Description
This is a home based opportunity anywhere in North America.
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 Statistical Programmer 2/Sr. Statistical Programmer who
will provide advanced technical expertise to develop and maintain
programs to meet internal and external clients' needs. Plan and lead the
development of project-related solutions to the full scope of
statistical programming tasks. Provide technical expertise to the
Statistical Programming department.
RESPONSIBILITIES
· Perform
and plan: the programming, testing, and documentation of programs for
use in creating statistical tables, figures and listing, the programming
of analysis dataset (derived datasets) and transfer files for internal
and external clients. and the programming quality control checks for the source data and report the data issues periodically.
· Detect
errors in detail, corrects them (e.g., reviews tables/listings, edit
checks output and SAS programs to ensure quality of deliverable) and
report it to appropriate personals (internal or external clients)
· Provide
advanced technical expertise in conjunction with internal and external
clients, and independently bring project solutions to SP teams and
Statistical Programming department.
· Perform and plan the development, implementation and validation of new process technologies, macros and applications.
· Fulfill project responsibilities at the level of technical team lead for single studies, under supervision.
· Understand timelines for and milestones affecting their work and alert supervisor to potential slippage.
· Provide training and mentoring to SP team members
Qualifications
REQUIRED
· Masters
degree in computer science or related field and 1 year relevant
experience; Bachelor's degree in computer science or related field and 3
years relevant experience; or equivalent combination of education,
training and experience
· Knowledge of statistics, programming and/or clinical drug development process
· In-depth
knowledge of applicable clinical research regulatory requirements;
i.e., Good Clinical Practice (GCP) and International Conference on
Harmonization (ICH) guidelines
· Ability to implement programming specifications, as appropriate
· Ability to estimate programming scope of work and assist in communicating project status
· Working knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
· Familiarity with SAS Drug Development (SDD) and Clinical Data Integration (CDI) would be preferred
• Familiarity with SAS Drug Development (SDD) and Clinical Data Integration (CDI) would be preferred
• Good organizational, interpersonal, leadership, communication skills and multi-tasking abilities.
Primary Location
: USA-Kansas-Overland ParkOrganization
: USA02 - US Clinical Development Svcs
We look forward to the prospect of working
with you! Please apply on-line at: http://www.quintiles.com/.
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