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Manager, Statistical Programming
Top five global pharmaceutical on East Coast is searching for qualified
candidates to manage SAS programming activities involved in the processing,
analysis and reporting of clinical trial data. Other responsibilities
include playing a leadership role in projects that investigate new
technologies and collaborating in the development of standard data models
and reports. Qualified candidates must be permanent residents of the US
and have at least 8-10 years of experience programming clinical trial
data. Excellent oral and written communication skills are required.
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
fax (203) 226-3856
Email:
SAS Opportunity - Business Process Analyst, B/W Analytics - Lancaster, PA
For immediate consideration via a CONFIDENTIAL on-line interview, please
click below. This is the preferred method of response.
Click here to apply
Performs analysis of routine to moderate complexity in support of the ABP business
planning cycle. This individual accesses, manipulates, and analyzes data to determine
causal factors, relationship, and opportunities for improvement/achievement of objectives.
Areas of focus include:
commercial and retail sales/marketing adhoc requests, commercial pricing reporting,
consumer demographics, sales promotion effectiveness, and market share performance.
Person is also responsible for continued daily & monthly maintenance of group internal
data structures and programming interfaces.
Person will also be responsible for user support and training of sales portion of SAP
BW and Cognos information cubes/reports.
Click here to
apply
Education: Preferred undergraduate and graduate degrees in the areas of Operations
Research, Statistics, or Quantitative Business Analysis. A strongly mathematically
oriented MBA may also be considered.
Required programming skills: SAS
We prefer a candidate to have solid programming skills in SQL, SAP BW, Visual Basic.
Required software skills:
Microsoft Office, Windows 2000/NT, Microsoft Access (at the power user level), Cognos
Suite, MapInfo, Sybase, and Oracle.
Familiarity with Oracle Sales Analyzer and Spectra Enlighten is considered a plus.
Ability to master internal reporting systems: HEAT, Price Is Right, Spectra,
F.W. Dodge Analytical products (Market Analyzer, Dataline, Market Leader), Sales
Analyzer, SAP BW, and Enlighten.
Experience with consumer demographics modeling, mapping, and direct marketing models
is preferred.
Click here to
apply
This position is unique. And, if you have the skills to be successful in this position,
you are unique too. We are willing to consider a telecommuter for this position -- so
don't let geography stop you from letting us know more about you!
Click here to
apply
Armstrong World Industries, Inc. is a manufacturer and marketer of interior furnishings,
most notably vinyl and hardwood floor coverings, acoustical ceilings and suspension systems.
With sales in excess of $3.0 billion and over 15,000 employees, Armstrong is a recognized
leader around the world. To learn more about us, visit our Home Page:
http://www.armstrong.com. We are an equal opportunity employer that is committed to
a diverse workforce through affirmative action.
Click here to apply
Armstrong World Industries
c/o HRWebXpress.com, LLC
831 DeKalb Pike
Blue Bell, PA 19422
Web: http://www.armstrong.com
Our clients has retained Open Source Technology, Inc for a SAS programming and development project in
New Jersey. The firm is a multi-billion dollar drug manufacturer in the Pharmaceutical industry.
The consultant will be performing SAS programming for processing clinical trials data to produce data
listings, summary tables, statistical analyses and graphics for regulatory submission, publication and
promotional material. People need two to four years minimum experience in statistical programming for
pharmaceutical clinical trials.
Job requirements:
Base/SAS SAS/STAT Macros
Biology
Working side by side with a Statistician
Pharmaceutical background- clinical trials ( strongly desired )
Knowledge of FDA requirements for data management systems and system validation.
Excellent written, verbal, and organizational skills.
Our client is a leading Biotech firm. They are looking for a lead statistical programmer. They may consider
contract professionals with a willingness to consider permanent employment.
