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Statistician Position in San Francisco (San Carlos, CA)
Position: Statistician
Location: San Carlos, California
Reports to: Director or Manager of Analytical Operations
Please send resume to
David Davtian
Email:
Overview
DemandTec offers a breakthrough pricing and promotion optimization
service for e-commerce and traditional retailers that allows them to
identify optimal pricing and promotion combinations for their
products. The service uses sophisticated analytical techniques to
optimize price and promotion as a single system, taking into account
the interdependencies between both complementary and substitute items.
The Operations Department has the primary responsibility to ensure the
consistent and reliable operation of the processing functions that
support the corporation's products and services. Statisticians within
Operations at DemandTec execute statistical analyses in a production
environment, and collaborate in the development and enhancement of the
econometric modeling engine. The ideal candidate will have extensive
experience with constructing SAS datasets from a variety of customer
data sources, developing an understanding of that data through the use
of SAS tools, presenting data to end-users using SAS reporting tools;
experience in list management (merging, sorting, matching, creating
extracts and reformatting) in a large dataset environment is
essential&; running pre-defined statistical models, and analyzing
modeling results prior to delivery to end-users.
Responsibilities
Develop an expert understanding of the existing modeling
infrastructure and process
Develop an expert understanding of the relationship between the
econometric modeling and decision support application databases
Write customer-specific code to read data from a variety of sources;
create analysis datasets; execute, summarize, and communicate analyses
Perform ad-hoc analysis of results to support multifunctional team
(Professional Services, Sales, Science)
Collaborate on the research and development of future methodologies
and products
Identify and assist in the implementation of process improvements
Minimum Requirements
MS in Statistics preferred; will consider MS in Operations Research or
BS in Math/Statistics
1 to 3 years prior work experience
Demonstrated analytical skills and great comfort with handling vast
quantities of data
Strong SAS programming skills
Experience in working with large datasets for list management:
merge/purge, data extracts and reformatting, sorting, matching
Knowledge of PROC MEANS, SUMMARY, FREQ, SQL
SAS contract opportunity in Dallas, TX
Must have strong AIX knowledge and scripting skills. Must have strong
DB2, or have strong SAS Macro coding and be familiar with SAS/Access
and SQL.
Should have the following:
a) MVS OS/JCL
b) SAS/AF
c) SAS/Connect
Client/Server a plus.
Dennis Osha
Email:
2 SAS Job Postings: E-sub specialist, and PK programmer - San Francisco, CA
1: E-SUB SPECIALIST w/ PHARMA in SAN FRAN. COMP $100K+
As a member of the electronic submissions team, the Senior Statistical
Programmer Analyst (SPA) for Electronic Submissions facilitates the
preparation of data, data documentation, computer programs, report
documents, and case report forms for electronic submission of clinical
studies to the FDA. The Senior SPA provides leadership on software and
process approaches, as well as general strategy.
2: SAS PROGRAMMER WITH PHARMACOKINETIC EXPERIENCE IN SAN FRAN. COMP $100K+
Regular SAS Programmer Analyst skills like those above: SAS data
step, statistical procedures, report writing macro code; data
checking; working well in teams. Experience with PK data analysis.
Exposure to biochemical assay systems, laboratory information
management systems, and/or toxicology data.
Some math skills, such as calculation of area under curve.
Contact:
Julie, Statistical
Recruiter, ASG.
Email:
800.279.8082 x131
SAS System Analyst - Opportunity in the USA; Ann Arbor, Michigan
Below is a position in the pharmaceutical industry I am recruiting for.
If you are interested in more information please attach your resume to
an email and send it to me.
Best regards,
Ken Schmidt
Computer Contract Services, inc.
734-484-7777
Email:
System Analyst/SAS Programmer
Requirements:
SAS Experience: Must have a minimum of 3 years of business related SAS
programming experience (academic experience can not be included as part
of this minimum requirement). This experience must include designing
and coding programs from design concept and not merely modifying or
executing existing programs.
SAS Version: Must have experience with SAS Version 6 or above.
SAS Macros: Must have experience creating complex and reusable macros.
Further, must be able to pass parameters and able to test and debug
self-developed macro code.
SAS Procedures: Must be proficient with Base SAS procedures including
but not limited to: freq, report, tabulate, sort, print, transpose,
summary and means.
SAS Custom Reporting: Must be proficient at creating custom reports
using data_null_ and put statements.
SQL: Must be proficient with SQL and be able to create data sets and
macro variables.
Systems Development Life Cycle: Must be experienced with all phases of
software development including gathering requirements, creating
specifications, developing code and validating programs.
Platforms: SAS experience must include Unix and NT platforms.
Excel: Must be proficient in the use of Microsoft Excel.
Communications: Must be able to work effectively in a team environment
and be able to receive instructions and convey related problems and
issues.
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
Clinical Data Coordinator
Contract position is in Mountain View, CA
Order 10223
** Currently, relocation expenses are not available for this position **
** Currently, visa transfer/visa sponsorship is not available for this position **
** 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 def
** This position will not accommodate third party or agency representation **
Job Title: - Clinical Data Coordinator
Job Description:
As Clinical Data Coordinator in the Department of Statistics & Data Management, you will work closely with clinical research associates, statisticians, clinicians, and personnel from other discipl
Your main responsibility is to coordinate data management activities including creation of the data capture instruments, the database definition, data input, database maintenance and database rele
You will also manage contract data management vendors when work is outsourced under guidance of management and/or study operating team and coordinate the review and approval of database definition
Candidate requirements:
BA/BS or equivalent, preferably in computer studies, biological science, physical, health or social sciences
2 years experience in clinical data management is required.
