Marketing Analytics Manager with SAS (Cheshire, UK)

Head New Management with SAS skills

An exciting opportunity has arisen to join a nationally accredited Financial Services provider in the North West of England. Your role will involve co-ordinating and managing a team of analysts in the application of analysis to drive commercial and marketing activity across all of this company products and channels. The team are responsible for targeting, profiling, in depth campaign analysis and generally adding value through the application of analysis, and this is a good opportunity to kick employ your innovative flair as the company looks to break the boundaries and explore alternative channels of contact with consumers.

It is essential that you have proven experience in behavioural analysis stored on large databases accessed via SAS or SQL. The opportunity would suit a candidate in a siilar role or senior analysts looking for a position of increased responsibility and accountability. You should have a numeric based degree e.g. statistics or econometrics and upwards of 4 years direct experience in managing analytical resources. Should you be ambitious, confident and passionate about analysis, apply immediately for this role. Fantastic package; £40-£45k + impressive benefits!

You can also visit our website www.corporate-recruiter.co.uk to view other various Statistical roles.

Location: Cheshire Salary: Negotiable - £40 - £45k

To apply or for more information: Please reply to this e-mail, or send mail to: sarah@coporate-recruiter.co.uk, or telephone 0207 861 9987. Please quote ref: AS/ 9913 /FG in the subject line

URL: www.datashaping.com/jobs16814f.shtml

Please mention datashaping.com when applying. Thank you.

SAS developer (Harrisburg, PA)

We have an urgent requirement for one of our client in Harrisburg, PA area for a SAS Developer. The successful candidate will function as level 2 technical support for a web-based self service reporting application. The candidate will research technical issues and develop, test and implement fixes or changes as needed.

Requirements:

• Ability to absorb and adhere to architectural guidelines established by corporate and departmental policy
• Ability to work with individuals of different backgrounds, abilities and temperaments in a team-based development environment
• Ability to work interdependently: sometimes self-directed, sometimes in detailed collaboration with others
• Ability to translate solution design into technical specification and modular program code
• Experience developing Reporting/Business Intelligence applications
• Strong Skills in SAS report programming using SAS version 9.1.3, particularly PROC SQL, PROC REPORT, SAS/GRAPH and ODS.
• Must have sound knowledge and skills in use of SAS macro,
• SAS/Connect, SAS/Access and the UNIX environment. UNIX scripting skills a plus.
• Must be familiar with modular programming and the ability to investigate and resolve issues, with sound code debugging skills.
• Must have strong written and verbal communication skills
• Experience using SQL, on RDBMS systems such as Oracle or Teradata and experience in the Healthcare Payor Industry, especially client reporting is a plus.

Deepak A N Technical Recruiter Comtec Information Systems http://www.comtecinfo.com 703-496-4813

URL: www.datashaping.com/jobs16838f.shtml. Please mention datashaping.com when applying. Thank you.

SAS Programmer, Clinical Programming (Italy)

SAS Programmer, Clinical Programming within Data Management - Permanent Role - Based in Italy

SAS Programmer - Data Management Specialist Technical Data Manager - SAS Specialist Based in Italy Excellent Salary + Benefits + Career Prospects

Job Summary:

An international company expanding its Clinical Data Management Team and looking for a Clinical SAS Programmer. Reporting directly to the Head of Data Management and Statistics, the Clinical SAS Programmer will be responsible for programming within data management / technical data management tasks.

Accountabilities/Responsibilities:

• Design case report form (CRF and eCRF)
• Design and / or review database structure
• Write edit checks from the Data Cleaning Plan (DCP) specifications
• Generate and manage Queries / eQueries
• Create derived-analysis datasets
• Execute, if required, analyses specified in the Statistical Analysis Plan (SAP) under the guidance of the project statistician
• Act as programmer to produce tables, listings, and figures for the clinical study report (CSR)
• Act as programmer to validate SAS programs that produce derived-analysis datasets and data analyses

Essential Skills & Capabilities:

Successful candidates will have the following skills/experience:

• 2+ years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries
• Good working knowledge of Base SAS, SAS Macro, SAS Language and SAS Stats software
• Good knowledge of English language, written and spoken

If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

We also have a broad variety of other Biometric specific vacancies available in the UK and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions, Regulatory Affairs, Clinical Research, QA, Compliance & Validation.