The main responsibilities are to develop, validate and maintain general-purpose and ad hoc SAS programs
for the validation, manipulation, analysis and reporting of clinical, pre-clinical, and post-marketing data. To
provide a specialized area of expertise in statistical programming, e.g. software and systems analysis and
development; e-submission techniques and processes; non-SAS based presentation and reporting techniques;
data warehousing. To provide guidance to other SAS programmers, statisticians and other personnel in this area
of expertise.BS in computer science with course-work in data structures and mathematical / statistical programming.
Minimum of 5 years experience in reporting and analyzing clinical data in SAS in a pharmaceutical or
biotechnology or CRO setting.
Please contact :
Louis LaMattina
Email:
Senior Statistical Programmer Job Posting - Cambridge, MA
No Recruiters Please
We have an opening for a Senior Statistical Programmer Vertex
Pharmaceuticals
About Vertex
Founded in Cambridge, MA in 1989, Vertex Pharmaceuticals Incorporated discovers,
develops and markets small molecule drugs that address major unmet medical needs.
We have eleven drug candidates in development to treat viral diseases, inflammation,
cancer, autoimmune diseases and neurological disorders.
About the position (Job code 710-5)
The ideal individual will be very experienced developing and validating SAS code and
applications to solve problems which meet project and department needs, primarily the
presentation and analysis of data collected in clinical trials.
Interact directly with Biostatisticians, Clinical Data Mangers, Statistical Programmers,
Clinical Development staff, IS, and management as the leader and technical advisor of a
programming team. Direct and coordinate activities of programmers assigned to a project.
Perform quality assurance checks of code and outputs. Construct estimates of project
programming resource requirements, timelines, and routinely brief management on team
accomplishments, status, and issues.
Apply your expert skills in writing SAS code to produce listings, tables, and figures
and to develop GUI applications. Make technical presentations on topics relevant to
your area of technical expertise including SAS training.
Utilize your substantive knowledge of medical data, the design and phases of clinical
trials, statistics, relevant FDA regulations, and the pharmaceutical and biotechnology
industries to the implementation of tasks.
You will work independently under general supervision.
Minimum requirements
B.S. in Computer Science, Statistics, or a related field, and 7 to 10 years relevant
experience.
M.S. in Computer Science, Statistics, or a related field, and 5 to 8 years relevant
experience.
Note: Relevant experience is SAS programmer/analyst experience in the conduct of clinical
trials for regulatory submissions to the FDA or European authorities.
To find out more information
http://www.vpharm.com/jobs_detail.php3?tid=1&job_id=565
To apply
You may apply for this position in one of the following ways:
Submit your resume directly via the web (preferred method)
http://www.vpharm.com/submitResume.php3?tid=1&cid=4&Position=Sr.+Statistical+Programmer%2C+710-5
Mail to:
Recruiting - Dept. W
Vertex Pharmaceuticals Incorporated
130 Waverly Street
Cambridge, MA 02139
Fax: +1 617 444 6645
If you mail or fax your resume, please specify the position in which you are interested.
Vertex Pharmaceuticals Inc., is an EQUAL OPPORTUNITY EMPLOYER.
Email:
SW Jules, Inc.
Ms. Julie Youmans-Smith
8760-A Research Blvd., Ste 264
Austin, TX 78758
Phone: 501-723-8492
Fax: 501-723-5136
Email:
Web Site: www.swjules.com
SW Jules, Inc. is a High Tech, Pharmaceutical and
Managerial recruiting and consulting firm. Please submit your resume for
this position by either faxing or attaching in e-mail. We do not forward
resumes until we get your permission to do so. ALL RESUMES RECEIVED ARE HELD
AS CONFIDENTIAL.
Director Biostatistics for Major Biotech Company in California
SUMMARY:
Candidate for this position will have strong Biostatistics experience
working on Phase I-IV pharmaceutical research studies within a Biotech firm
or Contract Research Organization. Will supervise data analysts and statisticians.
Involved in the design, implementation, and analysis of clinical trials and other product studies.
Responsible for planning and directing the statistical analysis of data from studies, and of
assuring the quality and accuracy of statistical sections of study protocols and clinical reports.
