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SAS Openings as of September 16, 2002 - California & Texas
DataLogic Consulting Inc.
12966 Euclid St., Suite 450
Garden Grove, CA 92840
Tel: (714) 530-6005 x104
Fax: (714) 530-6129
Web: www.dlgi.com
Email:
Email:
your desired hourly rates and availability.
Questions and/or inquiries should be directed to (714) 530-6005 ext. 104
NOTE: This listing is subject to change without notice. Updated listing will be faxed/emailed periodically
to inform of new openings.
LOCATION: San Diego, CA
STATUS: ASAP!
POSITION: SAS/macros, UNIX, clinical trials, biotechnology
AVAILABLE POSITION: 1
DURATION: 1 year+
RATE: Open (DOE)
REQUIREMENTS:
The consultant will report directly to client's manager and assist them with general SAS programming
needs supporting Clinical team users. The consultant will assist with programming for one or more
Phase I studies. In addition, the consultant will assist with the following responsibilities:
Creation of analysis datasets, summary tables and data listings for phase I/II clinical trials
Performing QC and identifying inconsistencies in data which may affect interpretation of safety and
efficacy analyses.
Contributing to maintenance, changes, enhancements, validations and application of SAS and
Macros. Providing input for and assisting with maintenance of project-specific programming
conventions.
Skills/Experience Required:
Minimum of BS degree in statistics, mathematics, computer science or related field
Experience in pharmaceutical or biotech industry
Excellent SAS skills including knowledge of macro language
Some familiarity with UNIX would be helpful
Ability to work independently
Excellent organization, communication and analytical skills
LOCATION: Houston, TX
STATUS: ASAP!
POSITION: SAS, SAS/macros, Oracle, Data Warehousing
AVAILABLE POSITION: 1
DURATION: 1 year+
RATE: Open (DOE)
REQUIREMENTS:
Required Skills:
1. Expert knowledge of SAS (BASE, MACROS)
2. Ability to develop specifications from requirements.
3. Experience in development, testing, and implementation of SAS-based production systems.
Strong emphasis on ability to design reliable, maintainable code, knowledge of performance related issues.
4. Experience addressing data quality issues (i.e. identifying critical issues, designing detection and
correction procedures, designing robust code)
5. Familiar with UNIX and windows NT
6. Experience working with Oracle databases
7. Experience with SQL
Preferred Skills:
8. Knowledge of SAS Risk Dimensions or SAS/ETS
9. Knowledge of Data Warehousing
10. Experience in the oil/gas/energy industry
Job Description
Within an assigned functional area the consultant will:
11. Translate requirements into specifications and be capable of working on projects involving development
of integrated modules of code with complex business rules defining their linkages and execution.
12. Collaborate in addressing performance, reliability, and maintenance issues in system design.
13. Develop, test, and implement production code
14. Actively interact with Data and Systems groups to address (technical) interface issues.
Email:
hourly rates and availability. Questions and/or inquiries should be directed to (714) 530-6005 ext. 104
NOTE: This listing is subject to change without notice. Updated listing will be faxed/emailed periodically to
inform of new openings.
SAS DWH Datawarehouse Developer - ZURICH
For existing team we require a permanent SAS DWH Datawarehouse Developer with knowledge of German for Zürich.
You will have extensive knowledge of the SAP integration with SAS DWH Datawarehouse. Expertise in SAS programming
under HOST and UNIX. You will have extensive DataWarehousing experience and Internet, SAP and MS-Access on an
SAS platform.
Malcolm T. Smith
Email:
Email:
Local work permits and full assistance to relocate.

SAS Openings as of August 28, 2002 - Houston, TX
DataLogic Consulting Inc.
12966 Euclid St., Suite 450
Garden Grove, CA 92840
Tel: (714) 530-6005 x104
Fax: (714) 530-6129
Web: www.dlgi.com
Email:
Email:
your desired hourly rates and availability.