Must be proficient in Windows, Unix environment and other database software systems and have data handling experience coupled with demonstrated ability to apply and understand database management
Some Clinical Trial experience and knowledge of SAS is a plus.
Experience with DATA FAX is a major plus.
A 4 Year Degree id required
Contract Length: - 6 months
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
SAS/Internet Architect - Bureau of Labor Statistics in Washington, DC
We (User Technology Associates, Inc.) are looking for a Sr.
SAS/Internet Architect to support development initiatives at the Bureau of
Labor Statistics in Washington, DC.
The ideal candidate must have experience delivering systems using
SAS/Internet and complementary technologies, such as Java and Perl. Must be
familiar with architectural options and trade-offs associated with very
large-scale statistical survey data processing systems, including solutions
that do not include SAS. Must be capable of growing the competence of a team
of SAS developers. Ten years of SAS experience required. Technical
environment includes SAS/Internet, SAS/AF, Sybase, Unix, Windows NT.
If you are interested, then please send you resume to
Email:
Posted by Bryan
MS Stat Grads: Clin SAS Programming Position - RTP, NC
I'm looking for a rising star - a MS Stat grad with strong
SAS skills to come join a growing CRO in RTP, North Carolina. You
must have excellent communication skills and superb SAS skills. This
is a *golden* opportunity to break into the clinical research SAS
arena. Comp is $45K-$50K + benefits. No relocation will be provided.
It is a long-term contract. I work five offices down from their
Director, and this opportunity will go by FAST.
Send resume to:
Julie Daves
ASG Recruiter
Email:
800.279.8082 x131
Health Care Analyst (Data Analyst)- Columbus, OH or Easton, MD Office
JOB POSTING
April 11, 2002
Delmarva Foundation for Medical Care is a highly successful and rapidly
growing not-for-profit company with a passion for excellence and over 25
years of experience in health care. Seeking Health Care Analyst experienced
in using/analyzing health care data. SAS or SPSS experience required.
Managed care, quality improvement, Medicaid, or social/rehabilitation
services experience desirable. Knowledge of applicable medical coding such
as ICD-9-CM and CPT a plus. Bachelor's degree 3-5 years experience or
masters degree with 1-2 years experience preferred, preferably in
healthcare, statistics, or a related field within the healthcare industry.
The successful candidate must be willing to travel up to 25 percent time.
Visit us at www.dfmc.org Attractive benefits and
compensation package with opportunity for professional growth. Affirming
equal opportunity in principle and practice.
For immediate consideration, please submit resume with salary requirements
to corporate headquarters:
Health Care Analyst, State Programs
Delmarva Foundation for Medical Care, Inc.
9240 Centreville Road, Easton, MD, 21601
Fax: 410-822-5032
Email:
Posted by Timothy Champney
Email:
3 SAS Opportunities
We are looking for Senior SAS consultants. We currently have three long term
needs. They are as follows:
SAS Developer Lead
Qualifications:
8+ years current SAS experience, including database design and
Reporting
Experience with regulatory filings and/or compliance issues
Current experience with Windows 2000, MS Access, SQL queries
Experience with Perl a plus
Working knowledgeable of SDLC
Well-developed analytical skills
Organized, detail-oriented, quality-driven
Excellent communication skills
Reporting Lead
Qualifications:
5+ years current SAS experience, including database design and
reporting
Experience with regulatory filings, compliance issues, validation and
QC tasks
Current experience with Windows 2000, MS Access, SQL queries, MS Excel
(macros, pivot tables)
Management experience
Working knowledgeable of SDLC
Well-developed analytical skills
Organized, detail-oriented, quality-driven
Excellent communication skills
Reporting QC and Validation
Qualifications:
3-5 years current SAS reporting experience
Experience with regulatory filings, compliance issues, validation and
QC tasks
Current experience with Windows 2000, MS Access, SQL queries, MS Excel
(macros, pivot tables)
Well-developed analytical skills
Organized, detail-oriented, quality-driven
Willingness to do whatever is necessary to deliver the survey results
If you are interested or know anyone who would be, please contact
Megan
Email:
or call 888-562-5945
The Hired Guns (www.thehiredguns.com)
Allison B. Hemming
The Hired Guns
27 West 20th Street
Suite 1003
NYC, NY 10011
Telephone: 212-366-1918
Fax: 212-366-6703
SAS/SQL DATA MINING GURUS WANTED FOR GLOBAL SECURITIES FIRM - NYC
OVERVIEW:
Title: Data/Business Analyst
Positions Open: 2
Type: Medium Term Assignment (very high chance of leading to permanent
position).
Rate: Project fee to be discussed if selected for interview process
Interviews Begin: ASAP
How to Apply: Read project description in its entirety and follow the
instructions
If statistical analysis, data mining and business analysis are
YOUR buzz words, read on. The Hired Guns is working with the
marketing group of a top tier securities firm to hire up to two
Data/Business Analysts. The day-to-day role for this position would require
you to work on projects that typically involve data access, data
manipulation, data analysis, synthesis and interpretation/presentation of
business implications. If you're passionate about helping companies figure
out where opportunities exist, who they should be targeting and why, you
should apply for this position. If you live for data -- this gig's for you!