Participate in conference calls/meetings with regulatory agencies
and prepare responses to regulatory agency questions regarding statistical
aspects of clinical trial and other study design and analysis.
Closely involved in the preparation of clinical and other
statistically oriented reports in support of product licensure as well as
new indications and license amendments for previously licensed products.
Responsibilities also include the supervision and development of data analysts and statisticians.
Qualifications and requirements:
Ph.D. in Statistics, Biostatistics
8+ years experience in Statistical analysis with minimum 5 years in biotech setting
Strong management and supervisory skills.
Director Biostatistics(Texas)
If you are someone who enjoys building an office for a well established CRO
look no further. The challenges and rewards are here.
SUMMARY:
Candidate for this position will have strong Bio-statistics experience
working on Phase I-IV pharmaceutical research studies within a Biotech firm
or Contract Research Organization. Will manage the bio-statistical group and
supervise data SAS programmers and bio-statisticians.
Involved in the design, implementation, and analysis of clinical trials and other product studies.
Responsible for planning and directing the statistical analysis of
data from studies, and of assuring the quality and accuracy of statistical
sections of study protocols and clinical reports.
Participate in conference calls/meetings with regulatory agencies
and prepare responses to regulatory agency questions regarding statistical
aspects of clinical trial and other study design and analysis.
Strong writing skills. Statistical plans, protocols and client communication.
Strong marketing and communication skills.
Individual will be highly visible and involved in business development.
Minimum Qualifications:
Ph.D. in Statistics, Biostatistics, Epidemiology or Math and 5+ years in a biotech or CRO.
Associate Directors with 5+ years experience or SR BIOSTATISTICIANS with 7+ years experience
will be considered. If you are looking to move up here is your chance.
Strong SAS experience.
Strong management and supervisory skills.
Contact:
SW Jules, Inc.
Ms. Julie Youmans-Smith
8760-A Research Blvd., Ste 264
Austin, TX 78758
Phone: 501-723-8492
Fax: 501-723-5136
Email:
Web Site: www.swjules.com
Sr. Manager Database Services - Plainsboro, NJ.
Company Information
At Bristol-Myers Squibb, our mission is to extend and enhance
human life by providing the highest quality healthcare products
and services. Our medicines are making a difference in the lives
of millions of customers across the globe. Recently, Bristol-Myers
Squibb was named America's Most Admired Pharmaceutical
Company by FORTUNE magazine.
Primary Responsibilities
Develop strategy for data mining and database analysis for customer needs.
Build and run queries using SAS and OLAP.
Collabarate with Market Research, brands, & agencies to establish metrics for marketing initiatives.
Use EDA & statistical methods to develop statistical models.
Perform detailed end of campaign analysis.
Job Qualifications
MS or higher in Statistics or Economics. 5+ years in database marketing.
Prior experience with SAS, OLAP tools such as Epiphany & Business Objects.
Knowledge of EDA, CART & CHAID Decision Trees.
Strong experience with MS-Access, MS-Excel, MS-Powerpoint, SQL and Oracle.
Understanding of consumer and healthcare marketing principles.
For Additional Information
At Bristol-Myers Squibb, we're committed to providing our employees with career and professional development
opportunities, highly competitive compensation and benefits, a diverse and challenging work environment and a focus on
work/life balance.
Please email your resume to
Elaina Hoffman
Email:
We are an equal opportunity employer by choice.
12 East 41st Street, 9th Floor
New York, NY 10017
Phone: 212 545-8511
Fax: 212-545-8520
Website: www.analyticrecruiting.com
Senior Marketing Database Statistician - Chicago
Suburban Chicago consumer products company seeks DB Marketing Statistician
to develop statistical and economic based models and perform ad-hoc analyses
to drive fact based decision making leading to profitable customer growth
for the enterprise.
Responsibilities:
Perform backend mailer analyses
Consult with CRM and business partners on analytic methodologies direct to
customer analyses and explain results in a clear precise manner.
Requires:
2+ years experience working as a statistician in a retail, direct response
or CRM environment.
Strong presentation and written skills.