Questions and/or inquiries should be directed to (714) 530-6005 ext. 104
NOTE: This listing is subject to change without notice. Updated listing will be faxed/emailed periodically
to inform of new openings.
TEXAS:
LOCATION: Houston, TX
STATUS: ASAP!
POSITION: SAS, SAS/macros, Oracle, Data Warehousing
AVAILABLE POSITION: 1
DURATION: 1 year+
RATE: Open (DOE)
REQUIREMENTS:
Required Skills:
1. Expert knowledge of SAS (BASE, MACROS)
2. Ability to develop specifications from requirements.
3. Experience in development, testing, and implementation of SAS-based production systems.
Strong emphasis on ability to design reliable, maintainable code, knowledge of performance related issues.
4. Experience addressing data quality issues (i.e. identifying critical issues, designing detection
and correction procedures, designing robust code)
5. Familiar with UNIX and windows NT
6. Experience working with Oracle databases
7. Experience with SQL
Preferred Skills:
8. Knowledge of SAS Risk Dimensions or SAS/ETS
9. Knowledge of Data Warehousing
10. Experience in the oil/gas/energy industry
Job Description
Within an assigned functional area the consultant will:
11. Translate requirements into specifications and be capable of working on projects involving development of integrated modules of code
with complex business rules defining their linkages and execution.
12. Collaborate in addressing performance, reliability, and maintenance issues in system design.
13. Develop, test, and implement production code
14. Actively interact with Data and Systems groups to address (technical) interface issues.
Analysis Programmers: Charlottesville Virginia
PRA International is a Contract Research Organization with Offices around
the world. This posting is for our Charlottesville VA Trials
Management Center. We're looking for bright, energetic SAS programmers with
proven team skills and a desire to work in clinical trials. We offer
exposure to Oracle, SAS, Core Dossier, Documentum, and to Clinical trials
work. Of course, significant exposure to these fields of knowledge is highly
desirable, but not necessary. We strongly support certification, conference
participation, and career growth.
Lee Walke
Director, Analysis Programming
PRA International
4105 Lewis and Clark Drive
Charlottesville, VA 22911-5801 USA
Email:
Web: www.praintl.com

Regular Full-Time-Database Analyst - New York City
Title: Database Analyst
Location: New York City
Reports to: Director of Biostatistics
Coordinates with: Principal Investigators and Clinical Database
Manager for a medical research site
Duties and Responsibilities:
- Design, develop and maintain efficient research relational
databases
- Design, develop and maintain data entry forms for research
relational databases
- Develop and maintain VB and/or SAS code to maintain data
consistency and integrity
- Design, develop and maintain periodic and ad hoc summary reports
from relational databases
- Develop and maintain tuning, efficiency and backup protocols
- Create merged datasets for statistical analysis
Minimum requirements: Bachelor's degree in Computer Science or degree
in another field with experience in relational database design and
management (e.g. ACCESS, SQL Server and SAS experience a plus).
Forward Correspondence to
Dr. Jose M. Alvir at:
Email:
Or fax resume to: 212-263-3690 - No phone calls please.
Email:
Job openings - Rockville, Maryland
We have two openings for SAS programmers here at
KAI, a small medical research company in Rockville, MD.
1) We need someone quickly for a short-term assignment which may last several months. We would prefer someone
who can work on-site, but we could possibly work out other arrangements with the right person. For this job, we need
an experienced programmer, and familiarity with clinical trials would be an advantage.
2) We also need a permanent, full-time programmer to join our small SAS programming group. We would prefer 3 years
or more of SAS programming experience, but we would be willing to train the right person. A clinical or survey research
background would be helpful.
A college degree is a requirement for both positions.
Wanda Upole
SAS Programmer
KAI
6001 Montrose Rd., Suite 920
Rockville, MD 20852
(301)770-2730
Email:

Senior Biostatistician with clinical trials experience
Contract position in South San Francisco, CA
Job Number: C10272
Pay Rate: $70 to $80 per hour
Contract Length: 3 to 6 months
Contractor details:
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
Currently relocation expenses are not available for this position, but relocation
expenses are available for full-time positions.