SPECIFIC RESPONSIBILITIES INCLUDE:
Identifying opportunities to increase client profitability and improve
client satisfaction by mining data from the firm's Marketing Database (which
is made up of various internal databases).
Employing various data mining techniques including: client profiling
analysis, market segmentation and querying client centric data to gather
relevant data for analysis.
Interpreting strategic implications and results of data and business
analyses.
Summarizing findings and results into presentations for senior management.
Supporting Senior Database Marketing and Client Analysis team members in
various ad hoc projects and analyses.
QUALIFICATIONS:
Masters Degree in Statistics, Applied Math, Economics or Computer Science
and 1+ years work experience
-OR-
Undergraduate Degree and two to four years of business experience.
Preferably quantitative in nature (statistics, applied mathematics,
economics, finance, computer science, etc.)
- AND -
Strong competency using SAS and SQL to gather and use data from relational
databases.
High level of proficiency using tools such as Microsoft Excel and Access
to pull and integrate data from multiple sources.
Knowledge of Oracle and Sybase a plus. (Note: programming not required.)
Excellent academic performance
Direct Marketing experience a plus.
Must have an inquisitive nature.
Must be project oriented and be able to meet deadlines.
Strong oral and written communication skills.
Must work well in a team-oriented environment.
Knowledge of the securities industry a plus.
Financial reporting experience a plus.
Excellent references from managers who can discuss your capabilities.
Exceptional organizational skills.
HOW TO APPLY:
- Please be sure that you meet the qualifications listed above before
responding.
- Next, in the body of an email, please send us a cover letter that
outlines what types of database work you have done and what programs you
have used.
- Please attach a copy of your resume and your cover letter to the email
(we generally forward this on to the client)
- Please email all cover letters and emails to the Big Gun,
Tara Lynch at:
Email:
No fax or phone calls please. Due to the narrowly defined objectives and
criteria established by the client, only candidates with experience related
to this project will be considered.
Senior Statistical Analyst (2) - Dallas, TX
SUMMARY :
The selected person will be responsible for developing and building complex statistical models
as a member of a team in the support of client business initiatives, ensuring solutions are consistent
with organization objectives and overseeing the development and empirical/methodological
foundations of analytical tools that support various departments. Must use SAS.
Pricing Role:
This position will emphasize the Pricing, Forecasting and Marketing Mix problems of the department.
The concentration will be on defining pricing guidelines for the stores and you will be tapped with
forecasting and defining the business metrics that help make the decisions by which the company
will be run. Must know how to do time series forecasting models.
CRM Role:
This position will emphasize defining CRM metrics for the company. These include but are not limited to
lifetime value (LTV), customer potential, customer scorecard, and analytical segmentation work.
Requirements:
The selected person should have 3 years in applied quantitative research environment. She/He will work on a
team that builds statistical models to support client business initiatives. The selected person will oversee the
development and empirical/methodological foundation of analytical tools that support various departments not
limited to Product, Finance, Marketing and CRM. This person will also interact with other divisions and departments
regarding research approach, data availability and analysis results and communicate results. The selected person
should have a Masters in Statistics, Applied Mathematics, or related field.
For consideration, please email your resume to:
Tom Hull
Partner
mangieri/solutions
1 Riverside Road
Sandy Hook, CT 06482
Phone: (203) 270-4800 x101
Fax: (203 270-4815
Email:
Web: www.mangierisolutions.com
12 East 41st Street, 9th Floor
New York, NY 10017
Phone: 212 545-8511
Fax: 212-545-8520
Website: www.analyticrecruiting.com
Email:
Direct Marketing Data Analysts - Washington D.C.
Strong SAS and data analysis experience required for junior level positions
with worldwide publishing and direct marketing consulting firms in the D.C.
area. SQL skills a plus.
Salary range $60-75k.
Refer to Job#MM125-Sconsig and email MS Word attached resume to the attention of
Maura Mandrano
Email:
register online at www.AnalyticRecruiting.com
Sr. Managers, Market Research - Pharmaceuticals - NY
Top NY metro pharmaceutical company seeks Senior Managers with proven capabilities
in strategic and creative thinking, thought leadership, quantitative and qualitative
analysis, and problem solving, as well as the ability to lead by example and effectively
design and implement marketing research plans. Market research, managed care, consulting
and/or pharmaceutical marketing industry expertise required. Fluency with secondary
data sources -- IMS, Scott Levin, NDC, etc. -- a major plus. Significant quantitative
and qualitative primary research experience; a keen understanding of customers and their
needs as well as the U.S. healthcare market; and high energy level are essential.
MS/Phd Social Sciences or the equivalent preferred; SAS/SPSS strongly preferred.
Must be authorized to work permanently in the US.
Salary range $85-110k
Refer to Job#MM126 and email MS Word attached resume to
Maura Mandrano
Email:
register online at www.AnalyticRecruiting.com
Scored Underwriting Policy Manager - NY
Major NY financial services firm seeks Manager to develop and implement new policies and
procedure for all scored underwriting decisions.
Responsibilities include:
Re-development of all line assignment policies.
Score cutoff and criteria overlay analysis.
Performance analysis of all underwriting decision by product, vintage, program and channel.