Experienced in the analysis of mainframe-based databases, especially SAS.
SAS or SPSS in a client-server environment is also desirable, as is an
understanding of SQL.
Project Management skills a plus.
Salary to $75k + Bonus.
Refer to Job#RR230 and email MS Word attached resume to the attention of
Rita Raz
Email:
register online at www.AnalyticRecruiting.com
Senior Consultant, Database Marketing - Washington DC area
Database marketing consultancy seeks experienced direct mail professionals to manage the definition, development
and delivery of business intelligence and analytical projects for their clients. Successful candidates must have at
least four years experience in database marketing with heavy emphasis on direct mail and strong quantitative skills.
SAS, OLAP, relational database experience strongly preferred.
Salary to $110K.
Refer to Job#MM121-SConsig and email MS Word attached resume to the attention of
Maura Mandrano
Email:
register online at www.analyticrecruiting.com for position# mm121
Contact:
Analytic Recruiting
12 East 41st Street, 9th Floor
New York, NY 10017
Phone: 212 545-8511
Fax: 212-545-8520
Website: www.analyticrecruiting.com
SAS/Stat. Positions in the Pharmaceutical Industries
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 Permanent Resident or Citizen of the U.S., or Canada, and are
interested in opportunities in New York, New Jersey, Connecticut and
Pennsylvania , then please contact me. The jobs below are for NY, NJ and CT.
Sincerely,
Barry Rosen
Global Search Recruitment Systems, Inc.
Phone: 1-800-652-5122x301
Fax: 973-781-1999
Email:
www.gsearch.com
Major Pharmaceutical Corporation:
Statistical/SAS Programmer Analyst, NY and NJ.
Salary Range Low 60600 - Salary Range High 96800
Job Description:
Provides statisticial programming support and validation of
analysis datasets, pooled datasets, statistical tables, summaries, figures and listings for Phase II-III clinical trials, and the integrated Safety Summary. Employs standardized programs where appli
Detail Info
Employment Type Full Time
Experience 4 years
Education Bachelors Degree
Travel Percentage 0
Relocation
Minimum Requirements BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences or related field(s). Intermediate SAS programming skills, with 2-5 years experience i
interpersonal and organization skills. Attention to detail and correctness. Working knowledge of office tools.
Major Pharmaceutical Corporation
Sr. Biostatistician / Assistant Director, NY and NJ.
Salary Range Low 70600 --Salary Range High 126800
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.
Employment Type Full Time
Experience 8 years
Education PhD FLSA
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 a
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.
CRO Corporation in CT.
Clinical Data Programmer
Low Range Salary - $50,000 High Range Salary $70,000.
Job Purpose/Summary
Develop and maintain SAS programs in support of the clinical data management
process. Provide SAS based data programming support for final database
preparation, statistical reporting, data transport, and QC review. Provide
program documentation is support of testing and validation requirements.
Core Responsibilities
Data programming: SAS program design, and maintenance in support of the
following functions:
Data edit checking
Data extracts from sponsor or internal database systems
Data mapping and conversion to sponsor data delivery specifications
Data listings in support of data cleaning and study reporting requirements
Patient data profiles in support of the database QC process
Data transports
Assist statistical programming department in preparation of final study report
Program validation:
Documentation of SAS program design, and maintenance
Assist in the development of programming standards and validation procedures
Adherence to sponsor provided or internally developed programming standards and validation procedures
Support activities:
Assist in validating the completeness, accuracy and consistency of the clinical database on an ongoing basis through the use of computer-generated
reports and listings.
Interface with Clinical, Safety, Biostatistics and Data Management personal to resolve problems and issues dealing with clinical data.
Performs other tasks required within CDM as necessary to meet the needs of the business.
Quality Control:
Organizes and maintains written documentation for quality and audit processes.
Maintains all appropriate records and produces program documentation and
validation reports as needed.
Developmental Responsibilities
May participate in the definition, development, and validation of ad hoc
listings and reports for use in the validation of the clinical database.
