The Clinical Development Services division of Quintiles has more
depth of therapeutic expertise and a broader range of services than any
other service provider. We conduct both US and Global trials in all
therapeutic areas. In fact, Quintiles conducts more clinical trials than
anyone else in the world. Become involved in work that improves the
quality of life for people around the globe. Let your career soar! We
are seeking an enthusiastic Sr. Statistical Programmer or Stat
Programmer 2.
You will provide experienced technical expertise as part of the
Global Biostatistics/Customer Solutions PK/PD Programming team to
develop process methodology for the department to meet internal and
external clients’ needs. Plan and coordinate the development of
integrated programming solutions serving the full spectrum of
statistical analysis needs. Provide technical expertise and leadership
to the Customer Solutions department. Provide internal consulting
services, including specifications and user needs analysis for complex
project or client requirements.
This position can be home-based or office-based anywhere in the U.S. or Canada
RESPONSIBILITIES
• Program, plan and co-ordinate the following for complex
studies: (i) the programming, testing, and documentation of statistical
programs for use in creating NONMEM data files, (ii) the transfers of
data for internal and external clients, (iii) the programming of
database quality control checks, and (iv) the integration of databases
from multiple studies or sources.
• Develop, plan, and co-ordinate
programming documentation including plans and specifications, as
appropriate, for complex studies.
• Perform, plan and co-ordinate the
development, implementation and validation of new process technologies,
macros and applications.
• Fulfill project responsibilities at the level of lead for single complex studies or group of studies.
• Manage project budget and resource requirements and provide training/guidance to lower level staff.
.
Masters
degree or educational equivalent in computer science or related field
and 1 years relevant experience; Bachelor's degree or educational
equivalent in computer science or related field and 3 years relevant
experience; or equivalent combination of education, training and
experience
• Knowledge of statistics and clinical drug development process required
•
Knowledge of electronic submissions (including: knowledge of data
submission structures and requirements; experience in creating relevant
hyperlinks, etc)
• Advanced knowledge of statistical computing applications such as Base SAS, SAS/STAT and SAS Macro Language
• Good organizational, interpersonal, leadership, communication skills and multi-tasking abilities
• 1 year generating NONMEM datasets preferred but not required
• 1 year experience with CDARs system preferred but not required
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