j*****3
发帖数: 6 | 1 Anyone interested please send resume to j************[email protected] or apply
through the following link:
http://careers.peopleclick.com/careerscp/client_medtronic/exter
Position Description
Provide experienced, comprehensive technical expertise as part of the
Statistical Programming (SP) team to develop and maintain programs and
process methodology to meet internal and external clients’ needs. Plan and
lead the development of solutions to all statistical analysis programming
needs, particularly complex studies such as Premarket Approval (PMAs)
studies. Provide technical expertise and leadership to the Statistical
Programming department.
This role is eligible for a Telecommuter, within the U.S.A.
Position Responsibilities
Plans and coordinates statistical programming for complex studies
May integrate databases from multiple studies or sources
Reviews Statistical Analysis Plans from the programming perspective
Assists in data cleaning process
Programs analysis database manipulations and transfers of data for
internal and external clients
Programs, tests, documents, and validates statistical programs and
tools in accordance with SP standards and validation procedures
Serves as SP Lead representing Statistical Programming on the
corporate team
Develops and maintains good communications and working
relationships with teams and external clients
May interact with other SP team members and cross functional teams
to negotiate timelines, responsibilities, and deliverables
May serve as Project Manager or technical liaison with other
departments
May participate in relevant client presentations and proposal
development
Meets milestones as assigned
Assists in the development of training materials for departmental
and North America office use
Understands and complies with Standard Operating Procedures and
Work Instructions. Assists in developing, revising, and maintaining Standard
Operating Procedures and Work Instructions
Provides intermediate technical expertise in conjunction with
internal and external clients
Assists in the collaboration with data management team in
developing and implementing new technologies or software
Independently brings project solutions to SP teams
May Oversee the work of outsourcing partners and vendors at study
level
Mentors junior programming in departmental procedures and
developing technical and/or database expertise
Performs other duties as directed by SP management.
Basic Qualifications
• Bachelor’s degree in computer science, biostatistics or related
field with 4+ years of relevant work experience or Master’s degree with 2+
years of relevant work experience or equivalent.
• Has experience in clinical trial data submission to regulatory
agencies
KNOWLEDGE & SKILLS/COMPETENCIES
• Intermediate knowledge of Base SAS® is required. Average
knowledge of SAS/STAT, SAS Macro language, SAS/SQL, SAS/GRAPH, and SAS ODS.
• Good organizational, interpersonal, communication, and good
understanding of relational database are essential.
• Position requires a large amount of keyboarding involving repetitive
motions with fingers and sitting for prolonged periods of time.
Desired/Preferred Qualifications
• Knowledge of SAS on multiple platforms is preferred.
• Knowledge of statistics/biostatistics is preferred
• Knowledge of CDISC and electronic submission is desired
• Solid understanding of clinical trial research development process
is preferred. |
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