May participate in the definition, development, and validation of audit
sheets, listings, and/or reports used in the quality control process.
May participate in the review of final data listings, tables and graphs to
facilitate the validation of the clinical database, when required.
May participate in the validation and QC of Annual Safety Tables when
required
May participate in the development and/or maintenance of SOPs, project
books and other project management tools.
May communicate (written and/or verbally) with Sponsors
Qualifications
Candidate/incumbent should have a minimum of 2 years experience in SAS
clinical data programming or 4 years of SAS macro level programming.
Bachelorıs degree in computer science or related field is preferred. Must
be able to work in environment with strict timelines and must be flexible.
Candidate/incumbent should be familiar with using PC and mainframe based SAS
version 6.xx or 8.xx. Candidate/incumbent should be able to work independently and understand and carry out detailed instructions. Good written and verbal skills are also necessary
Growth Opportunities
Senior Clinical Data Programmer
Manager, Clinical Data Management
Tasks, duties, and responsibilities as listed in this job description are
not exhaustive. The company, at its sole discretion and with no prior
notice, may assign other tasks, duties, and job responsibilities. Further,
nothing contained herein should be construed to create an employment
contract. Employment with all of the companyıs employees remains at will
and can be terminated at any time, with or without cause, at the option of
either the employee or the company.
Contact:
Barry Rosen
Global Search Recruitment Systems, Inc.
Phone: 1-800-652-5122x301
Fax: 973-781-1999
Email:
www.gsearch.com
A STAFFING SOLUTIONS COMPANY
Numeric is a staffing solutions company focused on the Pharmaceutical, Market Research and Healthcare industries.
We recruit for contract, contract to permanent, and permanent placement. Numeric offers our contractors a full benefits
package, which includes Medical, Dental, Life and Disability insurance, paid time off, educational allowance, relocation
allowance and 401(k). Numeric handles all work visa needs, and will sponsor for permanent residency after 90 days of
employment.
***We have positions nationwide for Clinical SAS Programmers with all levels of experience!***
The client is a non-healthcare consumer products company. Requirements are statistical expertise in
design of experiments, categorical data analyses, and linear models. Experience with mixed models is
a plus. Preference given to those candidates with an advanced degree in operations research,
mathematics, statistics or engineering. Excellent communications and strong SAS skills are required.
This can be a permanent or long-term contract position.
Seeking Clinical SAS Programmers for positions on the West Coast and in the Mid West.
Responsibilities include reviewing protocol, case report forms (CRFs), and statistical analysis plans
(SAPs) for clinical trials; annotating CRFs; programming edit check specifications for data validation;
generating the derived data sets for the statistical analysis; generating listings and tables for
clinical report in SAS; creating and managing production of analysis files, summary table listings,
and graphs for Clinical Trials and FDA Submissions.
SAS skills must include SAS/GRAPH, SAS/BASE, SAS/MACRO, SAS/STAT. Excellent communication skills are required.
Experience in regulatory environment and FDA submissions is a plus.
Visit our website at www.numericjobs.com or contact us to discuss your specific needs toll free at 888-399-4990.
Peg Boas
Recruitment Manager
Email:
|
Bill Kelly
Manager, Pharmaceutical Services
Email:
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Short Term SAS Contract Opportunity - Columbus, OH
DeskTop Solutions is looking for a short term SAS contractor/consultant to work with one of our clients in the Columbus, OH area.
Our client is in the process of defining some new health care studies with the State of Ohio. The studies involve Narcotics use,
Long Term Care, and use of medications in nursing facilities.
The position is relatively short term (1-2 months) and will work with the client's nurse project manager and be the interface with
the state to help finalize the study details and to work on determining the sample that should be used in the study. The SAS
Consultant will be able to get some direction from our current analysts but the person may have to dig out some facts on their own.
The person would need to reside at our client's location in Columbus.
We will need someone that is knowledgeable in health care data (e.g. claims, HCFA 1500, MDS, etc.) as well as statistics and
study design. Good knowledge of working with SAS is also important.
