Statistician - Scientific III
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Job description
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. Analysis Standards Associate - Statistician III Consultant Correct Location- TITUSVILLE, NJ (System Error)
Summary
The Analysis Standards Associate provides operational expertise in developing and managing analysis standards for clinical research. The role of the Analysis Standards Associate is to work with business stakeholders to align standards with business needs, provide standards guidance to content subject matter experts (SMEs) developing or updating standards content, review and QC standard SAS code, and support and align with relevant industry standards.
Key Responsibilities
- Work with business stakeholders to define, review, QC, and maintain standard statistical requirements aligned with business needs and industry standards
- Review and QC ADaM dataset and result metadata aligned with documented statistical requirements and industry standards
- Review and QC SAS programs and macros that create standard ADaM datasets and tables, figures, and listings based on documented statistical requirements
- Develop, review and maintain documentation describing standards and related processes and business rules
- Provide support for business stakeholders implementing standards including communications, training, Q&A, compliance and usage metrics
- Assist with coordination of standards development projects
- Assist with management, assessment, and execution of change requests
- Assist with maintenance of the standards repository
Qualifications
and Competencies
- BS/
- BA degree in statistics (preferred), computer science, mathematics, or other scientific field 5+ years as a statistician or similar position with clinical research analysis and reporting responsibility in a biopharma or CRO environment Basic knowledge in SAS programming with experience developing programs for QC/validation purposes
- Solid understanding of the principles and practices of clinical research analysis and reporting with Statistical Analysis
- Plan development experience Basic knowledge of relevant industry standards (ie, ADaM and SDTM with focus on ADaM specifications experience ) and solid knowledge of regulatory requirements
- Strong English verbal and written communication skills
- Experience working in a virtual team environment with good collaboration, organizational, communication, and problem-solving skills
- Ability to prioritize tasks and work effectively in a fast-paced multi-project environment
- BS/
- BA degree in statistics (preferred), computer science, mathematics, or other scientific field Regards, Akriti Gupta Associate Recruiter (Clinical / Scientific Division) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: 973.967.3409 | Fax: 973.998.2599 Connect with us on - LinkedIn | Facebook | Twitter