| Job Detail View |
| Job Title: |
Statistical Programmer
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| Job Number: |
220-2607
|
| Company |
ClinForce
|
| Skill Sets: |
Long term contract assignment; MS preferred |
| City: |
Upper Providence |
| State: |
PA |
| Region: |
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| Pay Rate: |
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| Recruiter: |
Catherine Zeier |
| Job Company: |
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| Job Description: |
Successful candidate will provide programming expertise (SAS) in the production of analyses, tabulations, graphics and listings from clinical trial data. Key responsibilities and skills include the following:
Contribute to the preparation of analysis plans
Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports, etc.
Contribute to the integrated clinical/statistical report and other similar documents
Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting
Perform QC/QA procedures on work performed |
| Job Detail View |
| Job Title: |
Statistical Programmer
|
| Job Number: |
208-5639
|
| Company |
ClinForce
|
| Skill Sets: |
MS degree in Biostatistics or related field; 3 years related experience within the Contract Research Organization (CRO) or pharmaceutical/clinical trials environment
|
| City: |
King of Prussia |
| State: |
PA |
| Region: |
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| Pay Rate: |
|
| Recruiter: |
Holly Price |
| Job Company: |
|
| Job Description: |
Successful candidate will provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics and listings from clinical trial data. Key responsibilities and skills include, but are not limited to the following:
Contribute to the preparation of analysis plans
Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports and other similar reports
Contribute to the integrated clinical/statistical report and other similar documents
Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting
Perform quality assurance procedures on work performed by others
|
| Job Detail View |
| Job Title: |
Statistical Programmer
|
| Job Number: |
220-2634
|
| Company |
ClinForce
|
| Skill Sets: |
3+ years experience within the clinical research industry; MS Degree required; Experience in reporting of clinical trials data in pharmaceutical industry using SAS is extremely important; Must have good communication skills; Experience with ISS and ISE reporting is helpful |
| City: |
King of Prussia |
| State: |
PA |
| Region: |
|
| Pay Rate: |
|
| Recruiter: |
Catherine Zeier |
| Job Company: |
|
| Job Description: |
Successful candidate will provide programming expertise (SAS) in the production of TLGs from clinical trial data. Key responsibilities include the following: contribute to the preparation of SAPs, prepare/document and test required programs and procedure data displays for inclusion in integrated clinical statistical reports, etc. Contribute to the integrated clinical/statistical report and other similar documents. Ensure analysis data and programming code meet regulatory and company standards. Perform QC/QA procedures on work performed by others. |