For a confidential consultation, email your CV to: james.carrera [at] 1st-pharmapeople.com

URL: www.datashaping.com/jobs16816e.shtml Please mention datashaping.com when applying. Thank you.

SAS Senior Director of Business Analysis (Raleigh, NC)

We have a Client based in Raleigh , East Coast USA seeking a Director of Business Analysis , the Candidate MUST have SAS and Knowledge of Pharma. The Sr. Manager/Associate Director, Business Analysis will lead, develop and coach a team of Business Analysts in basic and advanced analytics and sales reporting. In addition, the Sr. Manager/Associate Director, Business Analysis will perform advanced, business-driven analyses (return on investment (ROI), promotion response, sample optimization), manage all prescription data reports, interpret results of analyses for internal customers, maintain database of ad hoc data requests with disposition and maintain SOPs, WPs and compliance with PDRP. The Sr. Manager/Associate Director, Business Analysis will manage the relationship between client and vendors as required.

Responsibilities:

We seek a candidate with a Master's degree or higher in a quantitative field and at least 4 years experience in pharmaceutical business analytics. Must be an advanced user of SAS for statistical analysis in a pharmaceutical context. The ideal candidate will have experience with cluster analysis, multivariate regression, event history analysis, neutral networks, ordinal categorical regression and other statistical methodologies. The successful candidate will possess strong interpersonal, organizational and workload planning skills along with excellent verbal and written communication. Must have previous experience working with pharmaceutical sales data. Experience managing analytic professionals strongly desired.

Shula George Fforde USA 001 212 520 8303 shula [at] fforde-management.com

URL: www.datashaping.com/jobs16836e.shtml Please mention datashaping.com when applying. Thank you.

Statistical SAS Programming Opportunities - I3 (US)

Job Description i3 Statprobe provides a full range of data management and biostatistical services for the pharmaceutical and biotechnology industries. We not only pay relentless attention to the details, we also lend a broader perspective to a client's data management needs. We realize that strategy is just as important as process, and we provide a higher level of thinking for data management and biostatistics. As a UnitedHealth Group company, i3 Statprobe is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you can prepare for yours with us. It's a rare combination for success that only a career with i3 Statprobe can provide. We currently have openings for a number of experienced Statistical Programmers for all levels and in several i3 office locations.

Position Levels

- Statistical Programmer - Sr. Statistical Programmer - Principal Statistical Programmer

i3 Locations

- Ann Arbor, Michigan - Austin, Texas - Cary, North Carolina - Eden Prairie, Minnesota - Lexington, Kentucky - Lenexa, Kansas - San Diego, California - West Chester, Ohio - Westerville, Ohio

Statistical Programming

From the SAS Institute to the Smithsonian Institution, i3 Statprobe has been recognized repeatedly for its programming innovations. Our operations programmers are renowned in the industry for their skill and ingenuity in developing programs to support study reports and regulatory submissions. Our core strengths run the gamut from developing NDA-ready data listings, summary tables, and statistical figures to creating integrated safety databases and other regulatory support tasks.

Responsibilities

The Statistical Programmer is responsible for the development and maintenance of statistical analysis programs to support clients' drug development projects.

Minimum Qualifications

Higher level of positions available depending on experience

• BA or BS in computer science, statistics, mathematics, or information technology.
• At least two years of SAS programming experience within the pharmaceutical industry.
• Extensive knowledge of SAS
• Experience working on clinical trials highly desired.

For more information on i3, please visit our website: www.i3global.com You may apply directly through UnitedHealth Group's website:

http://www.unitedhealthgroup.com/careers/

Or contact: Aaron S. Litwin Sr. Recruiter Aaron.litwin [at] i3statprobe.com

URL: www.datashaping.com/jobs16831d.shtml Please mention datashaping.com when applying. Thank you.

SAS Consultant, contract (Richmond, VA)

Req. ID: 14966VA Position Title: SAS Consultant Contact Name: Roy Sreedhar (roy@vls-systems.com) Location: Richmond VA Duration: 6 months Required Skills: Unix scripting, SAS Macros,data set manipulation, statistical analysis

Job Description:

Hands-on design/development experience and independent working

• Proficiency in BASE SAS, SAS Macros, data set manipulation, statistical analysis
• Proficiency in UNIX scripting
• Good communication - written and verbal

Secondary skills

• GUI interface experience using VB or SAS AF
• Teradata SQL
• MVS mainframe familiarity, JCL knowledge.

