Displaying 20 results from an estimated 400 matches similar to: "New Bioinformatics Position with R Programming"
2010 Jul 29
0
Bioinformatics Position with Large Pharmaceutical in New Jersey
I currently have an opening with a large Pharmaceutical company in New Jersey. If you have any interest please contact Christina Kinchen at 800-684-9921 ext 220 or 407-548-0670 email: Ckinchen at smithhanley.com. We also have a great referral program if you know of anyone who is a fit. Please feel free to contact me with any questions.
Job Details:
--3+ years' bioinformatics research
2009 Aug 19
0
New SAS and R programming position with large Pharmaceutical in NJ
I have an opening for a Senior Programmer in Central New Jersey with a large Pharmaceutical company.
Senior Programmer needed to create applications for automating statistical analyses and creating reports. The candidate will generate user requirements, develop and write code, and take the lead in the validating the applications. The primary emphasis will be on creating applications to automate
2007 Oct 29
0
FW: Sr. SAS and R programmer needed in MA, NJ, or IL
-----Original Message-----
From: Christina Kinchen [mailto:ckinchen at smithhanley.com]
Sent: Thursday, October 25, 2007 5:05 PM
To: 'r-sig-jobs at r-project.org'
Subject: Sr. SAS and R programmer needed in MA, NJ, or IL
SAS Programmer III needed for large Pharmaceutical company in Chicago. The
individual can work in Chicago, New Jersey or Massachusetts. The ideal
candidate has extensive
2007 Oct 25
0
S-Plus or R programmer for Pharmaceutical Company
We currently have an opening for a S-Plus/R programmer at a large
pharmaceutical company.
Job Description:
S-Plus/ R Programmer -BS/MS in statistics - Solid S-Plus (or R) and SAS
programming skills required, minimum 1 year work experience writing
functions in S-Plus or R. SAS experience should include writing SAS macros
and creating and manipulating ODS datasets. Strong interpersonal and
2008 Mar 19
0
SAS/R position open with pharmaceutical in NJ/MA/IL
I currently have an opening with a Large Pharmaceutical Company for a Sr.
SAS programmer with extensive R experience. This position is in New Jersey,
but could possibly work out of Illinois or Massachusetts if necessary.
Please email me at ckinchen@smithhanley.com, or contact me via my website
link at http://www.smithhanleyconsulting.com/pharma/about/bios.asp?id=7 . I
can be called at 800-684-9921
2008 Aug 20
0
R and SAS Statistical position open with Large Pharmaceutical in New Jersey
I have 2 positions open with a top pharmaceutical company in New Jersey.
This position is not requiring pharmaceutical experience as long as the
candidate has strong SAS and R experience. In particular they are looking
for strong graphics experience in S-Plus/R (lattice or Trellis?TM graphics).
If you would like to learn more about this position please contact Christina
Kinchen at ckinchen at
2014 Jul 02
0
Work From Home Statistical Analyst Opening
We are currently seeking a Statistical Analyst to work for a large Pharmaceutical company in the US. This position is a Work From Home opportunity. If you meet the requirements below please send your resume to Christina.Kinchen at InventivHealth.com or call 407-548-0670.
REQUIRED:
* The ideal candidate will have strong R programming skills and 6 months, or more, work
2014 Jul 02
0
Work From Home Lead Statistician Opening
We are currently seeking a Lead Statistician to work for a large Pharmaceutical company in the US. This position is a Work From Home opportunity. If you meet the requirements below please send your resume to Christina.Kinchen at InventivHealth.com or call 407-548-0670.
A brief description is as follows:
Title of Position: Telecommuting LEAD STATISTICIAN
REQUIRED:
. The ideal candidate will have
2008 Aug 20
4
Looping over groups
Hello,
My R skills are somewhere between novice and intermediary, and I am hoping that some of you very helpful forum members, whom I've seen work your magic on other peoples' problems/questions, can help me here.