Identification of loss control and growth opportunities across all underwriting channel
Analytic and policy support for Six Sigma initiatives.
Translate policy recommendations into rapid Credit Decision Engine change.
Development of all Fraud Prevention policies within underwriting.
Analysis of new underwriting tools and support development of next generation tools.
QA monitoring of underwriting processes (data & decisioning).
Performance/policy/QA monitoring across multiple sites underwriting process.
Cross RMM policy optimization within product cross-sells.
Special analysis (overrides, marketplace, programs, channels).
Requires:
5+ years Credit Risk Management experience
Advanced SAS skills
Statistical Credit skills
Partnership/Cross Functional teamwork
Hands-on approach / action-oriented
Management experience
Position entails light travel. Superior presentation/communication skills are a must.
Salary to $120k.
Refer to Job#RR236-Sconsig and email MS Word attached resume to
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
SAS position available in MD---must have strong Unix scripting exp.!!
SAS programmer/analyst w/ Unix Shell Scripts
The statistical programmer/analyst designs, writes, and unit tests
Unix shell scripts and SAS programs, statistical -tabulation software,
performs occasional software-configuration and system tasks, writes
documentation and user guides, and provides front-line technical support
for the shell scripts and SAS programs.
Must have heavy Unix Shell Scripting experience!!!!!!
Person should be self motivated, innovative, and posses good
communications and writing skills, and be able to deal directly with
colleagues and operational staff in an unsupervised manner.
To submit your resume in confidence please send a MS Word attachment
to
Email:
and reference job code MDsas
The Consortium, Inc.
www.consortiuminc.com
Analytic Services Executive - Paramus, NJ
Full-Time Regular
Requisition Number: 252
Objectives:
To manage the delivery of analytical product and services to the client
business and to maximize the value of the relationship.
Accountabilities:
Identify business need and apply appropriate analytical tools to solve
that need. Manage customer expectations and ensure customer satisfaction
with company. Lead, motivate and inspire associates. Be a role model in
effectively managing internal company processes by developing a rapport
with key resources.
Description: See required skills, objectives and accountabilities.
Required Skills:
BA/BS in Statistics, Economics or other quantitative field, MS preferred;
SAS and Unix skills;
strong oral and written communication skills;
knowledge of consumer panel and scanner-based;
CPG experience a plus.
Required Experience: 3 years
Required Education: Bachelors Degree
Travel Required: No
Travel Percentage: 0%
Relocation Available: Not Indicated
For consideration, please email your resume to:
Tom Hull
Partner
mangieri/solutions
1 Riverside Road
Sandy Hook, CT 06482
(203) 270-4800 x101
Email:
Web: www.mangierisolutions.com
Trilogy Information Technology will be changing its name to Thinknicity.
Trilogy I.T. is not, nor has it ever been affiliated with Trilogy Consulting
of San Mateo. 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
Regional Clinical Research Associate for the Greater Mid West area
Order C10214
** We have various contract positions that will require travel in order to cover the Greater Mid Western area **
** We are seeking candidates who are local to the areas listed above **
** Relocation expenses are not available for this position **
** 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 **
** We are not in a position to accommodate a visa transfer or sponsorship **
** This position will not accommodate third party or agency representation **
Job Description:
This position is responsible for implementing and monitoring clinical research trials, tracking study progress, and ensuring data integrity.
Review study site regulatory binders for any deficiencies.
Maintain responsibility for drug accountability at sites being monitored.
Ensure that study products are logged, stored, shipped, dispensed, and returned according to ILEX guidelines and FDA regulations.
Design, edit, and review Case Report Forms.
Conduct protocol design and review.
Monitor clinical sites in accordance with GCP/ICH guidelines.
Conduct and coordinate pre-study, initiation, site monitoring, and site closeout visits.
Oversee and coordinate junior level CRA activities.
Edit and review site-monitoring reports.
Candidate requirements:
Must have one-year experience as a CRA in a pharmaceutical, biotech or CRO environment.
Must possess a Bachelor of Science degree from a four-year college or university.
Must have 2-3 years clinical trials monitoring experience in the pharmaceutical industry.
Necessary skills include report writing, MS Office, and verbal and written communication skills.
You will need to be able to travel up to 80% of the time.
Experience in oncology therapeutic area is a plus.
Must possess outstanding communication, organizational, and project management skills.
Contract Length: 6 months
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Bio-statistician II or Senior Bio-statistician
Fulltime position is in South San Francisco, CA
Job F1413
** Fulltime position is in South San Francisco, CA **
** 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:
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
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 U
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Clinical Research Associate
Position is in South San Francisco, CA
Job F1424
** Position is in South San Francisco, CA **
** 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:
The primary focus of a Senior CTM in an Oncology Study is to independently coordinate and supervise all aspects of implementation of a clinical project.
This may include multiple oncology studies and the supervision of Clinical Trial Managers (CTMs), Clinical Trial Coordinators (CTCs) and Contract Research Organizations.
This position works closely with the Medical Monitor for scientific/medical support of the study.
Candidate Requirements
RN/BS degree in the biological sciences or related field or equivalent combination of education and experience.
4+ yrs direct CRA experience preferably in the therapeutic area of oncology, infectious disease or immunology.
Three years directly related experience in the health care industry.
Strong interpersonal communication, problem solving and leadership skills are required.