Includes development and maintenance work in SAS (Typical functions include statistical analysis, graphic presentation, or data set manipulation). Must have Unix scripting, SAS Macros. Teradata experience is preferred.

URL: www.datashaping.com/jobs16812c.shtml Please mention datashaping.com when applying. Thank you.

Analytics Professional Certification

What does Data Shaping mean?

The term was created in 1999 to fill a gap between data mining and statistics. Data shaping is about employing advanced statistical techniques to problems usually handled by computer scientists (machine learning, knowledge discovery, artificial intelligence, web mining). A data shaper is a true software engineer or computer scientist, and a true statistician at the same time, capable of extracting actionable information from large data sets, in production mode, to optimize business.

What are the Requirements to be Certified?

Professionals with an approved resume are allowed to display our logo with the mention Data Shaping Certified on their resume. The repository of certified professionals, is accessible to employers. More than 1,500 people are DataShaping certified analytic professionals.

To be eligible, You need to have a graduate degree from a respected university, with recent analytical expertise either in biostatistics, statistics, quality control, econometrics, quantitative or computational finance, ETL, data warehousing, data analysis, CRM, artificial intelligence, data mining, knowledge discovery, pattern recognition, business intelligence, electrical engineering, mechanical engineering, computer science, physics, operations research, predictive modeling, forecasting, time series, statistical programming (SAS, Splus, SPSS), customer profiling and segmentation, QA, six sigma, survey analysis, web analytics, text mining, bioinformatics, actuarial science, web mining, mathematics, market research, decision science, marketing databases, competitive intelligence, risk management, fraud detection or similar expertise.

Active recruiters serving the analytical community are eligible as well. Recent graduates with an analytical major and good grades, from a respected University, are also eligible, even if they lack work experience. Certification categories include

• DataShaping Certified Engineer
• DataShaping Certified Analyst
• DataShaping Certified Statistician
• DataShaping Certified Scientist
• DataShaping Certified Expert
• DataShaping Certified Professional
• DataShaping Certified Recruiter

You are welcome to use the category that best fits your profile.

How do I get Certified?

The DataShaping Certified status is granted after approval by our team of experts, including world class statisticians and data miners. There is no associated cost. To apply, e-mail us at vincentg@datashaping.com with DataShaping Certification in the subject line. You need to provide

• A link to your bio, resume or profile for us to check your qualifications
• Or a copy of your resume
• Your real name

Your credentials will be evaluated by our team.

Selected members of our DataShaping group or LinkedIn network, as well as outstanding professionals and people with resume accepted and listed on DataShaping are pre-approved. To check your status, please use the status box below. Once certified, you will be notified.

Full details at www.datashaping.com/certified.shtml

Sr. Manager/Associate Director, Business Analysis (NC)

Job ID: 1146
Positions: 1
Location: North Carolina
Category: Information Technology/Sales Information

Overview:

The Sr. Manager/Associate Director, Business Analysis will lead, develop and coach a team of Business Analysts in basic and advanced analytics and sales reporting. In addition, the Sr. Manager/Associate Director, Business Analysis will perform advanced, business-driven analyses (return on investment (ROI), promotion response, sample optimization), manage all prescription data reports, interpret results of analyses for internal customers, maintain database of ad hoc data requests with disposition and maintain SOPs, WPs and compliance with PDRP. The Sr. Manager/Associate Director, Business Analysis will manage the relationship between Salix and Wolters Kluwer, Verispan and other vendors as required.

Responsibilities / Qualifications:

We seek a candidate with a Master's degree or higher in a quantitative field and at least 4 years experience in pharmaceutical business analytics. Must be an advanced user of SAS for statistical analysis in a pharmaceutical context. The ideal candidate will have experience with cluster analysis, multivariate regression, event history analysis, neutral networks, ordinal categorical regression and other statistical methodologies. The successful candidate will possess strong interpersonal, organizational and workload planning skills along with excellent verbal and written communication. Must have previous experience working with pharmaceutical sales data. Experience managing analytic professionals strongly desired.

Apply Online

URL: www.datashaping.com/jobs16784b.shtml Please mention datashaping.com when applying. Thank you.