I have a matrix with the following format:
(i) individual plants comprising many different genotype groups (i.e., a plant is genotype 1 or genotype 2 or genotype 3, etc). The
2007 May 14
1
optim bug (PR#9684)
Full_Name: Christina Merz
Version: R version 2.5.0 (2007-04-23)
OS: mingw32
Submission from: (NULL) (213.70.209.132)
R> version
_
platform i386-pc-mingw32
arch i386
os mingw32
system i386, mingw32
status
2005 Jan 02
0
[Bug 2207] New: Listing of available sync-sets is very different with or without ssh
https://bugzilla.samba.org/show_bug.cgi?id=2207
Summary: Listing of available sync-sets is very different with or
without ssh
Product: rsync
Version: 2.6.2
Platform: All
OS/Version: All
Status: NEW
Severity: normal
Priority: P3
Component: core
AssignedTo: wayned@samba.org
2008 Nov 18
1
Tukey HSD following lme
Hi everyone
I'm using Tukey HSD as post-hoc test following a lme analysis. I'm
measuring hemicelluloses in different species treated with three
different CO2 concentrations (l=low, m=medium, h=high). The whole
experiment is a split-plot design and the Tukey-function from the
package multcomp is suitable for lme-analysis with random factors.
The analysis works fine but I get a non
2009 Oct 02
0
(no subject)
Dear R Community,
I am running GLM's within the "MASS" library. My data are overdispersed and
I am accounting for the overdispersion by using an ANOVA 'F' test instead of
ANOVA 'Chisq'. You will have to forgive me because I am new at this, but I
am not sure if R is conducting an ANOVA 'F' test appropriately. I was
hoping to explain this using my data
2008 May 26
0
use aov or lme for split plot design?
Dear all
I'm not sure if I did the right analysis for my specific split splot
design. We are
studying biomass increase with different CO2 concentrations with four
different
functional plant groups (e.g. grasses, herbs, broad-leafed trees and
conifers). Of each
functional plant group we have four species. The design is orthogonal.
The design is:
Blocks: 2 (climate chambers, called
2009 Sep 28
2
creating vectors from a list
Hi guys,
I have a list of 250 numbers as a result of using the ?by function!
List of 246
$ 0 : num [1:28] 22 11 31...
$ 1 : num [1:15] 12 14 9 ...
..
..
..
- attr(*, "dim")= int 250
- attr(*, "dimnames")=List of 1
The problem is that each list of 250 has different length! I would like to get the values of each list in a vector like vector_0 = (22,11,31,..), is this
2007 Jul 19
2
Subsetting dataframes
Dear all!
W2k, R 2.5.1
I am working with an ongoing malting barley variety evaluation within
Sweden. The structure is 25 cultivars tested each year at four sites, in
field trials with three replicates and 'lattice' structure (the replicates
are divided into five sub blocks in a structured way). As we are normally
keeping around 15 varieties from each year to the next, and take in 10 new
2009 Sep 29
1
Comparing vectors from lists
Hi guys,
I still did not solve my problem properly! I have to compare the values of two lists of 250 numbers as a result of using the ?by function!
List1 of 250
$ 0 : num [1:28] 22 11 31...
$ 1 : num [1:15] 12 14 9 ...
..
..
..
- attr(*, "dim")= int 250
- attr(*, "dimnames")=List of 1
List2 of 250
$ 0 : num [1:24] 20 12 22...
$ 1 : num [1:17] 11 12 19 ...
..
..
2005 Sep 29
2
memory issues with large data set
Hi,
I am running R 2.0.1.1. on Windows. It is a Dell Dimension with a 3.2 Ghz Processor and 4Gb RAM.
When using the ReadAffy() function to read in 97 arrays, I get the below error messages:
Error: cannot allocate vector of size 393529
Reached total allocation of 1024Mb: see help(memory.size)
When I use the comman "memory.limit(size=4000)" to increase the memory size to the
2004 Aug 01
2
Strange Problem with "proj" and "aov" for split-plot analysis output
I'm using R 1.8.1 on Red Hat Linux 9. I've worked out the linear model
decomposition by hand. Using "aov" with "Error" to fit a split-plot
model, I get very different results depending on whether I use the
"data" argument for "aov" or not. When I use the "data" argument, the
ANOVA table from "summary" is correct but the
2005 Feb 02
0
Samba 3.0 question, DOMAIN vs. SERVER method? Help!
Hello all!
We are attempting to get Samba-3.0.10 working on a new Solaris 8 machine in
preparation for upgrading an existing 2.2.8 installation (both use the
SMCsamba packages from SunFreeware.com). We copied over the smb.conf file
and the usermap from the Samba-2 installation, and seeing some weird
symptoms when Windows users try to connect to the new machine.
We ran "net join" to