Biostatistician with SAS Programming II (JOB ID- 5205865)

Artech Information System LLC; Bridgewater (MA); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading staffing company in Massachusetts seeks a Biostatistician to support early phase clinical trials. The role involves statistical operations, data review, and analysis, requiring a Master's in statistics or biostatistics and proficiency in SAS programming. Ideal candidates will have 2+ years of experience in the pharmaceutical industry, particularly in Phase 1 trials. This is a contract position offering opportunities to collaborate within clinical study teams.

Qualifications

• Proficient in SAS programming including Data steps, PROC ANCOVA, PROC MIXED, and PROC GPLOT.
• 2+ years of experience in the pharmaceutical industry, preferably with Phase 1 trials.

Responsibilities

• Perform and carry out statistical operations supporting early phase clinical trials.
• Contribute to statistical components of clinical study reports.
• Collaborate with study team members on statistical activities.

Skills

SAS programming

Statistical analysis

Communication skills

Attention to detail

Time management

Education

MS degree in statistics or biostatistics

Job description

Biostatistician with SAS Programming II (JOB ID- 5205865)

• Contract

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

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.