Senior Statistical SAS Programmer, Contract (UK)

CONTRACT: Senior Statistical SAS Programmer Statistical Reporting within Health Outcomes. 6 months rolling contract

Job Summary:

For this major pharmaceutical client you will work with Health Outcomes specialists (Patient Reported Outcomes Specialist, Epidemiologist, Health Economist) and programmers based also in other sites. Primarily providing programming support to Healthcare Outcomes and the Pharmaco-Epidemiology team. Accountabilities/Responsibilities:

• Provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase I - III clinical trials, ISS & ISE, primarily using SAS.
• Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE), electronic submissions and Exploratory Health Outcomes Research Reports.
• This position will require a significant training investment for the use of client technology in relation to SAS macros, creation of analysis data sets and dataset structures. Need for ensuring standardization of programs where applicable.
• Apply knowledge of clinical data, the design and phases of clinical trials, statistics, relevant regulations and the pharmaceutical industry to the implementation of tasks.
• Handle complex statistical programming issues independently and be familiar with study programming issues. Bring ideas for new projects and take the initiative to solve issues.

Essential Skills & Capabilities:

• At least 4 years Statistical SAS programming experience with prior experience in pharmaceutical related field is required (experience with large databases is an asset).
• Working knowledge of clinical legislation (FDA, EMEA, ...), Good Clinical Practice (GCP) and Clinical Data Interchange Standards Consortium (CDISC) is a plus.
• SAS expert
• Statistical knowledge including basic statistics (descriptive statistics, inferential parametric and non parametric analyses) and advanced statistical techniques (multivariate analysis, ...).
• Fluent in English
• Ability to understand business problems rapidly and to reformulate them in terms of appropriate statistical analyses to be performed.
• Ability to evaluate processes and situations in an orderly and rational manner asking questions and identifying missing information.
• Accurately and efficiently work towards quality results

An excellent opportunity awaits for this renewable contract. Interview times booked and full job specification to review... If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

We also have a broad variety of other Biometric specific vacancies available in the UK and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions, Regulatory Affairs, Clinical Research, QA, Compliance & Validation.

For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera [at] 1st-pharmapeople.com

URL: www.datashaping.com/jobs16763e.shtml
Please mention datashaping.com when applying. Thank you.

Senior Statistical Programmer (NJ)

Our client is a contract research organization that provides statistical, data management, clinical trial monitoring and medical writing services to pharmaceutical and biotechnology companies, serving some of the best-known global organizations and working with many of the most advanced drugs in development. They require a Senior Statistical Programmer at their site in New Jersey who will be expected to perform a leadership role in statistical programming and reporting areas.

JOB ROLE: The Senior Statistical Programmer is primarily accountable for: statistical programming, validation and quality control of the statistical analysis datasets and output tables/listings/graphs; statistical programming and validation of database logical checks and study specific monitoring reports.

FUNCTIONAL RESPONSIBILITIES include:

• Designing statistical analysis dataset modules and creating complete, validated, efficient analysis datasets following common standards, conventions, and statistical instructions.
• Developing SAS programming codes and generating complete, accurate and validated statistical output reports of clinical trial data in well-defined formats.
• Developing and testing SAS codes for clinical trial database logical checks.
• Documenting data and programming information in accordance to corporate SOP and guidelines.
• Archiving clinical trial data (raw data and analysis datasets), and programming information in accordance to corporate SOPs and guidelines.
• Developing and providing expertise in other programming and system administration areas such as Unix, DataFax, Oracle and web according to business needs.
• Providing technical guidance and support to less experienced Statistical Programmers.

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:

• Bachelor’s degree in Computer Science, Mathematics or Statistics
• At least 6 years experience in clinical trial statistical programming.
• OR associate degrees with a minimum of eight years experience and demonstrated ability and sustained performance.
• Experience from within the Pharmaceutical / Clinical Research industry.
• Having the functional and technical knowledge and skills to do the job at a high level of accomplishment.

PERSONAL SKILLS & ATTRIBUTES:

• Action Oriented.
• Composure.
• Creativity.
• Customer Focus.
• Perseverance.
• Planning Accurately.
• Priority Setting.
• Problem Solving.
• Technical Learning.
• Time Management.

BENEFITS OF THE ROLE: A fast paced and rapidly expanding company that offers new challenges, interesting work and great career development opportunities that will enable you to progress and attain your goals. Their working environment is safe and pleasant and they provide a wellness program for all their employees. They are offering a competitive, flexible salary for this role plus benefits.

For applications or further information please email your CV to: shula [at] fforde-management.com, or telephone our specialist consultant, Shula George, on +1 212 520 8303 who will be pleased to advise you on your personal career needs. Alternatively you may write to us at 2nd Floor, 825 Third Avenue, New York, NY 10022 or Fax: 212-520-8501

Fforde is a uniquely specialized recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors. We pride ourselves on a glowing reputation within the industry and a high-quality personalized service dedicated to intelligent delivery. Explore our website and see all our job opportunities. www.fforde-management.com

KEY WORDS: Senior Statistical Programmer, Statistical Programming, SAS Programming, Statistical Reporting, Validation, Quality Control, QC, Statistical Analysis Datasets, Output tables, Listings, Graphs, Validation, Database Logical Checks, Study Monitoring Reports, Unix, DataFax, Oracle, Computer Science, Mathematics, Statistics, Clinical Trials, Drug Development, CRO

URL: www.datashaping.com/jobs16758e.shtml
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SAS Developer, Contract (Bridgeport, CT)

Req. ID: 14728CT Position Title: SAS DEVELOPER
Contact Name: Scott Narendra (scott@vls-systems.com)
Location: Bridgeport CT
Duration: 6-12+ Months
Required Skills: SAS, Data Step, financial, SAS Macros
Job Description: SAS Consultant Qualifications

Base SAS (Windows NT)

• Candidate must be able to follow program specifications to write, test, debug, document, and implement complex SAS programs to extract data from a variety of data sources, transform the data, and load the data to specified destinations.
• Ability to create SAS Data Sets from raw data extracted from various data sources and file formats, for example simple ASCII flat files; EBCDIC flat files; flat files with multiple layouts, (Header, Detail, and Trailer records); Excel spreadsheets; RDBMS tables; and SAS data sets.
• Ability to write output SAS data sets and flat files.
• Strong Experience with the Data Step.
• Strong Experience with SAS Sort and Merge functionality.
• In depth knowledge of the SAS Program Data Vector (PDV).
• Familiar with SAS arrays and PROC Tabulate.
• Excellent Knowledge of procedures like PROC SUMMARY, PROC TABULATE, PROC REPORT, PROC COMPARE, etc.
• Ability to use a variety of SAS formats and to convert from one data type to another.
• Strong knowledge of SAS functions.
• Ability to remove records with duplicate keys.
• Run SAS programs in batch mode.
• Experience with SAS 9.1 is a plus.

SAS MACRO

• Ability to write flexible and reusable code using SAS Macros.
• Experience in Assigning Values to SAS MACRO variables and evaluating SAS MACRO variables.
• Familiar with the differences between Data and Marco Variables.
• Complete understanding of Automatic, Global, and Local MACRO variables scope.
• Ability to use positional parameters and to assign default values to the parameters to MACROS.

PROC SQL

• Ability to Connect using SAS interface to ODBC.
• Strong Experience with Queries; Inner and Outer Joins; Merging; updating large data sets; and removing duplicates.
• Ability to create tables and views.
• Understanding of Indexes.

SQL

• Knowledge and Strong Experience with databases like Oracle, Sybase, and M! S SQL Se rver.
• Proficient in implementing Data Warehousing Solutions.
• Ability to perform Selects, Updates, Inserts, Deletes on database tables.
• Knowledge of Sybase and MS SQL Server BCP is a plus.

General Qualifications.

• Strong Leadership qualities and a self starter.
• Excellent Oral and Written Communication skills
• Strong Technical, Analytical, and Organizational Skills.
• Ability to work independently on projects.
• Team Player with excellent inter-personal skills.
• Ability to work under pressure and meet challenging deadlines.
• Ability to interact with End Users and Business Analysis
• Experienced with all phases of the Software Development Life Cycle (SDLC).
• Ability to Estimate Work Effort.
• Banking Experience is a plus.
• Familiarity with DOS commands is a plus.

URL: www.datashaping.com/jobs16754d.shtml
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SAS Programmer, Contract (Switzerland)

Our client, a global giant in the pharmaceutical world, is known as a leading name in the discovery, development and marketing of innovative pharmaceutical products which cure diseases, ease suffering and enhance the quality of life. They are seeking a SAS Programmer in a contract position for 6 months in Switzerland.

