ISE databases.
• Assures quality by validating programs written by other programmers.
• Convert different formats of data files into SAS datasets.
• Prepare data analysis and graphical plots to support ad-hoc requests.
• Prepare required files for eCTD (Electronic Common Technical Document) for regulatory submissions.
• Participate in design, review and QC of database structure of clinical studies.
Requirements:
MS in Statistics, Biostatistics, or Mathematics with 3 years experience; or BS in Mathematics with 5 years experience Biotech or Pharmaceutical industry experience a must.
Experience with Phase 1 to 3 clinical trials and NDA filing. Proficient in SAS/BASE, SAS Macros, SAS/GRAPH, SAS ODS. Knowledgeable about SAS/STAT and eCTD
Interested candidates may apply on line at www.idenix.com or email a resume to MA-09-005.idenix@sonicrp.com
Don't forget to mention Nature jobs when applying.
Apply for BioStatistician /SAS Programmer
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Senior SAS Programmer - Southborough, MA
Specialty: Biostatistics
Description: Senior SAS Programmer
Our client is a leading international clinical research organization (CRO) with proven expertise in supporting global clinical trials for pharmaceutical, biotechnology and medical device companies. Our client's well-designed trials span the product development lifecycle from first-in-man through regulatory approval and post-marketing surveillance studies. Major therapeutic categories include: Oncology, Cardiology, and Medical Devices.
Job Description
Under minimal supervision the Sr. Statistical Programmer performs complex design and programming tasks. Requires interfacing with intra and inter-departmental project team members.
Write and debug statistical programming in SAS, and StatXact.
Ensure that project-specific derived dataset specifications and analysis programming specifications are complete and accurate.
Coordinate project-specific statistical programming resources including (1) defining timelines for batches of data displays in conjunction with the Biostatistician, (2) allocating appropriate programming responsibilities which take into consideration each programmers level of knowledge and experience as well as opportunities for growth, and (3) reviewing programming code.
Conceptualize, design, and implement programs and processes to standardize statistical programming across projects.
Assist in:
The definition of statistical programming conventions and procedures.
The evaluation of new software and enhancements to existing software.
Perform all other duties as assigned.
Job Requirements
Bachelors in Statistics or related discipline, with a minimum of 4 years relevant experience; or Masters in statistics with a minimum of 1 year relevant experience.
Preferred Qualifications:
Advanced coursework. Experience in a CRO. Experience as a team and/or project lead. Experience in UNIX.
Salary: $90,000 Annual.
CONTACT: SCOTT@MCKEARNEY.NET
WWW.KEYREQUIREMENTS.COM
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Sr. Scientist - Cambridge, MA & Irvine, CA
Department: Science
Applicants for Irvine, CA opportunities should submit resumes to irvinecstr@curiousconnections.com (please mention position of interest in subject field of the email)
Job Description:
Recent Ph.D. from a top tier school in statistics or applied statistics (such as econometrics or psychometrics or marketing research). Will work under leadership of domain architect to build best-of breed statistically robust platforms. Must demonstrate In-depth understanding of Bayesian methods and estimation with MCMC methods. Must demonstrate creative statistical thinking for problems and familiarity with techniques like factor and cluster analysis, modeling/estimation with unbalanced panel data, multidimensional scaling and latent variable modeling/estimation. Activities range from data management/exploration to recommender performance modeling/tuning to creative identification and estimation of preference-models and classification-schemes
Required Experience:
Recent Ph.D. from a top tier school in statistics or applied statistics (such as econometrics or psychometrics or marketing research). Must demonstrate In-depth understanding of Bayesian methods and estimation with MCMC methods. Must demonstrate creative statistical thinking for problems and familiarity with techniques like factor and cluster analysis, modeling/estimation with unbalanced panel data, multidimensional scaling and latent variable modeling/estimation.
For Cambridge Positions: marticstr@curiousconnections.com
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