Travel also required
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Senior Statistical Analyst with at least 3 years of Clinical SAS programming
Position is in South San Francisco, CA
Job F1420
** 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:
As a member of a clinical project team, the Senior Statistical Analyst plans, designs, develops, implements, and maintains software for the monitoring, reporting, and analysis of clinical trials.
The Senior Analyst provides some leadership on technical or work projects.
Develop and execute software to monitor ongoing studies, produce data listings, summary tables and graphics for interim and final analyses and publications.
Create statistical files for bio-statistical analysis. Integrate data across studies within a project.
Provide consistency across protocols within a project on CRFs, database design, analysis files, and tables, listings, and graphs.
Test, document, review and validate all programs according to department guidelines.
Review the CRF design, data management plans, and statistical analysis plans for impact on software systems and study analyses.
Provide consulting and systems support for applications software.
Assist in the maintenance of applications software by identifying enhancements and/or new features with the software developer.
Develop specifications and code for new standardized clinical software tools to help facilitate performing maintenance, analysis, and reporting of clinical data, as needed.
Provide data in SAS transport files, and other appropriate deliverables and documentation for regulatory submissions or for external customers.
Prepare effective communication.
Coordinate data transfer and/or programming standards with CROs and vendors. Work with minimal supervision.
Responsible for broadly defined goals.
May take leadership role on a project team.
May train or mentor others.
Candidate Requirements
A minimum of 3 years of Clinical SAS programming with a BS in statistics, math, computer science, or equivalent experience, or 2 years with an MS in a related field.
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 use of graphics software e.g., SAS/Graph, S-Plus. Understanding of programming standards and accepted software development techniques.
Knowledge and familiarity with data base theory, specifically relational database concepts and ORACLE CLINICAL.
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 teams.
A working knowledge of basic statistics for communicating effectively with bio-statisticians.
Demonstrated competence in data warehouse design and implementation, and integrated database design.
Understanding of regulatory guidelines that affect statistical deliverables.
Experience using SAS to process, report, and analyze clinical trial data.
Thorough understanding of the drug approval process.
Experience interacting with others for defining and implementing user defined reports.
Experience 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 a regulatory filing would be a plus. Experience with UNIX, or similar, operating system.
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Bio-Statistician
Position is in South San Francisco, CA
Job F1412
** 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
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
SAS Software Developer on the Mainframe (MVS)
Fulltime position is in Central Coast, CA
Job F1366
** 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:
Within the Customer Information Management Department you will develop, maintain, and employ information systems to support the strategic and tactical information needs of our client.
You will be responsible for capturing, organizing and integrating data, and staging that data for use throughout the organization.
You will be responsible for developing SAS code to create information deliverables for analysis and decision support.
Other responsibilities include working with the Marketing Managers and Risk Managers to develop business requirements and then executing according to those specifications.
Candidate requirements:
3 to 4 years work experience with Information Systems.
5 to 7 years SAS programming in a Mainframe environment, specifically (MVS) Candidates with Easytrieve will make the perfect candidate.
Experience with Oracle would be a plus.
Must have solid understanding of Business issues.
Education requirement:
A Bachelors degree in computer science/MIS
Otherwise, experience in a related field with a Minor in Business would be acceptable.
SAS Software Developer with Clinical Trials experience
Position is in Sunnyvale, CA
Job C10134
** 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
** We are not in a position to accommodate a visa transfer or sponsorship **
** This position will not accommodate third party or agency representation **
Job Description:
You will be expected to program and document timely and quality clinical listings and summaries for inclusion in worldwide health registration and NDA submissions.
You will respond to ad-hoc requests to produce reports for customers including Clinical, Bio-statistics, Medical Communication and Data Management. You will be responsible for the design and deve
You will coordinate the efforts for a clinical program and provide oversight to the assigned contractors and/or Clinical Programmers.
Candidate requirements:
You must possess 4 years experience with SAS
You must possess a minimum of 2 years experience within a clinical trial environment.
You must have knowledge of Clinical Development, possess the ability to establish and maintain good working relations across functional areas, along with the desire and ability to learn new proces
Contract Length:
6 to 12 months with the possibility of contract-to-hire
Start date Mid December
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Clinical SAS Software Developer
Fulltime position is in Emeryville, CA
Job F1441
** 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 **
Candidate Requirements
Must have two to three years experience programming in a clinical trials environment is the ideal.
Would consider a strong candidate with clinical data programming experience.
Must have at least a BS in Stat or Math or something related.
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Manager--Medical Affairs Clinical Data Management
Position is in South San Francisco, CA
Job F1470
** With our need to conduct face-to-face interviews before presenting resumes to our client, we are able to 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:
You will be responsible for managing a team of Clinical Data Coordinators supporting clinical and commercial projects.
Work collaboratively with Management teams to ensure appropriate data management resource allocation and efficient operations for all therapeutic unit programs
Responsibilities include supervising, training and hiring staff, developing group goals and providing continuous coaching and evaluation of staff.
Key participant on the departmental management team in leading/supporting the data management systems and related processes and standards, while evaluating and implementing improvements as appropr
Requirements
Requires a B.A./ B.S. degree in Life Science or equivalent.
6 years working experience in Clinical Data Management including managing people.
Experience with relational database design.
Knowledge of FDA regulations and familiarity with Oracle Clinical (or similar systems).
Be able to demonstrate excellent communication, problem solving and people/project leadership skills.
