S
sarah Fernandes
Pls go thru this requirement and let me know if you are ok with it.
Pls send resumes to (e-mail address removed)
Or call 732-372-7051
Location : Bridgewater, NJ. Duration : 1 year.
Face to face is required. No expense paid for face to face. Client
prefers locals.
SAS Clinical Programmer
Overview of Position:
1. Generate data listings, tables and figures (TFL) from clinical
data, using SAS or other statistical software
2. Create SAS tools to output TFL directly into clinical study reports
3. Review clinical protocols, SAP and case report forms
4. Create SAS tools to extract data from various sources, including
CRFs, labs, cooperative groups, imaging, IRC, DSMB, IVRS
5. Merge and/or restructure data to create derived analysis datasets,
data warehouse, ISS, ISE, CRTS, in support of regulatory submissions
6. Provide programming support to in-house and externally hosted
electronic data collection (EDC) systems
7. Provide programming support to produce CDISC compliant databases
(e.g. STDM, ODM, ADAM) for regulatory submissions
Requirements:
B.S. or M.S. in MIS, Statistics, Computer Science, Chemistry or
related fields
Two years experience in statistical programming for the analysis of
clinical data, preferably within biotech/pharma
Very good knowledge of SAS programming
Good communications and writing skills
Kindly refer some of your friends with the same skill. Your help would
be appreciated.
Please let me know if you would be interested. Call on 732-372-7051
or email your resume on (e-mail address removed)
Thanks,
Sarah
Pls send resumes to (e-mail address removed)
Or call 732-372-7051
Location : Bridgewater, NJ. Duration : 1 year.
Face to face is required. No expense paid for face to face. Client
prefers locals.
SAS Clinical Programmer
Overview of Position:
1. Generate data listings, tables and figures (TFL) from clinical
data, using SAS or other statistical software
2. Create SAS tools to output TFL directly into clinical study reports
3. Review clinical protocols, SAP and case report forms
4. Create SAS tools to extract data from various sources, including
CRFs, labs, cooperative groups, imaging, IRC, DSMB, IVRS
5. Merge and/or restructure data to create derived analysis datasets,
data warehouse, ISS, ISE, CRTS, in support of regulatory submissions
6. Provide programming support to in-house and externally hosted
electronic data collection (EDC) systems
7. Provide programming support to produce CDISC compliant databases
(e.g. STDM, ODM, ADAM) for regulatory submissions
Requirements:
B.S. or M.S. in MIS, Statistics, Computer Science, Chemistry or
related fields
Two years experience in statistical programming for the analysis of
clinical data, preferably within biotech/pharma
Very good knowledge of SAS programming
Good communications and writing skills
Kindly refer some of your friends with the same skill. Your help would
be appreciated.
Please let me know if you would be interested. Call on 732-372-7051
or email your resume on (e-mail address removed)
Thanks,
Sarah