It is potentially possible that we could allow the person to reside here part of the time and to reside elsewhere at other times. It is
also possible that this could be a part time activity although I can't say that for sure.
This contract has an hourly rate of $65 per hour.
Email:
Email:
Sr. Business Information Analyst - SAS Programmer - Portland, OR
Responsible for providing data management and programming support to the Quantitative Analysis &
Modeling group and the Risk Department. Extract, clean and organize credit bureau data, credit card
application and master file data; write programs, macros, and common code for use in creating complex
datasets. Audit and check files and reports to ensure highest level of quality. Responsible for assessing
computing needs of group and communicate needs to appropriate department to acquire resources;
generate SAS programs of moderate complexity; work independently and with others; identify where
processes need to be created or articulated to resolve programming problems.
Intermediate to advanced SAS programming skills with good working knowledge of SAS BASE and
SAS MACRO required; knowledge of JCL, ISPF and SYNCSORT; 2+ years SAS programming
experience in data management; high-level SAS programming experience in Windows and mainframe
(MVS/TSO)required; BS degree in Computer Science, Math or Business Information Systems desired;
Visual Basic programming experience desired.
Contact
Prasad Ravi
Household Credit Services
Tigard, OR 97223
Fax: 503-686-2836
Email:
SAS Programmer/Analyst job in Los Angeles
I'm a professional recruiter doing a search for a client in Los Angeles looking for an
experienced (at least 6 years) SAS software developer. Candidate must have experience
in using clinical trials data (at least 3-5 years). Please email me for more information
on this job and send your resume as an attached Word document.
Susan Bernstein
Email:
Click Here for Numeric Postings
Data Mining Manager West Coast - Perm
Programmer/Analyst Texas 3 month contract + extensions
Statistical Modeling Analyst West Coast - Perm
SAS programmer (2 Openings)- Delaware - Fulltime
1: Programmer needed to perform complex programming and specialized technical
work using SAS and other programming languages, perform business analysis,
develop programming to meet reporting requirements, and make recommendations
to senior management. The primary focus will be the development of "audit"
programs and reporting to assist process owners in identifying process
failures and opportunities.
2: Programmer Analyst with project management skills needed to initiate and
perform datamining, data acquisition, and business analysis using complex
programming and technical work in SAS and other programming languages. Must
have an excellent working knowledge/ understanding of statistical
applications. May be required to perform programming for account cleanup,
to provide programming to meet reporting requirements, and to provide
concurrent analytical and programming support for multiple project teams.
Must have a good sense of curiosity, and be interested in non-routine
process improvement/problem solving work; proactive type. Must have
excellent written, verbal, and facilitation skills necessary to work well
with others, and to provide sound business recommendations to management.
Contact:
Rachel Pereira
Email:
SR. SAS PROGRAMMER
Director of Healthcare Data and Programming
Los Angeles, CA
Click here to see details of jobs
Contact information:
Randee Fowler
Recruiter
415/381-4051
Email:
Enterprise Data Consultant - Hartford, CT
Click here to read more about this job
James Scanlon
Executive Director, Research & Intelligence
CIGNA Retirement & Investment Services, H10E
280 Trumbull Street, Hartford, CT 06103
ph: 860-534-7092, fx: 860-534-3320
Email:
SAS Programmers - UK
I am seeking SAS programmers for an excellent opportunity in the UK. My
client will pay all relocation costs and sponser work permits:
Minimum Requirements
BA/BSc or equivalent experience in computer science, mathematics,
statistics, or life sciences. Good programming skills with a working
knowledge of SAS in the pharmacutical environment. Good understanding of
clinical trial practices, procedures, methodologies. Excellent verbal and
written communication skills. Continuous improvement mentality and
attention to detail. Working knowledge of office tools
Natalie Fforde
Director
Pharmaceutical Resourcing
Mind Consultancy Ltd
Oakfield House
35 Perrymount Road
Haywards Heath
West Sussex
RH16 3BX
Email:
Tel: +44 (0) 1444 473390
Fax: +44 (0) 1444 417874
Website: www.mind.co.uk
SAS Programmer contract - Edmonton, Alberta, Canada
Click here to see more about job
Contact: Jay
Email:
Web: www.imexsystems.com
imex systems inc.