Clinical Data Manager with 3-4 years Clinical Data Management experience within a Pharmaceutical company specifically.
Position is in ************************, CA (Bay-Area)
Job F1458
** 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:
Perform timely and detailed data consistency checks on data (both paper data collection forms and on electronic records.
Report and resolve data discrepancies and inconsistencies.
Design and draft paper data collection forms appropriate for various study designs.
Document receipt of completed paper data collection forms from study sites and tracks submitted data clarification requests.
Provide technical expertise as part of a multi-disciplinary data management and analysis team.
Type hand-written technical data into computer database.
Responsible for tracking and quality control of data entry from all sources (paper and electronic).
Coordinate with Quality Assurance personnel to validate data and database tables.
Communicate with project team members and clinical monitors.
Perform other duties as required.
Candidate Requirements
You MUST have 3-4 years of Clinical Data Management experience and it MUST be from within a Pharmaceutical Company.
You need to have an understanding of relational database structures, preferably related to clinical data management.
Ability to design and select appropriate database structures (e.g. table relationships and indexes).
Ability to interact well with multi-disciplinary staff and clients.
Ability to work independently and as a team member.
Ability to meet timelines under pressure.
Ability to manage multiple tasks.
Ability to work under standard operating procedures and Guidelines for Good Clinical Practices
Education Requirement:
Minimum of a Master's or Bachelor's degree in Statistics, Computer Science or related field, or equivalent combination of education and work-related experience.
Type(s) of Computer Science fields :
- Database management.
- Visual Basic.
- Visual Basic for Applications, C+ or other object-oriented computer programming language.
- Knowledge of Microsoft Access and other software for personal computers (e.g. Microsoft Word and Excel).
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Senior Clinical Trials Manager
Position is in South San Francisco, CA
Job F1417
** 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:
The primary focus of the Senior CRA manager is to independently coordinate and supervise all aspects of implementation of a clinical study.
This may include multiple projects, multi-center oncology studies and the supervision of CRAs, CR assistants and Contract Research Organizations.
This position works closely with the Medical Monitor for scientific and medical support of the study.
Candidate Requirements
RN/BS degree in the biological sciences or related field or equivalent combination of education and experience.
5 + years direct CRA experience is required, preferably in the therapeutic area of oncology, infectious disease or immunology.
Three years directly related experience in the health care industry.
Strong interpersonal communication, problem solving and leadership skills are required.
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Clinical Research Associate Manager, with 5 years experience in the related field of the CRA and 3 years Management experience.
Position is in South San Francisco, CA
Job F1446
** 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:
You will be accountable for the functional management of the CRAs and Operations Coordinators for a Therapeutic Unit (TU).
You will be responsible for managing the effective and consistent use of CRA and Operations Coordinator resources on TU program teams.
You will develop CRA and Operations Coordinator resource strategies for support of TU program teams.
You will be accountable for identifying CRA and Operations Coordinator training needs within the TU.
You will be accountable for effective and efficient use of internal and external resources to achieve deliverables.
You will need to identify operational processes requiring improvement, recommend changes, and develop implementation plans.
You will be responsible for effective management of CRA staff (in-house and regionally located, as well as, contractors) and Operations Coordinators in TU, typically 10-15 direct reports.
You will need to ensure personal development plans and succession planning for CRA and Operations Coordinator staff in the TU.
You will be accountable for mentoring direct reports, TU staff, colleagues, and other managers within the TU.
You will be responsible for performance reviews, professional development plans, and vacation management.
You will need to facilitate conflict resolution.
You may need to travel as required to carry out responsibilities.
You will need to effectively allocate budgets related to CRA and Operations Coordinator staffing costs.
You will me a member of the TU management team working effectively to ensure efficient resource allocation to corporate priorities.
You will partner with other Therapeutic Unit and BARDs management to ensure consistency, efficiency and shared learning across TUs.
You will partner with TU management to ensure consistency, efficiency and shared learning across the TU.
Candidate Requirements
BS/BA in Life Science related discipline.
Advanced skills/knowledge in the following areas:
- Ability to think and plan strategically.
- Ability to communicate effectively at all levels.
- Demonstrated resource allocation management skills including risk assessment.
- 5years related Industry experience
- 3years direct Management experience
- Past CRA experience is required
- Experience managing at least 6 direct reports
- Demonstrated growth and development & training of CRA's
- Demonstrated leadership
- Willing to travel a minimum of 30%.
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
Computer Validation Specialist
Contract position is in South San Francisco, CA
Order C10213
Length of Contract: 6 months
** Currently, relocation expenses are not available for this position **
** Currently, visa transfers/visa sponsorship is not available for this position **
** 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 **
** This position will not accommodate third party or agency representation **
Job Description:
You will be dedicated 100% to the documentation testing and verification of the client’s
study management systems along with any related and integration points
You will be dedicated to the documentation, testing, and verification of these study management systems.
You will interface with existing team members (including development and other staff) to achieve the above.
You will be responsible for developing validation protocols (IQ/OP/PQ) in support of Medical
Affairs computerized information systems.
You will work closely with the Validation PM and Project manager to successfully implement
validation plans with protocols
Candidate requirements:
Minimum Requirement is a Bachelor Degree in Computer Science or a related discipline with
approximately two years validation experience.