PRINCIPAL RESPONSIBILITIES include:

• Programming according to specifications, analysis datasets, listings, tables and figures for phase 3 studies including DMCs and providing support for SCS/SCE.
• Supporting quality control and quality audit of deliverables.
• Developing and complying with project/study programming standards and specifications following internal guidelines.
• Providing input into study protocol, CFR and data structure.
• Providing input as required at all meetings, discussions and activities covering aspects of statistical reporting on trial level activities.
• Supporting senior members of statistical reporting and programme/trial statisticians in maintaining efficient interfaces with internal and external customers

TECHNICAL SKILLS, KNOWLEDGE & EXPERIENCE:

• Experience using SAS in the analysis and the reporting of pharmaceutical data
• Working knowledge of database design/structures
• Expertise with SAS (including SAS macro language)

PERSONAL SKILLS & ATTRIBUTES:

• Good team player.
• Good organizational skills.
• Continuous improvement mentality and attention to detail.
• Fluent English (oral and written).

BENEFITS OF THE ROLE: The Company has been honoured to receive a place in Financial Times Top 50 best workplaces for two consecutive years. Employees feel a strong sense of job satisfaction and the company’s belief is that their employees deserve to be rewarded for excellence. They provide excellent training and development programmes and generous remuneration.

For applications or further information please email your CV to: den [at] fforde-management.com, or telephone our specialist consultant, Den Lowpetch, on +44 (0)1273 222964 who will be pleased to advise you on your personal career needs. Alternatively you may write to us at Curtis House, 34 Third Avenue, Hove BN3 2PD or Fax: +44 (0)1273 325350.

Fforde is a uniquely specialised recruitment agency for the pharmaceutical, clinical research and biotechnology sectors. We pride ourselves on a glowing reputation within the industry and a high-quality personalised service dedicated to intelligent delivery. Explore our website and see all our job opportunities. www.fforde-management.com

KEY WORDS: SAS Programmer, SAS Programming, Clinical Trials, Clinical Studies, Phase 3, Study Protocol, Study Deliverables, CRF, Statistics, Statistical Reporting, Pharmaceutical Data, Database Design, Database Structures, SAS, SAS Macro

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URL: www.datashaping.com/jobs16759c.shtml
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SAS Marketing Analysts (Derby, UK)

With a detailed emphasis on Data Manipulation you will provide key analytical value to this exciting Marketing department. Joining a team of experienced data analysts you will be key in providing in-depth analytical reports using statistical software SAS in a SQL environment. Driving this unique business area forward you will contribute to campaign management projects and competitor analysis. Solid commercial acumen is essential, as is the need to work effectively under pressure. Academically you will need at least a 2; 1 degree in a numerical discipline (Ideally Maths, STATS or Operational Research); and a minimum of 3 years commercial experience. If you meet the above criteria and a position with a major Blue chip sounds appealing please e-mail your CV ASAP.

E-mail resume to: n.duncombe [at] progressive.co.uk

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URL: www.datashaping.com/jobs16760a.shtml
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SAS Risk Analysts (Birmingham, UK)

Senior Operational Risk Analyst role with training on more complex SAS software and bigger Risk datasets, including Business Continuity.

These roles will see you taking responsibility for bigger and more complex analysis in Risk and Credit Risk, and also mentoring and guiding more junior analysts.

For these roles it is best to have an excellent track record in Credit Risk analysis and also good working knowledge of SAS, such as Base, Macro, Enterprise Miner etc. Experience in a Financial Services is an advantage.

These senior positions pay up to £35,000 plus an award winning benefits package. Click on the link below NOW to apply.

E-mail resume to: n.duncombe [at] progressive.co.uk

URL: www.datashaping.com/jobs16761b.shtml
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Sr SAS Analyst (Nottingham, UK)

An urgent requirement has arisen for a retail credit risk consultant to join a company that a household name in the financial industry. In your role will be responsible for with for working closely with key areas of the company, monitoring and managing portfolios to ensure that the business achieves its lending targets in an environment that balances risk with delivery of revue.

Technical skills for this role include:

• Strong SAS exposure
• Great levels of communication
• PC literate particular on MS Office products

This is an excellent opportunity to undertake a risk management role with a company that will actively look to more your career forward.

To apply for this role follow the link below or call Neil Hay @ Progressive on 0118 9159 123 for more details.

Key Skills: SAS EXCEL ANALYST STATISTIC STATISTICIAN SPSS

E-mail resume to: n.duncombe [at] progressive.co.uk

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URL: www.datashaping.com/jobs16762b.shtml
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