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Biostatistician with SAS Programming II
Ref No.: 16-03864
Location: Bridgewater, New Jersey
Position Type:Contract
Start Date / End Date: 10/24/2016 to 04/24/2017
Job Title: Biostatistician with SAS Programming II
Job Category: Clinical
Job Location: Menlo Park, CA
Job Duration: 3 Months
Interview Type: Face to Face
 
Duties:
Job Description (Contractor) MAX BILL 105/hour

The contractor statistician, reporting to the manager of the group, will perform and carryout statistical operations supporting early phase clinical trials. The work include mainly performing data review and statistical analysis, contributing to the statistical components of clinical study reports, participating in clinical study team meetings, and collaborating with study team members (study clinician, trial manager, data manager, clinical pharmacologist, pharmacokineticists, etc.) on any study related statistical activities. As needed, he/she may lead or participate in the development of SAP and TLG shells, validating analysis programs according to the SAP.

Qualifications

A MS degree in statistics or biostatistics with 2+ years’ experience in pharmaceutical industry is required; experience in Phase 1 trials is preferred. The candidate should be proficient in SAS programming (eg., Data steps, PROC ANCOVA, PROC MIXED, PROC GPLOT, etc.), have good communication skill, pay attention to details, able to manage tasks and deliverables with agreed timelines in mind, and work well in a team environment.

Skills:
Job Description (Contractor)

The contractor statistician, reporting to the manager of the group, will perform and carryout statistical operations supporting early phase clinical trials. The work include mainly performing data review and statistical analysis, contributing to the statistical components of clinical study reports, participating in clinical study team meetings, and collaborating with study team members (study clinician, trial manager, data manager, clinical pharmacologist, pharmacokineticists, etc.) on any study related statistical activities. As needed, he/she may lead or participate in the development of SAP and TLG shells, validating analysis programs according to the SAP.

Qualifications

A MS degree in statistics or biostatistics with 2+ years’ experience in pharmaceutical industry is required; experience in Phase 1 trials is preferred. The candidate should be proficient in SAS programming (eg., Data steps, PROC ANCOVA, PROC MIXED, PROC GPLOT, etc.), have good communication skill, pay attention to details, able to manage tasks and deliverables with agreed timelines in mind, and work well in a team environment.

Education:
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Job Description (Contractor)

The contractor statistician, reporting to the manager of the group, will perform and carryout statistical operations supporting early phase clinical trials. The work include mainly performing data review and statistical analysis, contributing to the statistical components of clinical study reports, participating in clinical study team meetings, and collaborating with study team members (study clinician, trial manager, data manager, clinical pharmacologist, pharmacokineticists, etc.) on any study related statistical activities. As needed, he/she may lead or participate in the development of SAP and TLG shells, validating analysis programs according to the SAP.

Qualifications

A MS degree in statistics or biostatistics with 2+ years’ experience in pharmaceutical industry is required; experience in Phase 1 trials is preferred. The candidate should be proficient in SAS programming (eg., Data steps, PROC ANCOVA, PROC MIXED, PROC GPLOT, etc.), have good communication skill, pay attention to details, able to manage tasks and deliverables with agreed timelines in mind, and work well in a team environment.

Hrs per Wk: 40.00
Hrs per Dy: 8.00