You must have a good understanding of the principles of software validation in a regulated
industry is required which would include industry guidelines
The job requires experience in the validation of Computerized Information Systems used in
FDA regulated industry (e.g. Study management Systems such as IMPACT, or other enterprise systems SAP, MRP, EDMS).
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word
CIS Validation Specialist - South San Francisco, CA
Order F1415
** 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:
The job requires experience in the validation of Computerized Information Systems
(CIS) used clinical trials (e.g., Clinical Data Management, Adverse Event Reporting, and Enterprise
Study Management Systems).
The successful candidate will be responsible for developing validation strategy (plans)
and testing protocols (IQ/OP/PQ) in support of Medical Affairs Computerized information systems.
Candidate Requirements
Minimum requirement is a Bachelors degree in Computer Science or a related discipline, two
to four year commercial validation experiences, in a GxP environment.
A good understanding of the principles of software validation in a regulated industry is required,
to include, industry guidelines (PDA 18, GAMP, ACDM), related FDA guidelines and regulations
(Part 11, 312, 50), ICH GCPs.
Good interpersonal and written communication skills are highly desirable.
Please quote the job order reference when you are responding.
Please attach your resume when responding, preferably in Word.
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
Health Data Analyst Opening - Portland, ME
Health Dialog has an immediate opening for a full time, experienced
Research Data Analyst in our Portland, Maine office.
Health Dialog uses a variety of methods and resources to assist clients in
managing their chronic disease populations. These include services for
identifying and describing the population, risk modeling, gap analysis,
developing patient registries, outreach, education and support, and impact
assessment. The successful candidate will have experience managing and
analyzing large volumes of health care claims data, using various
statistical methodologies. Experience using SAS, a common relational
database management system, SQL and a Masters or higher level education in
biostatistics or epidemiology are preferred. Good oral and written
communication skills, as well as some knowledge of pharmacy claims are also
desirable.
Contact:
Charlotte Phillips
Health Dialog Data Service
23 Spring Street, Suite C
Scarborough, ME 04074
tel: (207) 396-5324, fax: (207) 396-5348
Email:
Email:
SF Bay Area: Biostatistician/Data Analyst, Eos Biotechnology
Biostatistician/Data Analyst
South San Francisco, CA
Eos Biotechnology, Inc. is a progressive, privately financed biotech
company focused on developing and applying genomics-based technologies for
the discovery of new therapeutics. We currently have an excellent
opportunity in our South San Francisco facility for Biostatistician/Data
Analyst to join our expanding data analysis team.
You will work in a fast-paced, deadline-driven setting designing and
writing programs that perform sophisticated statistical analyses. You will
research and evaluate existing state-of-the-art methods and algorithms in
statistical learning; you will use these algorithms to devise and implement
data analysis tools that will be used by other researchers; you will
interact with research staff and provide technically and theoretically
sound advice on data analysis and experimental design.
Candidates must have:
PhD or equivalent experience in statistics,
biostatistics, or related quantitative field (Master's degree with very
relevant experience will be considered); 4+ years' programming experience
in data manipulation & complex statistical analyses; Extensive and solid
experience with statistical learning methods; demonstrated ability to
research, evaluate and write programs that implement novel statistical
learning and data analysis algorithms, as well as the ability to
communicate these statistical methods and ideas to scientists in other
fields; a solid understanding of statistical techniques (linear & logistic
regression analysis, analysis of variance, cluster analysis, factor
analysis, etc.); proficiency with Windows 95/98/NT (Excel & Word) and
excellent analytical, organizational and written/verbal communication
skills. Proficiency with SAS and/or work experience in genomics and,
specifically, analysis of gene-expression data is desirable. Knowledge of
data analysis packages such as S-Plus, Mathematica, MATLAB and/or knowledge
of RDBMSs such as MSAccess, SQLServer, MySQL is a plus.
We offer attractive compensation and benefits, including three week
vacations per year, medical, dental, vision, 401k, free parking, free lunch
on Fridays, and generous stock options. Eos fosters an environment that is
friendly and challenging and offers the opportunity to work and grow with
talented people toward achieving common goals.
EOE.
How to Respond:
Please note: Job code 02-04-Eos is required for all communications
regarding this position.
Email:
Via Mail
Eos Biotechnology, Inc.
HR Department
225A Gateway Boulevard
South San Francisco, California 94080
Attn: Job Code 02-04-Eos
Via Fax 650-583-3881
Email:
SAS Analyst Position(s) - Indianapolis, IN
SAS Analyst(s) - Macros, STAT, Clinical Trials - Salary DOE
Looks for SAS Analyst(s) who will work in-house as a team member to develop
a cutting-edge, enterprise-wide I/T toolset for analysis and reporting of
clinical trials data. This includes:
a) writing accurate, well-documented SAS programs based on customer requirements and programming standards, and
b) thorough unit testing.
REQUIRED SKILLS:
SAS - at least 1 year post-academic development experience creating reports, datasets and analyses.
Systems Development - minimum of 1 year of coding, systems testing and documentation experience in an IT role.
Excellent team/interpersonal skills.
Excellent communication skills.
Bachelor's degree.
DESIRED SKILLS:
Familiarity with analysis of clinical trials data or agricultural
research trials data in the pharmaceutical industry or a Contract Research
Organization (CRO).
Working knowledge of eXtensible Markup Language (XML) documents.
Experience with JAVA.
Working knowledge of Object Oriented concepts.
Systems Development - experience gathering customer requirements,
designing and validating systems.