1590 Matheson Blvd.E Unit # 26
Mississauga ON. Canada L4W 1J1
Clinical SAS Programmer - Wilmington, DE
Reference #: 101449833BFN
What You'll Do:
You will be responsible for writing edit check programs and listings of clinical
trial data in SAS, as well as uploading SAS transport files onto UNIX and NT
systems.
Annotate CRFs and create database design specifications.
Hours of this position are Monday - Friday, 9 am to 5:30 pm.
Your Required Skills:
2 years experience in SAS programming of clinical data on HP/UNIX and Windows NT
platforms.
Solid clinical experience.
Previous experience writing edit check programs against clinical trial data.
Bachelor's Degree in Computer Science or related Health Science.
Contact Info.:
Jeanne, Sunita, or Erica
800-229-5709
Web: www.DevonClinicalStaffing.com
Email:
SAS Jobs - South West of England
I have SAS jobs all over the south west of England, mainly in Oncology research (pharms) and Credit Risk (finance).
SAS programmers - based BERKSHIRE (silicon valley of UK) and south coast of ENGLAND
I have exceptional roles for SAS programmers in the UK. Working in the banking, insurance and pharmaceutical
areas it is essential that you have a minimum of 12mths SAS programming. Ideally base, macro and V8. The roles
will give you career development abd training into new areas. With alot of work being done over the intranet you
will get exposure to web technologies. My clients are well established and successful and look to employ enthusiastic
and focused SAS people. Call today and make that move to change your career for the better
Annette Richardson
Progressive Computer Recruitment
Email:
Email:
Permanent Full Time Pharma Job Opening in Berkeley California
Click here for Xoma posting
Clinical Database Administrator, Job Posting, San Francisco, CA
Click here to see posting
Tom Whiting
Enterprise Resource Group
San Francisco, CA
(voice) (415) 221-6300
Email:
SAS Developer - Hartford, CT
SAS DEVELOPER
Work within a dedicated IT team supporting Specialty Actuarial as a SAS Developer
on our ad hoc team. We are in the process of transitioning our legacy based applications to a
mid-tier utilizing SAS software (V8.2 for Windows, Enterprise Guide, STAT and Graph). The
selected IT professional will utilize their SAS expertise along with their knowledge of our
business to produce state required reporting and miscellaneous ad hoc's. Frequent and effective
communications with our internal and external customers is vital to the success of this position.
This is an exciting opportunity with tremendous visibility and growth potential.
QUALIFICATIONS:
Exceptional SAS development
Problem solving and customer service skills
Minimum 2 years experience, 5+ years preferred
Knowledge of insurance business and The Hartford's main data sources (i.e. CCPS, NPPS) helpful
College degree preferred
Team player who can also work independently is mandatory
If interested, contact
Amy Coates
at (860) 547-8119
Email:
Ims/Cics/Db2 Performance Consultant / Contract - Hartford, CT
Job Description:
Seeking a programmer with excellent skills in IMS/DC , CICS and DB2 Performance.
Requirements include:
DB2 performance experience with SQL performance a plus
IMS/DC performance experience and/ or CICS
SAS language and MXG or MICS
Omegamon monitors for MVS, IMS and DB2, and TMON for CICS
STROBE and APM/Power
Also requires excellent communication skills to be able to work with user community.
This individual needs to have senior level experience with these applications so that
they can actively produce in a very short timeframe.
This is a contract opportunity. All resume submissions must have qualifications
listed above. Corp. to Corp. arrangements are available on a limited basis. Local
candidates will be considered first.
Candidates should email resumes to the listed email address - NO CALLS PLEASE.
All candidates must meet minimum requirements for experience. CSA/Tiger is an
Equal Opportunity Employer.
Email: