| Date: | Sun, 2 Jan 2005 15:12:05 -0800 |
| Reply-To: | Deb <webresearch@QWEST.NET> |
| Sender: | "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU> |
| From: | Deb <webresearch@QWEST.NET> |
| Organization: | http://groups.google.com |
| Subject: | JOB: Clinical Programmer / Seattle |
| Content-Type: | text/plain; charset="iso-8859-1" |
ICOS Corporation, based in Seattle, Washington, has spent more than a
decade building a world-class research and development organization.
ICOS' lead product, Cialis® (tadalifil), for the treatment of
erectile dysfunction, recently received US FDA approval and is
currently launched in over 50 countries worldwide. ICOS is committed
to advancing science in the areas of protein based and small molecule
therapeutics.
As a clinical programmer, you'll collaborate with biostatisticians
and other research personnel in the analyses of clinical trials.
Responsibilities include:
- Reviewing all table specifications and producing table shells for
CSR final listings, summaries and graphical figures
- Designing and develop generalized reporting programs and macros
- Validating program output
- Documenting and archiving results
- Coordinating outsourced 3rd party DSMB reporting; validating
clinical reporting data transfers
- Exploring relevance of CDISC standards and XML requirements of
electronic submissions to the FDA
- Contributing to and supporting programming standards within
Biometrics
Requirements include:
- 3+ years of scientific programming experience, using SAS and other
packages for statistical summaries and analyses
- 2+ years of relevant experience in clinical trials reporting using
multiple features of SAS in the pharmaceutical or biotech industry
- Demonstrated knowledge of clinical data structures, algorithmic
design, relational database design and technical project planning
- Masters in Computer Science, Statistics or natural sciences and 3+
years relevant experience or Bachelors in Computer Science, Statistics
or natural sciences and 4+ years of relevant experience
Other required attributes:
- Ability to use personal computer 6-8 hours / day
- Ability to work independently and creatively on multiple clinical
study reporting projects
- Attention to technical details and interest in learning new
techniques
- Ability to document clearly and communicate orally in group meetings
- Ability to liaise with other technical staff and consultants
Pluses include:
Knowledge of PC level programming and communication between platforms
ICOS offers a highly competitive compensation package and a friendly,
collaborative culture that values personal initiative and professional
achievement.
The employee benefit package includes:
- Education assistance and continuing education opportunities
- Medical, dental, life, disability, long-term care insurance
- 401(k) plan and stock options
- Paid vacation, sick leave and holidays
- Automobile purchase, Barnes & Noble, Dell and fitness club discount
programs
- Auto, homeowner and rental insurance discount programs
- Credit union and Costco memberships
- On-site early education program to serve employee's children
- Ergonomic offices
- Casual dress, company mixers, organized sports teams
- Annual golf tournament, company picnic and children's holiday
"cookie party"
- On-site dry cleaning services, financial planning/counseling
services and flu shots
To learn more about ICOS' employee benefits, work environment,
philosophies, attributes, financial information and exciting research
projects, visit www.ICOS.com.
For immediate consideration, please e-mail your updated resume to
webresearch@qwest.net ASAP. If you are not interested in this
position, but know others who may be, please do not hesitate to forward
this information to them.
Thanks for you time and consideration!
Deb Hester
webresearch@qwest.net
ICOS Recruiting Team
(866) 324-0705 (toll-free)
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