Working knowledge of statistical concepts.
Excellent opportunity to expand SAS skills with XML and Java in a creative
environment.
For more information, contact
Mia Lyst
Email:
Email:
Looking for 3-5 Sr. SAS Contractors with Energy/Trading experience - New Orleans, LA
Our client has an immediate need for Sr. SAS consultants for a 6-month
contract in New Orleans, LA. Consultants will work on new development
for an energy trading project. We are looking for people with deep SAS
skills combined with industry knowledge. (energy/trading/risk mgmt)
Consultants must have SAS experience with 2 or more of the following:
Offer Management
Forecasting
Risk Dimensions
Pricing
Scheduling
Settlements
Portfolio Management/Optimization
* Knowledge of EDI 1.4 txn would be a plus.
For immediate consideration please contact:
Email:
Senior Systems Analyst - NJ
Join this large NJ based pharmaceutical as a Senior Systems Analyst.
Responsibilities will include managing and planning and execution of
individual datawarehousing projects. Translating business and team
requirements into data warehouse solutions (40%). Design, build and
validate clinical compound and overall data warehouses (25%). Support the
implementation of clinical data warehouses (eg., create data marts, surface
the data in other applications, etc.) (10%). Investigate up to date on
technology/software: assess potential impact and potential value of new
tools, implement as appropriate (10%). Provide training and demonstrations
(10%). Participate in the continuing process integration efforts (5%).
Candidates must have 6-10 years experience in clinical research/biometrics
environment. Also must have at least 3-4 years of SAS experience. Good
communication and negotiation skills and a BA or BS degree preferred.
The Cambridge Group was established in 1976 and has grown to be one of the
largest recruiting firms with a nationwide client base. Our Pharmaceutical
Division specializes in the placement of clinical information systems,
programming, and data management professionals in research and development
settings.
For more information on these and other opportunities please follow the
contact information listed below. Information provided to us will be held
in strict confidence. Your credentials will not be presented for any
opportunity without your specific permission. Thank you for your
consideration.
Kim York or Traci Palmer
phone (800) 525-3396
Email:
Email:
web www.cambridgegroup.com/pharm.html
REPORTING, ANALYTICS, AND DATA WAREHOUSING ANALYST/PROGRAMMER
FULL-TIME PERMANENT CA CENTRAL VALLEY
Salary range: $3,857 to $7,896 per mo
F/T pos avail on or after 5/1/02 in the Office of Institutional Research,
Planning, and Accountability. B.S. in an Sociology, Psychology, Political
Science or analytical science; masters preferred. Minimum 5 yrs of
progressively responsible administrative or professional experience that
demonstrates ability to conduct complex analyses of problems in assessment,
planning, institutional research or decision support office required. 3 yrs
or more of programming experience in SAS (data mgt, survey design and
analysis) preferred. Open until filled. Application screening to begin on
or after 4/5/02.
Application and complete job announcement available at
www.csustan.edu/hr or at the
Human Resources Office
California State University
Stanislaus
801 W. Monte Vista Ave.
Turlock, CA 95382
PH 667-3354. EOE/AA
Thomas Kunselman
Manager, Data Warehousing & Analytics
Institutional Research, Planning, and Accountability
California State University, Stanislaus
801 W. Monte Vista Avenue
Turlock, CA 95382
Voice: (209) 667-3647
Fax: (209) 667-3251
Email:
Unit 9 Representative, CSEA Union Local 1000 Chapter 308
Full-Time SAS expert at L. L. Bean, Inc. - Freeport, ME
L. L. Bean, Inc., the direct marketing retailer of outdoor apparel and
equipment, has an immediate opening for a Full-Time SAS expert, with SQL
experience and familiarity with statistics and marketing.
Main Function:
You will hold a key position in the Corporate Marketing Department,
responsible for the management of all customer data used in the
segmentation and database research area. Responsibilities include:
Developing sophisticated research files.
Serving as liasion to internal I.T. and external data vendors.
Managing the Analytic & Data Infrastructure aspect of Customer
Relationship Management.
Providing specialized programming support.
Formulating ideas and action plans to enhance/augment customer data.
Taking a proactive approach to understanding data sources, data
requirements, efficient data access techniques and statistical modeling.
Qualifications:
3-5 years programming experience. Fluent in SAS and/or SQL.
Knowledge of database marketing, DB2, server and SP technology.
Proven project management skills.
Specific Qualifications:
Extensive and intensive experience using SAS to access data in a variety of
stores, including flat files and relational databases, on a variety of
platforms including MVS, AIX Unix, and Windows.
Fluent in SQL, preferably DB2's implementation, including common table
expressions, global temporary tables, and intepretation of EXPLAINs.
Comfortable with manipulating high volume datasets. Understanding of code
efficiency techniques for conserving CPU, space and/or manpower.
Proactive in matching available technology with information needs of
department. Ability to learn new software and use as appropriate.
Understanding of data sources and analytical techniques, and what
conclusions they do or do not support.
Understanding of the data needs of statistical modeling efforts.
Ability to exchange information with technical support staff and understand
the implications of technical communications for Marketing management.
This is a full-time, on-site position. U.S. resident or valid green card
required. For more information or to apply, please contact
Peter Liberatore
Manager of Segmentation and Database Research
L. L. Bean, Inc.
Casco Street
Freeport, ME 04033
Email:
Email: