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Senior Clinical Programming Specialist
Contract position is in Palo Alto, CA
-
Job Number: C10256
We work with contractors on a temporary W2 basis, or with Incorporated entities,
provided the nature of the work meets the qualifications that will allow the use
of an Independent contractor as defined by the IRS
Job Description:
Provide technical and statistical programming related expertise and advice
to the statistician and all Clinical Team members within assigned RB clinical
projects.
Manage and perform software development to support all regulatory, publication
and business events as required by the projects.
Participate actively as required as a technical resource to Clinical Teams
Work with the Project Statistician to establish study and project standards
in analysis, reporting and query software
Evaluate software requirements and alternative approaches, and plan software
development activities. Manage the processes of software development, validation
and execution to support all study reporting needs
Plan data validation and derivation programming and manage the execution and
validation of this programming
Provide technical advice to Clinical Programming Specialists and other assigned
or contracted staff as required.
Administer and comply with all relevant SOPs, Policies and Guidelines
Contribute where appropriate to the development of RB standards for the data
management and reporting of clinical pharmacology studies
Administer the security system for RB clinical staff access to Oracle Clinical
and data analysis and reporting repositories, as required
Perform as required the duties of the Clinical Programming Specialist
Provide effective statistical and database programming support for RB projects
and studies as assigned, including programming for study analysis and reporting of
clinical trials, performance of study randomization, creation and implementation of
validation and derivation procedures, and management of electronic data
Advice in protocol writing, database, quality specification and CRF design,
technical assistance in resolving study conduct and data management issues, and
analysis support for IND filing and reporting for RB projects and studies as assigned.
Effective implementation of software standards for assigned RB projects and studies.
Appropriate input to RB process and procedure development.
Maintenance of secure, and validated data storage and processing environment with
appropriate levels of access for all RB clinical staff.
Effective implementation of RB and relevant RGD standards
Identify data quality issues and communicate them to the appropriate Clinical
Team members
Candidate requirements:
Requires a BS/BA or MS/MA degree or equivalent in Computer Science, Statistics or other sciences
Requires approximately five years experience in statistical programming in the pharmaceutical industry.
Excellent programming skills in SAS and knowledge of the Oracle/Clinical database.
Excellent communications abilities, good interpersonal and project planning skills, and
knowledge of the drug development process.
Contract Length: 6 months with a contract-to-hire option
Contact Details
Heather Brown
Technical Recruiter
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
Email:
Web: www.thinknicity.com
Statistician in Northern New Jersey
must be a US citizen or green card holder.
Statistician
Ph.D. in Statistics, Biostatistics, Mathematics, or Masters and closely
related discipline, with 0-5 years experience. Knowledge/coursework in
mathematical statistics, linear statistical models, design of experiments,
regression, nonparametrics, Bayesian inference, stochastic processes and
applied probability, multivariate analysis, and categorical data analysis
required. Knowledge/coursework in statistical quality control, survey
sampling, nonlinear regression and empirical modeling, modern regression
methods, generalized linear models, optimization, and simulation highly
desirable. Coursework in physical, biological, or social sciences a plus.
Working knowledge of SAS or S-plus required. Knowledge of C++, Visual
Basic, or other programming languages desirable.
Contact:
Barry Rosen
Global Search Recruitment Systems, Inc.
973-781-1900 x 301
Email:
Web: www.gsearch.com
Boston Based SAS Opportunity
SCOPE OF RESPONSIBILITIES
Primary duty is to drive the direction of all statistical modeling work for client's organizations.
This includes the planning and creation of house file models to predict most responsive customers.
Manage relationship with outside firms to develop prospecting models of potential customers.
Proactively mine demographic, geographic and transactional data for hidden relationships using
advanced statistical techniques like Chaid and Logistic Regression.
Drive the use Design of Experiments to measure the effect of testing strategies in all marketing campaigns.
SPECIFIC RESPONSIBILITIES
- Proactively mine historical marketing campaigns to understand the impact of variable changes
on the overall effectiveness of all direct marketing spending.
- Translate marketing requests into new and innovative marketing programs by using descriptive
and predictive modeling techniques.
- Drive the direction of all uses of advanced statistical modeling of the Bose Customer Database
and outside prospect lists.
- Direct outside vendors to develop statistical models for segmentation and predictive purposes
to increase the size and profitability of Prospecting campaigns.
- Design and ensure statistically valid testing methodologies for all marketing campaigns through
the use of Design of Experiments (DOE). Advance the use of DOE techniques within Direct to Consumer Marketing.
- Act as the statistical expert for the Direct to Consumer Marketing Organizations within company.
REQUIREMENTS
Education: Bachelor's of Science, Statistics, Math, Econ, Master's Degree, Ph.D.
Experience: 7-10 years of related statistical experience in the Direct Marketing field.
Requires expert knowledge of statistical principles, methodologies and techniques.
Expert knowledge of relational databases and the use of statistical tools like SAS or SPSS.
For Consideration, contact:
Tom Hull, Partner
mangieri/solutions
1 Riverside Road, 2nd Floor
Sandy Hook, CT 06482
Voice Phone: (203) 270-4800 x 101
Fax: (203) 270-4815
Email:
Chicago Stat Programmer Opening
Founded in 1976, The Cambridge Group has developed a reputation as one of
the most respected recruiting firms specializing in clinical trials. Our
well-established client network, continually developed over the past 26
years, retain us to not only represent candidates with the right skill sets;
but to go beyond and represent only those professionals who excel and are
considered to stand out amongst their peers.
Current Need:
Title: Statistical Programmer-Chicago Metro Area
Terms: 6 months initial assignment, $35-50/hr
Client: Large Pharma Company
Start Date: 2-3 wks after offer (immediate need, new position)
Local Candidates will be considered first.
Pharmaceutical company in the Chicago area is seeking a statistical
programmer to support ongoing clinical trials. Most of the assignment
involves programming and validation, and utilizing SAS Base, Stat, Macro,
and Graph to produce tables, listings and graphs with some analysis.
Master's in Statistics or Biostatistics required, plus at least 1-3 yrs of
experience as a SAS Programmer in a pharmaceutical or CRO environment. We
offer competitive fees if we hire someone you refer us who we successfully
place into this assignment (up to $2,500 per person).
Confidential Contact:
Spiro Michas
800-295-0332 or 203-226-4243 (x261)
Email:
To view current job listings visit our website at:
http://www.cambridgegroup.com/pharmaceuticals/search_pharmaceuticals.shtml
MARKETING ANALYST MERIDEN, CT
MARKETING
SHIFT YOUR CAREER INTO HIGH GEAR
Since we've arrived on the auto insurance scene, we've been determined to shake things up a bit.
Our solid reputation for top-notch service along with our competitive rates are helping us quickly
gain recognition and have created the need for a professional:
MARKETING ANALYST MERIDEN, CT You will assist with the construction of marketing measurements and
models to track and analyze the results of direct marketing data, using these to create
recommendations for marketing strategies and program improvements that you will present to senior
management as well as external partners.
To qualify, you must have a BA or a BS in a quantitative discipline with at least 3 years'
experience working in a business analyst capacity, preferably within marketing. Experience with
SAS, SPSS, SQL, or Access is required.
We are an equal opportunity employer m/f/d/v offering a competitive salary and comprehensive
benefits. Please send your resume, with salary requirement, to:
HR Dept.-MA/H
Fax: (203) 634-7315
Email:
RESPONSE INSURANCE Careers with Response for Responsible People www.response.com
Published in the Hartford Courant on Sunday, 7/14/2002
Associate Actuary - Windsor, CT
Discipline: Life Insurance & Financial Services
Title: Associate Actuary
Location: Hartford, CT
Posted: 7/10/2002 9:30:00 AM
Email:
Job Duties:
As part of an actuarial consulting team for a life insurance company, diagnose actuarial
problems and develops and implements solutions to meet clients' needs; assists in the
product development process by preparing profit runs supporting the pricing of new client
products; sets up models of assets and liabilities done in the course of merger and
acquisition assignments, demutualizations and cash flow testing; reviews experience
information and develops assumptions based on that experience; provides technical
assistance on proprietary software.
Special Requirements:
Must have a Bachelor of Science in Actuarial Science or Mathematics and four (4) years
experience as an Actuarial Assistant. Must have designation of Associate of the Society
of Actuaries with ongoing pursuit of designation of Fellow of the Society of Actuaries.
Must have strong computer skills with knowledge of Excel, Visual Basic and Access.
SAS knowledge preferred. Must have strong initiative, solid analytical skills and strong
interpersoanl skills.
Equal Opportunity Employer
Hours: 37.5 hours/week
Salary: $60,000/yr to $90,000/year DOE
Contact:
Meredith A. Ratajczak
Consulting Actuary
Milliman USA
80 Lamberton Road
Windsor, CT 06095-2126
(860)587-2110
Email:
Web: www.milliman.com
Positions in North Atlanta Pharmaceutical
These positions are in the statistics department. I work in that department.
We are a small group in the US, 4 SAS Programmers and 5 Statisticians. Our
department is in a build up phase. Our statistics staff is composed of
entry, mid, and senior level people. Our program staff is composed of entry
and mid level people.
We are currently looking for self-motivated individuals to fill our Senior
SAS programmer positions and welcome the interest of all qualified persons.
Send me a reply if you would like more information about the position,
company, or Atlanta.
John Jones
Email:
Advertisement for Sr. SAS Programmer
This position will be responsible to support Biostatisticians working on
clinical trials, generating summary tables, graphs and patient data
listings. A BA/BS degree is required and a Master's degree in mathematics,
statistics, computer, or related field is highly preferred. The candidate
must also have excellent SAS skills (at least 2 areas SAS/BASE, SAS/STAT,
SAS/GRAPH), good written and oral communication skills, be familiar with
Windows environment and have at least 2-3 years of SAS programming
experience in the pharmaceutical industry.
Advertisement for Sr. SAS Programmer - Amadeus Project (Ph-Clinical) Support
This position will be responsible to support the Amadeus project in the US
as well as support Biostatisticians working on clinical trials, generating
summary tables, graphs and patient data listings. A BA/BS degree is
required and a Master's degree in mathematics, statistics, computer, or
related field is highly preferred. The candidate must also have SAS
(Warehouse Administrator, AF, IML, and at least 2 areas Base, Stat, Graph,
) skills, good written and oral communication skills, be familiar with
Windows environment and have at least 2-3 years of SAS programming
experience in the pharmaceutical industry. Knowledge of SAS/PH Dataware,
SAS/PH Clinical is an asset.
UCB Inc. is a Belgian company specializing in chemicals, pharmaceuticals and
packaging films. All three of our divisions are represented at our US
headquarters in Smyrna, Georgia. For more information about UCB, please
check out our company website at: www.ucb-group.com.
Job opening-Senior Research Data Manager- Augusta, GA
The Office of Biostatistics and Bioinformatics at the Medical College of
Georgia has a job opening for a Senior Research Data Manager who is proficient
with SAS and familiar with FDA regulations. MCG is located in Augusta, GA.
Application procedures can be found at:
http://www.mcg.edu/Jobs/index.html
The job description can be found at:
http://www.mcg.edu/Jobs/profess.htm
(See Senior Research Data Manager:
Office of Biostatistics, PLN(5749-R4049))
If you apply for this job through Human Resources (which is the proper
route), please send me a note so that we can be sure that your
application finds it way to us.
*************************************************************
Email:
Office of Biostatistics AE-3035 Phone: (706) 721-0813
Medical College of Georgia FAX: (706) 721-6294
Augusta, GA 30912-4900
*************************************************************
Senior / Principle SAS Programmer/Analyst - PERMANENT - Boston, MA
My client is looking for a Full-Time SAS Programmer/Analyst to be responsible for SAS
programming components of processing and analyzing clinical trials data and safety
summaries for regulatory submissions, integrating SAS datasets into Excel using Direct
Data Exchange, using SAS and Excel to analyze clinical trial data, statistical tables,
listings and graphs for clinical trial reports. You will be interacting with other
departments in the development and standardization of databases, reports, edit checks and documentation.
Skills required include 5+ years of SAS programming in a pharmaceutical/biotechnical industry,
expertise with SAS/BASE and SAS/STAT as well as experience with SAS/CONNECT, SAS/MACRO, SQL and
Excel are helpful. Expertise with Clinical Trial design and analysis issues as well.
Client is very eager to find the right applicant and is open to relocation if required. We may
also consider a temp to perm type scenario if needed. The client is not able to sponsor non
Green Card/US Citizens at this time. Sorry. Compensation is dependant upon ones skill set.
For IMMEDIATE Consideration, Contact:
Justin S. Tulman
Michael Anthony Associates, Inc.
W: 781-237-4950 x33
W: 800-337-4950 x33
Cell: 508-361-0072
Email:
Web: www.maainc.com
Clinical SAS Programmer/Analyst - Contract position - Palo Alto, CA
Job Number C10250
We work with contractors on a temporary W2 basis, or with Incorporated entities, provided the nature of the work
meets the qualifications that will allow the use of an Independent contractor as defined by the IRS
Job Description:
As data analyst you will be responsible for generating data listing, summary tables, figures and performing
statistical analysis for clinical reports using SAS and or S-Plus programming.