We cannot work with candidates represented by third parties or agencies
Job Description:
You will work with the senior Biostatistics staff and clinical monitors on clinical
development plans, the design and conduct of clinical studies and in the evaluation,
interpretation and preparation of study results.
As part of a clinical assessment team, you will collaborate in the preparation and
review of clinical assessments.
For assigned clinical development project(s), you will provide statistically sound
experimental design and data analysis input to meet project objectives and FDA statistical requirements.
Review all project protocols, author protocol statistical analysis sections and generate study randomizations.
You will develop study analysis plans as a team member; and lead this effort for selected studies.
Review case report forms to ensure that protocol objectives are met and project standards are maintained.
Develop statistical programs as necessary to perform analyses, prepare data displays,
and verify data accuracy and validity.
Author statistical analysis results in the clinical study report.
With help from senior statistical staff, lead team members to author the report.
You will be responsible for seeing the report through the review process.
You will supply statistical input for BLA submissions and in response to FDA questions.
Provide support for investigator publications.
Keep abreast of new developments in statistics, drug development, and regulatory
guidance through literature review, workshop attendance, etc.
Candidate requirements:
Ph. D. in statistics/biostatistics with at least 2 years of clinical trials experience
Or, a Master's Degree in statistics/biostatistics with at least 5 years of clinical trials experience.
Experience with statistical software packages such as SAS and S-Plus.
Sound knowledge of theoretical and applied statistics.
Sound understanding of regulatory guidelines in a pharmaceutical research setting.
Effective communication skills.
Effective team contributor.
Contact Details
Name: Sara Schmidt
Tel: (415) 247 7700.
Email:

Salary range $90K to $120K
Please contact me at 860-547-4493
Linda Dikov
Email:
Applications Programmer (half-time) - RTP, NC
Applications Programmer:
CODA, Inc., located in RTP, seeks a half-time SAS programmer for epidemiology research setting.
Minimum job requirements: 2 years SAS programming, data management and
documentation, college degree. Must have experience in medical/health
research. Requires self-starter who adapts quickly to new applications
and works well in a team.
CODA, Inc. is a woman-owned, small business conducting research for NIEHS since 1994.
Apply by 09/20/02:
Programmer Search
CODA, Inc.
1009 Slater Rd., Suite 120
Durham, NC 27703
FAX: 941-9349
Salary dependent on experience
EOE M/F/H/V.
Email:
SAS Position in North Carolina
Looking for a strong SAS programmer with Statistical analysis experience.
MINIMUM REQUIREMENTS:
Bachelor's degree(Masters Preferred) in Public Health, Statistics or related field
Experience with SAS, including programming and statistical analysis required. Experience with the analysis of large and complex datasets is preferred.
Proficiency in the management of time and flexibility to meet demanding project timelines.
Substantial experience with the documentation of code or work processes
Excellent communication skills including proficiency in communicating technical information and concerns
Developed ability to use various PC software programs: Microsoft Project, Word, Excel, Access, and PowerPoint
Proficiency in the use of large computerized relational databases
Knowledge of statistics and project management skills are required.
Health care experience is desired but not required.
RESPONSIBILITES INCLUDE BUT ARE NOT LIMITED TO THE FOLLOWING:
SAS and other programming support ( SQL, UNIX, BRIO)
Design, develop, and recommend various programming techniques and tools for data extraction, transfers, manipulation, and reporting on multiple IT platforms (UNIX, PC)
Perform quality control and improvement processes
Design, conduct, and interpret statistical analyses
Interactions with internal and external customers
Location: North Carolina
Duration: 6 months contract
Minimum of 5 years experience with 3 years in the USA
Excellent communication skills needed
Email resume to
Harshi Krishnaswamy
Email:
for immediate consideration