Location : Home Based or Office Based Anywhere in US-1308003
Organization
: USA02 - US Clinical Development Svcs
Description
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.
The
Sr. Statistical Programmer or Stat Programmer 2 will provide
experienced technical expertise as part of the Global Functional
Resourcing (GFR) 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 GFR 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. and
will be hired at a Grade 30 or 31 depending upon experience of
candidate.
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.
Qualifications
•
Masters degree or educational equivalent in computer science or related
field and 3 years relevant experience; Bachelor's degree or educational
equivalent in computer science or related field and 4 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
• 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
• 2+ years generating NONMEM datasets preferred
• 2+ years experience with CDARs system preferred
see https://quintiles.taleo.net/careersection/10080/jobdetail.ftl
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