You will be developing and maintaining interactive applications to expedite reporting of results using
SAS/AF and SCL; writing reports and other documents requested.
Candidate requirements:
BS/MS in statistics, mathematics or computer science.
Six or more years experience with SAS Base, Graph, Stat, Macro, AF, IML, SQL.
Your SAS experience must be within a clinical/trial environment.
Clintrial software and Unix systems is a plus.
Must be able to work effectively in a team environment and independently, have good written and
verbal communication skills and good time and project management skills.
Coordinate with Information Systems on server requirements and database maintenance
Contract Length: 6 months
Contact Details
Heather Brown
Technical Recruiter
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
Email:
Web: www.thinknicity.com
Analytic Recruiting Inc.
12 East 41st Street, 9th Floor
New York, NY 10017
Phone: 212 545-8511
Fax: 212-545-8520
Website: www.analyticrecruiting.com
Marketing Modeler - IN
The primary responsibility of this Indiana financial services firm is to develop and maintain custom
marketing models using the SAS software tools. This position will work closely with marketing and
risk to implement effective predictive modeling solutions for customer acquisition, retention, up-sell,
response and reactivation initiatives. Modeler will build models for applications such as response
propensity, chum prediction, propensity to purchase, profitability and up-sell potential.
Requires:
Minimum BS/BA in Computer Science, Finance-Accounting, Economics, Stats or similar quantitative degree.
Minimum of 2 years recent experience in the development of marketing or risk models.
Competency in SAS
Experience with statistical methods, including hypothesis testing, (marketing), EDA, study design,
logistic/linear regression, factor reduction (CHAID, Principal Components, and Factor Analysis).
Exceptional written and oral communication skills.
Salary to $85k
Refer to Job#JV144-SConsig and email MS Word attached resume to
Jamie Voronkov
Email:
register online at www.AnalyticRecruiting.com
Project Manager, Marketing Science - Midwest
Medium-sized research supplier with specialization in conjoint and discrete choice modeling techniques.
Project Manager will have full responsibility for marketing science projects and will eventually present
to top clients. Candidates must be hands-on practitioners with solid training in quantitative research
techniques - including conjoint and discrete choice modeling - preferably using SAS.
Salary to $80K.
Refer to Job#MM128-SConsig and email MS Word attached resume to
Maura Mandrano
Email:
register online at www.AnalyticRecruiting.com
Credit Line Assignment Manager - NY
NY financial institution seeks Credit Manager to:
- Design/implement/manage Credit Line Assignment policies for all credit card products and acquisition
channels and newly booked accounts, measure performance on revenue, credit loss, RAM and customer satisfaction
metrics with test Vs. control methodology.
- Create statement of CL strategy for products & channels, communicate strategy to all acquisition partners
(Marketing & Credit Operations), measure performance against strategy, and adjust strategies to increase earnings.
- Coordinate CL assignment policy management with Marketing & Credit Operations to ensure consistent
implementation of line assignment policies and procedures for new and newly booked accounts.
- Manage and grow team.
Requires:
5+ years of Credit Card experience with Acquisitions Risk Management, Portfolio Risk Management or Behavior Scoring responsibilities and prior involvement in Credit Line Assignment for new accoun
Masters in Business, Economics, Finance or Statistics
Financial Management (P&L responsibility) experience in Credit Card or other related field with experience in Credit Acquisitions, Credit Policy and decisioning
Strong verbal and written communication and project management skills.
Strong analytical and IT skills with experience in data extraction and analysis tools (SAS, Knowledge Seeker, etc.)
Strong general management, staff development and leadership skills. Self-starter.
Salary $110-130k
Refer to Job#RR249-SConsig and email MS Word attached resume to
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
Project Manager - Data Management & Analysis - NYC
Major NYC insurance company seeks Project Manager for Customer Knowledge Management group. This role
requires hands on heavy-duty data management, analysis and processing to support development and
implementation of marketing programs.
Responsibilities:
Interface with IT and BTS officers for managing the data needs of Customer Knowledge and Corporate
Marketing both for long term as well as ad-hoc on project by project basis.
Work with IT in leveraging the tools for tracking, result analyses and reporting of marketing programs.
Work with IT to set up future process to manage customer data flow as needed from time to time for
campaign management, etc. and deploy and operationalize customer segmentation data for future programs and customer touch points.
Work with external vendors and manage retained consultants.
Facilitate tracking and analysis. Operationalize models and segmentation criteria for marketing programs
and ensure that appropriate selections are made, Control and Test groups are set up and data supplied to the
external list processing vendors as required per program specs.
Provide support to other members of the Customer Knowledge team in their data needs, prepare data for
analysis, data transformation and interpretation of data after understanding it from data dictionaries and
talking to IT personnel.
Requires:
BS (MS preferred) in Statistics, Mathematics, Economic or Computer Science
3-5 years experience in similar role within Database Marketing department or statistical modeling
Advanced knowledge of SAS and all procedures especially SAS Macros
5 years experience in heavy-duty data management and analysis using SAS and data management tools
2+ years of experience working within a financial or insurance environment
Ability to run queries, track, report and extract data on Business Objects and SQL or similar programs
Knowledge of SAS Connect, SAS Access, File transfer protocols e.g. FTP, WAMNET
Complete proficiency on UNIX or Mainframe and PC environments.
Salary 80-90k
Refer to Job#RR246-SConsig and email MS Word attached resume to
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
Credit Card Acquisitions Policy Manager - DE Bank
Develop credit policy for judgmental decisioning in Credit Card acquisitions. Work with Credit Operations
lending units to define operational decisioning requirements and procedures. Develop Customer Management
Strategies for Judgmentally booked accounts. Develop requirements for data archiving. Extract decisioning
data for MIS reporting, analysis and performance tracking. Develop Quality Controls and MIS requirements.
Develop comprehensive feedback streams to improve Analyst decisioning. Identify scoring tools and vendor
products that will improve financial performance. Develop segmentation and analytical targeting and
performance measure for predictable loss, profit forecasting and policy actions. Monitor program/channel
based P&L's to understand financial results and report policy and processing results to management.
Requires:
3+ years of Risk Management or Behavior Scoring experience.
Bachelors in Business or Statistics
Experience in Credit Acquisitions, Credit Policy and decisioning
Must be highly self motivated, goal oriented and able to manage multi-dimensional projects, across multi-site environments
Strong analytical skills with experience in data extraction and Analysis tools (SAS, Knowledge Seeker, etc.)
Excellent written and verbal communication skills with experience presenting to senior management on a regular basis.
Salary $80k
Refer to Job#RR245-SConsig and email MS Word attached resume to
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
Senior Analyst, Marketing/Business Analysis - NY
The Corporate office of a NY based entertainment company is currently seeking a Senior Analyst for their
Business Analysis Department.
Key responsibilities include:
Performing business and statistical analyses in a PC and mainframe environment
Creating, testing, monitoring and maintaining screening processes
Own databases and programs used to evaluate profitability
Conducting advertising performance analyses in coordination with Marketing
Perform other analyses as required
Requires:
Masters degree, with one of the degrees being analytical
Knowledge of SAS and structured computer language (Visual Basic, Fortran, C, etc.)
Good communication skills
Business understanding
Salary $50-70k
Refer to Job#244-SConsig and email MS Word attached resume to
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
SAS Datawarehousing/Statistician - Switzerland
We have Urgent Requirements for our client from Switzerland(1)SAS datawarehousing: For a pharmaceutical client in
Europe which requires 15 people with SAS Datawarehousing skills, 8 of whom should be developers, and 7 statisticians.
It is a Clinical study required for the pharma industry.
The SAS programmer needs to have 5 years of experience, the statistician needs to have 2 years of experience. Both
should have worked with a pharma company.
Ms. Sheetal Shah
Sr. Resource Executive
Heads2you (Right Head 2 Right Job)
Versova View, Suit No. 11/4 B1,Four Bungalow
Andheri West, Mumbai 400 053 (India)
Tel : 91.22.6350381 / 6351557
Email:
URL : www.heads2you.net
Biostatistics JOB: Philadelphia area, PA
Prosoft Software Inc., a SAS Alliance Partner and biostatistics consulting
firm, has an opening at its Philadelphia area office for a senior level
Clinical Biostatistician. Candidate will be responsible for managing a
group of statisticians, writing statistical analysis plans and statistical
sections of protocols, generating statistical tables and graphs, and writing
statistical sections of clinical study reports.
The ideal candidate will have a Ph.D. in Statistics or Biostatistics with at
least 7 years of clinical trials experience (or an M.S. with at least 9 years of
experience) with proficiency in SAS and experience with NDA submissions.
Must have eligibility to work in the U.S. and excellent oral and written
communication skills. Excellent salary and benefits. Casual, friendly work
environment.
Interested candidates should send their resumes to:
Dror Rom, Ph.D.
Prosoft Software Inc.
1275 Drummers Ln, Bldg #1, Ste. 200
Wayne, PA 19087-1571
voice: 610-293-1686
fax: 610-293-1690
Email:
Employment opportunity- SAS Programmers - Boston, MA
I have a client in Boston, Ma. looking for some SAS programmers, either
contract or permanent.
They are looking for someone with 3-5 years experience, preferable industry
related experience with pharmaceuticals, biotech, or clinical.
Peter Tetrault
Computer Express, Inc.
301 North Avenue, P.O. Box 308
Wakefield, Ma. 01880
phone 781-246-4477
Toll free outside of Ma. 888-246-4477
fax 781-246-1434
Email:
Web: www.computerexpress.com
SAS jobs - MD, DE, PA, NJ
Currently recruiting for a number of mid-senior level full-time permanent
clinical SAS programming openings in the Northeast (MD, DE, PA, NJ.)
Please email or call for details. Also have a number of Biostatistician
openings. All openings are will large pharma and offer full relo
packages. Salary ranges are in the $70-100k range + 10-15% bonus.
Tawfique Hamid
610-825-3850 x 3050
800-220-3850 x 3050
Email:
SAS Position Available in the Mid Altantic Region
I am searching for a person who has 3 to 5 years of SAS experience to work as a
SAS Analyst evaluating the effects of marketing campaigns for this company.
They will use the results of this information to build other marketing campaigns.
This is a permanent position, pays very well and has outstanding benefits.
For further information, please contact
Carol Aitken at:
Email:
call (610)388-0587
Job: Research Associate - Washington, DC
RESEARCH ASSOCIATE
The Education Statistics Services Institute of the American Institutes for Research, a
well-established not-for-profit social science research and development organization,
seeks a Research Associate to support its client, the National Center for Education
Statistics (NCES). The Research Associate will work on survey operations and quality
improvement for the two fiscal collections (local education agency and state) of the
Common Core of Data (CCD) Survey System. Duties include performing data quality checks;
reviewing CCD fiscal reports for understandability, accuracy, and adherence to standards;
monitoring the production of survey files and file documentation; assistance in follow-up
communications with state education agencies; maintaining data plans; and assistance in
planning and implementing activities to follow up on suggestions for CCD improvements.
Successful candidate must be proficient in SAS programming; experience manipulating large
data sets preferred. Master's degree or Bachelor's with a minimum of two years' related
experience required. Knowledge of Excel table preparation and file management required.
Excellent writing and communication skills, the ability to work within a team environment,
and attention to detail required. Experience and/or interest in education issues and/or
fiscal data a plus. AIR offers an excellent compensation package and benefits including
tuition reimbursement and transportation subsidy. Convenient location in downtown DC.
Please forward resume with cover letter, independently written and edited writing sample,
and availability to:
Human Resources - CCD
American Institutes for Research
Education Statistics Services Institute
1000 Thomas Jefferson Street, NW
Washington, DC 20007
Email:
Fax: 202-944-5454
Website: www.air.org
EOE
Email:
Base SAS Programmer - Charlotte, NC
A bank is looking for an experienced SAS, Unix developer for a 6 month contract to perm position.
The qualified candidate must have at least 3-5+ years of SAS (Base), Unix (Aix), prior experience
with moving data within a large data warehouse (Terradata experience a plus), prior experience
working with FTP & Flat Files, Ability to move data over cross platforms (Teradata/Bacardi),
prior experience with data manipulation & extraction.
Technical Environment: PC & Legacy systems, Unix (AIX), SAS v 8.0 (Base SAS), Oracle Database, Teradata, Banking
Type: Contract to perm....after six months they would like to extend offer
PS - Please keep in mind Signature has a referral bonus program$$$.
Brent A. Hamilton
Phone: (888) 522-1020, x3010
Fax: (704) 334-9694
Email:
Web: www.sigconsult.com
Manager, Clinical Programming requiring 8 years of SAS
programming,
and a BS or BA in Science, Math or CS
Foster City, CA
Job Number is F1482
Fulltime position
This position will not accommodate third party or agency representation
Job Description:
As Manager of Clinical Programming, you will coordinate
interactions with all functional specialists (Biostatistics, Clinical Data
Management, Clinical Research, etc.) and in assessing manpower needs and
based on priorities, assign Clinical Programmers work within or across
therapeutic areas.
You will actively participate in establishing and monitoring
of project timelines and develop, implement and maintain programming
standards and department standards
Candidate Requirements
Generally requires a BS or BA in Science, Mathematics, or Computer Science
Must possess at least 8 years of SAS programming within a clinical environment.
Ideally, you will have advanced knowledge of SAS report
writing and macros; superior communication skills and excellent
interpersonal and organizational skills.
Contact:
Sara Schmidt
Email:
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
www.thinknicity.com
Contact:
Heather Brown
Technical Recruiter
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
Email:
Web: www.thinknicity.com
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Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
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Associate Director / Director of Biostatistics - Mountain View, CA
Job Number: F1481
Fulltime position
Job Description:
The Associate Director/Director will ensure that appropriate analysis procedures are used,
and that final reports effectively describe statistical methods and results of analyses.
Administrative responsibilities will include direction of the Biostatistics group within the
Department of Biostatistics at the given location, recruitment and training of statistical personnel,
conduct of performance reviews, and assistance with preparation of the Department's budget.
Candidate Requirements
The successful candidate must possess a PhD in Statistics or Biostatistics
Must possess 5 to 10 years of clinical trial design and analysis experience.
Qualified applicants should have supervisory experience and extensive knowledge of clinical
trials methodology, regulatory requirements, and statistical software.
Interpersonal skills to motivate and direct activities of senior-level staff and good
communication skills are essential.
Responsibilities will include oversight of statistical input to clinical study design,
analysis plans, statistical analyses, and reporting.
Clinical SAS Developer/Analyst - Mountain View, CA
Job Number: F1487
Fulltime position
Job Description:
The successful candidate will develop and support fully validated applications in
accordance with a pre-defined systems development life cycle.
Additional responsibilities to include the development, maintenance, and validation
of code to create tables, listings, and figures for the analysis and reporting of clinical trial data.
Individual will also develop and maintain department documentation; system documentation,
SOPs, work processes, etc.
Must be able to adequately and appropriately communicate with management and/or other
departments as to requirements and timelines.
Individual will be responsible for other duties as assigned.
Candidate Requirements
The successful candidate must possess a Bachelor’s degree in computer science, mathematics, or related field.
Must have a minimum of 5 years of experience performing analysis and reporting of clinical
trial data using SAS, preferably in pharmaceutical industry setting.
Minimum of 3 years applications development experience using SAS and SAS/AF in a UNIX environment.
Must also possess demonstrable knowledge of computer systems development life cycle.
Job Opportunity in Baltimore, MD
Full-time permanent position for an experienced SAS Programmer Analyst
is available in the Credit Policy department of CitiFinancial in Baltimore,
Maryland.
Great location -- just a few blocks north of Baltimore's Inner Harbor.
The selected individual will be responsible for developing and producing sophisticated
SAS programs on IBM mainframe (MVS) and pc (Windows) platforms to monitor credit risk,
identify high risk branches, manage data for score card development, conduct acquisition
analyses, clean and validate data, and produce exception and field reports. Additional
responsibilities are to provide support for credit management projects and to provide
SAS training and support.
This position requires a BS/BA degree in a quantitative field such as mathematics,
economics, demography, statistics, life sciences, or physical sciences. Advanced
degree is preferred. Must also have two (2) years experience in a position using
SAS programming in quantitative analysis. Must have excellent SAS programming skills
including program design, testing, documentation, implementation, operation, and
maintenance. Additional factors include a working knowledge of lending and credit
policies, personal computer, mainframe computers, managing large data files (greater
than 1 million records), strong analytical and problem-solving skills, the ability to
communicate effectively in writing and speech, and handling multiple programs in a
production setting.
Applicants must be eligible to work in the United States.
Send resume and salary requirements no later than June 30, 2002 to:
Helen-Jean Talbott
CitiFinancial
300 St. Paul Place, BSP10A
Baltimore, MD 21202
FAX: (410)332-2838
Email:
Senior Analysis Programmers: Philadelphia and Virginia
PRA International is a Contract Research Organization with Offices around
the world. This posting is for our Charlottesville VA and Horsham PA Trials
Management Centers. We're looking for bright, energetic SAS programmers with
proven team skills and a desire to work in clinical trials. We offer exposure
to Oracle, SAS, Core Dossier, Documentum, and to Clinical trials work. Of
course, significant exposure to these fields of knowledge is highly desirable,
but not necessary. We strongly support certification, conference participation,
and career growth. The pay is great. Get in touch.
Lee Walke
Director, Analysis Programming
PRA International
4105 Lewis and Clark Drive
Charlottesville, VA 22911-5801 USA
Email:
Web: www.praintl.com
(434) 951-3208 (direct)
(434) 531-3208 (mobile)
(434) 951-3001 (fax)
31610 (Nextel Direct Connect)
Global Search Recruitment Systems, Inc. is looking for qualified technical professionals for the
positions below. We specialize in placing SAS programmers and Statisticians
at all levels.
You MUST have pharmaceutical experience for these positions. If you are a
green card holder or US Citizen please reply to:
Barry Rosen
Global Search Recruitment Systems, Inc.
Phone: 1-800-652-5122x301
Fax: 973-781-1999
Email:
Web: www.gsearch.com
The following positions are all with Major Pharmaceutical Corporations in
New Jersey and New York areas.
Senior Biostatistician I/II, Full time and Consulting
Job Description
Review protocols & case report forms for soundness of the trial design
Write statistical methodology section of the protocol
Prepare analysis plan and computer programs
Analyze data, write the statistical section of the clinical trial report, and review clinical trial
report
Participate in drug project related activities
Detail Info
3 years Education Masters Degree
M.S. in Statistics with at least 3 years of related
experience or Ph.D. in Statistics with limited or no experience for Senior
Biostatistician I M.S. in Statistics with at least 6 years of related
experience or Ph.D. in Statistics with at least 3 years of experience for
Senior Biostatistician II
Knowledge of the SAS computer package
Some knowledge of clinical trial methodology
Good oral and written communication skills
Strong statistical skills
Knowledge of FDA statistical guidelines
Knowledge of drug development process.
Sr Biostatistician
Responsible for statistical methodology and statistical analysis plans for
clinical studies as a member of the biostatistics team. Ensures that
activities and processes performed are conducted according to company and
sponsor requirements. This position works closely with the biostatistics and
data management departments on various clinical projects.
Act as lead Statistician on complex trials and across multiple studies.
Act as a lead representative of the biostatistics department on project
teams. Attend project team meetings as necessary.
Meet with sponsors as requested during protocol development to ensure
adequacy of proposed study designs with respect to statistical feasibility.
Write statistical methodology sections of individual protocols. Write
formal Statistical Analysis Plans to be carried out in the analysis of
clinical studies.
Perform statistical analyses of data and interpret results to ensure
validity of conclusions. Meet with sponsor as requested throughout trial to
discuss progress of clinical studies.
Interact with data management personnel as necessary to ensure that
datasets are in usable format; perform statistical diagnostics prior to
database locking.
Interact with SAS Programmers to ensure that appropriate programs are
being developed for current clinical studies.
Perform statistical quality assurance review and program validation for
each project.
Interact with medical writers in production of statistical and
integrated clinical/statistical reports and other documents containing
statistical information. Review statistical sections of draft documents.
Interact with other departments, such as clinical operations and
project management, to ensure a high level of client satisfaction through
successful execution of projects.
Qualifications
MS degree required with a minimum of five years experience in statistics or
PhD with two years of experience in statistics Ability to work in a
fast-paced, team-oriented environment Computer proficiency is required
Ability to perform statistical analyses of clinical data Ability to define
problems, collect data, establish facts, and draw valid conclusions Ability
to interpret an extensive variety of technical instructions in mathematical
or diagram form and deal with several abstract and concrete variables
Ability to interpret results of data analyses to ensure validity of
conclusions Ability to read, analyze, and interpret common scientific and
technical journals Excellent interpersonal communication skills (written and
verbal) Strong attention to detail Excellent time and resource management
skills
Senior Staff Biostatistician
Job Description
Review protocols & case report forms for soundness of the trial design
Write statistical methodology section of the protocol
Prepare analysis plan and computer programs for inferential analyses
Analyze data, provide statistical sections and input for preparation of clinical trial reports
Take statistical lead in publication support and interaction with external experts
Take statistical lead in drug project related activities including design of clinical development programs
Take statistical lead in support of new drug submission/approval
Oversee CRO deliverables for trial contracted out
Experience 9 years
Education PhD
Requirements
M.S. in Statistics with at least 9 years of related experience
or Ph.D. in Statistics with at least 5 years of experience for Senior Staff
Biostatistician
Good knowledge of the SAS computer package
Good oral and written communication skills
Strong knowledge of clinical trial methodology
Strong statistical and data analysis skills
Good knowledge of FDA statistical guidelines
Excellent knowledge of drug development process
Strong project management skills
Sr. Staff Biostatist/Asst. Dir
Job Description
Review protocols & case report forms for soundness of the
trial design
Write statistical methodology section of the protocol
Prepare analysis plan and computer programs for inferential analyses
Analyze data, provide statistical sections and input for preparation of
clinical trial reports
Take statistical lead in publication support and interaction with external experts
Take statistical lead in drug project related activities including design of clinical development programs
Take statistical lead in support of new drug submission/approval
Oversee CRO deliverables for trials contracted out
Experience 8 years
Education PhD
Minimum Requirements
Grade 10: Ph.D. in Statistics with at least 8 years of experience of extensive experience in Pharma industry
Grade 9: M.S. in Statistics with at least 9 years of related experience or Ph.D. in
Statistics with at least 5 years of experience for Senior Staff Biostatistician.
Strong knowledge of the SAS computer package
Excellent oral and written communication skills
Strong knowledge of clinical trial methodology
Strong statistical and data analysis skills
Excellent knowledge of FDA/EU statistical guidelines
Excellent knowledge of drug development process
Excellent project management skills
Direct experience with FDA/EU Authority
Participation in international clinical team(s) as a lead statistician
Contact:
Barry Rosen
Global Search Recruitment Systems, Inc.
Phone: 1-800-652-5122x301
Fax: 973-781-1999
Email:
Web: www.gsearch.com
If the position is a contract, we work with contractors on a temporary
W2 basis, or with Incorporated entities, provided the nature of the work meets the
qualifications that will allow the use of an Independent contractor as defined by the IRS.
Contact:
Heather Brown
Technical Recruiter
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
Email:
Web: www.thinknicity.com
**************************************************************
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
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Director of Bio Statisticians - Palo Alto, CA
Order F1476
Full-time position
Our process of conducting face-to-face interviews before presenting candidates to our client means we can work with local Bay-Area candidates only
Currently, relocation expenses are not available for this position
Currently, our client is unable to offer a visa transfer or sponsorship
This position will not accommodate third party or agency representation
Job Description:
Provides direction to Bio Statisticians and analytical program analysts based on general statistical and programming principles, departmental policies, organizational goals/objectives and corporat
Perform supervisory and management functions relating to the administrative and scientific activities of staff in department of Bio Statistics.
As a formal member of a cross-functional clinical drug development team, plan and implement clinical drug development programs that efficiently deliver approvable registration packages for marketa
Provide appropriate study design, analysis planning and valid analysis and reporting of clinical study results.
Essential functional duties of the position.
Provide leadership to the department, execute corporate goals and objectives in a timely and quality manner, and provide strategic leadership and vision to the departmental staff.
Represent Bio statistics department in project planning and senior or corporate level meetings; identify mission critical needs of the departments.
Contribute to the implementation and execution of the drug development plan, and assist in the creation of strategic objectives for NDA filing.
Responsible for departmental resource management, capacity analysis, benchmarking and metrics, and establishing SOP and guidelines/procedures.
Formally supervise the activities of analytical program analysts and statisticians. Perform annual evaluations for direct reports, proactive in solving issues and establishing departmental perfor
Support professional activities, promote job satisfaction, encourage training, and provide training and consultation about statistical methodology and statistical programming techniques.
Assume primary statistical role in creation of registration documents, and in interactions with regulatory agencies.
Provide optimal strategy for clinical drug development programs in a written clinical development plan, establish individual clinical study plan synopses, establish and ensure the use of standards
Independently develop statistical methodology appropriate for the analysis of clinical studies utilizing knowledge of regulatory agency/statistical guidelines and of the statistical literature.
As a member of clinical project team, provide optimal study design, analysis planning and appropriate analysis and reporting of clinical study data.
Assist in the design of case report forms and the selection of study data validation software by providing an analysis and reporting perspective within the team.
Write analysis plans and statistical reports. Participates in the review and development of joint clinical/statistical reports.
Other responsibilities.
Provide consultation and advice to Biometrics staff assigned to other programs.
May work on multiple clinical project teams (Phase I - III, or IV) simultaneously.
Also need to oversee multiple teams of statistic (including in-house statisticians and program analysts as well as CROs).
Knowledge/Skill Requirements
Ph.D. in Statistics, Bio statistics, Mathematics or related field with 8+ years related experience in pharmaceutical or biotechnology industries or MA/MS with 10 years experience.
Experiences should also include 6+ years with regulatory contacts, 4+ years in the management of external technical resources, and 4+ years in direct supervisory experience.
Thorough knowledge of drug development process and relevant FDA regulations.
Experience with clinical data systems, analysis process, submitting and supporting regulatory agency review of registration package.
Ability to understand and apply statistical methodology appropriately to the design, analysis and reporting of clinical studies.
Ability to identify areas of statistical research useful for improving the analysis and reporting of clinical study data. Ability to independently develop such statistical methodology and apply i
Skilled in the use of computers and statistical analysis software.
Demonstrated professional excellence through publication, presentation, and external recognition.
Demonstrated skills in direction, management of both internal and external resources (which includes providing & reviewing analysis/programming specifications), mentoring, and staff development (e
Demonstrated skills in leadership, influence, facilitation, assertiveness, consensus building, and interaction.
Ability to make sound judgment and exercise discretion.
Willingness to accept responsibility/accountability and is self-motivated and initiative.
Demonstrated ability to effectively communicate with regulatory agency staff and advisory committees.
Proven skill of excellent presentation, oral and written communication.
Demonstrated proficient project management, time management, recruiting and resource skills.
Other
Proven performance of required tasks, as evidenced in outstanding performance in current tasks and/or documented record of accomplishments.
Evidence of strong supervisory skills, as shown through management of multiple projects and staff members.
Excellent written and verbal communications skills.
Good organizational skills with the ability to adapt and adjust to changing priorities.
Positive attitude and the ability to work well with others.
Data Quality Assurance for Clinical Data Management - Emeryville, CA
Order F1474
Fulltime position
Currently, relocation expenses are available for this position
Our client is in a position to offer a visa transfer or sponsorship
This position will not accommodate third party or agency representation
Job Description:
Perform the primary function of the Data Quality Assurance group
This entails
- Auditing the hardcopy (Case Report Form, laboratory Electronic Data Transfer, Data Clarification Forms, and other study-specific documents) against associated database records for all clinical stu
- Report back to the study teams as well as senior BCDM and Clinical Operations staff on the results thereof via DQA's QC and QA report templates.
- Assist Clinical Data Coordinators (CDCs) during the study initiation and database setup phase of their respective clinical studies by reviewing the first draft of the Quality Specifications docume
- Perform Post Database Lock Changes and e-extraction of SAS datasets per written request by Bio statisticians.
- Assist in maintenance of the library of standard rules for all database panels associated with the client’s generic standard Case Report Forms (CRFs).
- Assist in the annual review and regular update of all documents (checklists, guidelines, forms) owned by the DQA functional area.
- Help provide training on the DQA function as well as BCDM documentation for all new BCDM (as well as Clinical Development and Vaccines) personnel.
- Assist in and make presentations on DQA functions and related areas of interest to personnel both internal and external to Assists with other (B)CDM projects (e.g., computer system validation proj
Candidate Requirements
B.S. degree, 3+ years previous Clinical Data Management experience in the pharmaceutical or biotechnology industry is required.
Background in relational database use, medical terminology, and strong interpersonal and problem-solving skills are essential.
Bio-Statistician - South San Francisco, CA
Order F1412
Fulltime position
Local Bay-Area candidates only please
Currently, relocation expenses are not available for this position
Currently, our client is unable to offer a visa transfer or sponsorship
This position will not accommodate third party or agency representation
Job Description:
Work with senior bio-statistics staff and clinical development teams in the design and conduct of clinical studies and in the evaluation, interpretation and preparation of study results.
For assigned projects, provide sound experimental design and data analysis expertise.
Author the protocol statistical analysis sections and generate study randomization.
Determine analysis and data presentation specifications for programmer analysts and statisticians.
Perform analysis, interpret study results, and collaborate with medical and bio-statistics staff to produce interim reports, final reports, and publications.
Represent the bio-statistics function on project teams.
Interact with FDA staff to ensure drug project studies meet FDA requirements.
Attend meetings with FDA to ensure ongoing agreement on project development.
Work with bio-statistics and clinical staff to define datasets and analyses for the Integrated Summary of Safety and Efficacy.
Interpret results of integrated summary analyses and collaborate with medical and bio-statistics staff to produce reports for the application to the FDA.
Candidate Requirements
Minimum requirements: A Ph.D. in Bio-statistics or closely related discipline with a minimum of two years experience, or a Master's Degree in Bio-statistics with a minimum of four years experience
Must possess a comprehensive and detailed understanding of statistical experimental designs and analyses, clinical trial requirements and statistical software packages such as SAS and S-PLUS.
Strong interpersonal and effective communication (oral and written) skills.
Pharmaceutical industry or closely related experience required.
Experience with the management and statistical analysis of data obtained from Phase I - III clinical trials or studies in support of U.S. PLAs/NDAs.
Senior Statistical Programmer Analyst - South San Francisco, CA
Order C10226
Contract position
Contract Length: 6 months
We work with contractors on a temporary W2 basis, or with Incorporated entities, provided the nature of the work meets the qualifications that will allow the use of an Independent contractor as de
This position will not accommodate third party or agency representation
Job Description:
As a member of a clinical project team, the Senior Statistical Programmer Analyst plans, designs, develops, implements, and maintains software for the monitoring, reporting, and analysis of clinic
Develop and execute SAS and other software to support analysis requests by pharmacokinetic (PK) scientists.
Create statistical files for Bio-Statistical analysis.
Provide consistency across protocols within a project on CRFs, database design, analysis files, and tables, listings, and graphs.
Test, document, review and verify all programs according to department guidelines.
Develop specifications and code for new standardized PK software to help facilitate performing maintenance, analysis, and reporting of clinical and PK data, as needed.
Provide data in SAS transport files, and other appropriate deliverables and documentation for internal customers, regulatory submissions, or external customers.
Communicate effectively.
Work with minimal supervision.
Responsible for broadly defined goals.
Candidate requirements:
Advanced skills in SAS programming language, especially data step programming and report writing. Experienced in macro writing.
Knowledge of advanced statistical procedures in SAS, e.g., LIFETEST, MIXED, GLM.
Skilled in the use of graphics software, e.g., SAS/GRAPH, S-Plus.
Understanding of programming standards and accepted software development techniques.
Some knowledge of PK analyses and parameters.
Good interpersonal skills.
Good verbal and written communication skills.
Experience with desktop tools.
Ability to work on multiple tasks simultaneously and meet project deadlines.
Demonstrated ability to interact confidently with members of other functional areas in clinical and/or scientific teams.
A working knowledge of basic statistics for communicating effectively with Bio-Statisticians and scientists.
Understanding of regulatory guidelines that affect statistical programming deliverables.
Experience using SAS to process, report, and analyze clinical trial data.
Understanding of the drug approval process.
Experience interacting with others for defining and implementing user defined reports.
Effective in working in teams and communicating one-on-one and with groups.
Extensive experience in the support of at least one phase of drug development.
Participation in PK analysis work would be a plus.
Experience with UNIX and MS/Windows and with transferring information between them.
