SAS II

Surrey  ‐ Onsite
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Keywords

Description

Core Responsibilities
Performs Quality Control to ensure that outputs meet quality standards and project requirements. Works with Programmer, Biostatistician, and other project team members to resolve discrepancies or any findings.

Develops specifications and mock-up display for outputs of any complexity according to statistical and sponsor requirement. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming, accurately defines all variables to be accepted by peer review and sponsor/requestor
with little rework

As the Lead Statistical Programmer, directs the programming activities of other programming personnel, and monitors progress on programming deliverables.

Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications,annotated CRFs, and SAS database design, and provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.

Participates in sponsor meetings, kickoff meetings, and bid defense meetings as Statistical Programming representative, as required by sponsor.

Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and Statistical Programming management and completes project programming activities within
timeframe allotted.

Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.

Conducts effective internal meetings appropriate in format, frequency and attendees, distributes relevant information in advance, ensures minutes are promptly and accurately distributed, follows action items through to completion, and maintains order and focus of meeting and works towards consensus.

Maintains well organized, complete, and up-to-date project documentation, testing, and
validation/quality control documents and programs in compliance with Company and sponsor standards.

Skills & Attributes

We are seeking candidates with the following key attributes:
BS, MS, or equivalent in Mathematics, Statistics, Computer Science, or related field.

Extensive experience in SAS programming or equivalent combination of education and experience.

You will also have:
Experience with clinical trials preferred.

If you are interested in hearing about this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV to or contact me on .

To find out more about Real please visit www.realstaffing.com
Start date
11/2013
Duration
12
From
Real Staffing
Published at
07.09.2013
Project ID:
595408
Contract type
Freelance
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