Education and training
A minimum of 4 years of SAS programming with a BS in statistics, math, computer science, or equivalent experience, or 2 years with an MS in a related field
Bio-statistician II or Senior Bio-statistician - South San Francisco, CA
Job Number M1414
Fulltime position
Job Description
The Senior Bio-statistician will have full responsibility for specific segments of major clinical projects.
The position is directly responsible for the statistical integrity, adequacy and accuracy of the clinical studies/projects.
You will plan, coordinate and provide statistical analyses, summaries and reports of studies in support of product development and US PLAs/NDAs.
You will provide appropriate statistical advice and support to the clinical directors.
Your advice should be consistent with the prevailing standards of good statistical methodology, regulatory guidelines and departmental guidelines.
Candidate Requirements
Must have at least two years experience with a drug development company with experience in NDA submissions to the FDA.
A Ph.D. in Bio-statistics or closely related discipline.
A minimum of 4 to 5 years experience or a Master's Degree in Bio-statistics with a minimum of 6 to 8 years experience in the support of clinical studies,
preferably in a pharmaceutical industry or clinical studies unit setting.
Demonstrated sound knowledge of applied statistics and bio-statistics and relevant experience
in the applications of statistics to medical trials.
Experience with major statistical software packages such as SAS and S-plus.
Strong interpersonal and effective communication (oral and written) skills.
Pharmaceutical industry or closely related experience required.
Experience with the management and statistical analysis of data obtained from Phase I-III
clinical trials or studies in support of US PLAs/NDAs.
Senior Manager, Clinical Data - Palo Alto, CA
Job Number F1477
Fulltime position
Job Description:
Our client is currently seeking a Senior Manager in their Clinical Data Management department.
In this role you will manage CRO data management support for clinical trials utilizing paper
CRF's and support trials utilizing electronic CRF's.
Direct responsibility and/or management of CROs and/or department clinical data managers with
respect to: development of data management plans, database and edit check specifications, coordination
with clinical operations in the development of CRFs, coding, query resolution, data lock procedures,
management of timelines, and identification of timeline risks.
You will also support the development of department SOPs, guidelines, and supporting templates.
Candidate Requirements
This position requires a minimum BA/BS degree
Minimum 6 years experience in clinical data management required.
Knowledge/Skills: clinical trial data/databases; SAS; adverse event and medication coding
(COSTART and/or MedDRA, WHO-DD)
Ability to manage and optimize CRO and/or EDC vendor relationships is expected.
For more Info,
Contact:
Heather Brown
Technical Recruiter
Thinknicity, LLC
5 Third Street, Suite 500
San Francisco, CA 94103
415 247 7700 Ext. 226 Tel
415 247 7755 Fax
Email:
Web: www.thinknicity.com
Manager of Analytics (eCRM) - US-CA-Los Angeles
My client is searching for a Manager of Analytics for their HQ in
Los Angeles, CA. Relocation is provided for.
Responsibilities:
This is a leadership position, responsible for leading high-level
modeling for the data warehouses and CRM initiatives for Ticketmaster
and potentially its core business units (citysearch.com, Match.com,
ReserveAmerica.com, Evite.com, etc.). This position is responsible for
CRM analytics as a whole.
Responsibilities will include:
60%: Develop high-level targeting and segmentation models inclusive
of campaign management
15%: Execute ad-hoc analytical projects, including customer-level analyses,
segmentation analysis, product affinity and customer profiling analysis, etc.
15%: Evaluate campaign strategy development, targeting, selection,
campaign test and measurement design and post-campaign analysis
10%: Interdepartmental communications: Work with internal marketing,
executive management, development teams for needs gathering, guidance,
and leadership for data analytics direction and goals.
Qualifications:
BA/BS degree in Statistics or a related discipline (e.g., Mathematics,
Computer Science with heavy course load in statistics).
3+ years progressive business experience in database marketing or related
fields
Proven experience with research, statistical analyses, and programming
utilizing a variety of multivariate statistical techniques including
regression,
factor analysis, cluster analysis, conjoint, etc.
Experience working with, or exposure to, campaign management, data mining
and statistical modeling tools (e.g., Epiphany, MapInfo, SAS, etc ) and
consumer databases. Campaign management experience is a pre-requisite for
this role.
Experience developing targeting models (e.g., regression, CHAID, etc.) and
individual-level segmentation
Strong strategic thinking, communication and analytical skills
Client-service and/or consulting experience a plus.
Frank Scannello
Hire Efficiency
Email:
Web: www.hirefficiency.com
904-543-0808
SAS Programmer needed for Connecticut-U.S.-(Recruiter)
Tech Associates (Information Systems recruiters) is recruiting for a
Informatics Analyst (SAS) Professional for:
Connecticut.
Must have five plus years of SAS programming experience on
Mainframe & PC, three plus years of Health Insurance experience and be expert in US Quality Algorithms,
data mining and demographic analyses.
Salary is from $55,000-$70,000 depending on experience. Reasonable relocation expenses are available.
Salary depends on length of experience, specific application experience and level of education. This
is a permanent job and the client will not sponsor! NO H1-Bs, TN-1s!
Must be a U.S. citizen or have a Green Card and currently reside in the U.S. by client request.
Please E-Mail a resume by RTF or Microsoft Word attachment to:
Mike Sigman
Tech Associates
Email:
Toll Free Voice: 888-870-7212
Programmer - Washington, DC
APCO Insight, the opinion research and message development division of APCO
Worldwide, is seeking experienced programmers in statistical software
(STATA, SAS, SPSS) for contract work. APCO Insight has developed a
proprietary brand research model and needs the assistance of a programmer to
help design customized programs in a statistical software package to
manipulate data and perform specialized statistical analysis. Specifically,
we need a program to perform the following functions:
Compute factor means for individual brands that are standardized to the
overall factor mean of all brands in the dataset.
Compute factor means for individual brands by discrete subgroups that are
standardized to the overall factor mean within the subgroup.
Compute confidence intervals based on standardized means.
Compute regression coefficients and standardize individual regression
coefficients to the mean of a series of coefficients.
Order the standardized factor means and standardized regression
coefficients from highest to lowest coefficient.
Export ordered data into Excel.
Produce specialized charts.
Email:
assist us in developing this program. We would like to have this program
developed by August 1.
Bryan G. Dumont
Vice President
APCO Insight
1615 L Street, NW
Suite 900
Washington, DC 20036
Web: www.apcoinsight.com
(202) 778-1486 Tel
(202) 466-6002 Fax
(703) 582-9418 Cel
Email:
Chrystine Gilchrist
APCO Insight
1615 L St, NW
Washington, DC 20036
202.778.1093
202.778.1478 (f)
202.270.4056 (c)
Email: