Senior Statistical Programmer
0

applicants

4478

No. Views

 
When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly, with supporting medical and drug data that will significantly advance the cost effectiveness and quality of healthcare provision. Of the world's top 50 best-selling drugs, Quintiles has helped to develop or commercialise every single one.
 
We are currently recruiting for a Senior Statistical Programmer
 
PURPOSE
Provide experienced technical expertise to develop process methodology for department to meet internal and external clients' needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
 
RESPONSIBILITIES
• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.
• Program and plan the integration of databases from multiple studies or sources.
• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, 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 statstical team lead for single complex studies or group of studies.
• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.
• Provide training and guidance to lower level staff.
• Knowledge of statistics, programming and/or clinical drug development process
• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language
• Good organizational, interpersonal, leadership and communication skills
• Ability to effectively manage multiple tasks and projects
• Excellent accuracy and attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
 
Additional Information
Location | | | Start Date 2013-06-11
Job Type Full Time
Salary Not Provided
Career Level Not Provided Relevant Work Experience Not Provided
Education Level Not Provided Job posted on 11-Jun-2013


Contact Information
Company Name Quintiles Telephone No Not Provided
Contact Name Site Link Not Provided
 

       

Latest Jobs

Senior Quality Specialist
Responsible for providing support to Operations staff in the implementation of and adherence to processes, controlled documents, tools and templates to enhance quality of deliverables. Activities may include: Identification of process gaps and/or improvement opportunities; process authoring and
Location Durham
Posted on 18-Jul-2013
Director, Product Management Platform
The Director, Platform Solutions will help drive the platform technology strategy, in partnership with Engineering, to help achieve the vision of providing a fully integrated eClinical suite to the biopharmaceutical market. This also includes the advancement of platform technologies, products,
Location Home Based
Posted on 18-Jul-2013
Medical Information & Technology Specialist(based in Prague or Berlin)
The role can be based in Berlin or Prague • Provide technical 'Super User' support for the system used by Medical Services Assist with the identification and co-ordination of standardised methodologies relating to the safety database and other Medical Service systems • Act as a liaison point
Location Berlin
Posted on 18-Jul-2013
Senior Biostatistician
• Provide broad statistical support, including trial design, protocol and CRF development on specific studies • Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Location Berlin
Posted on 18-Jul-2013
Senior Associate, Regulatory Affairs
Key Accountabilities 1. Provide technical support to team members of Regulatory Affairs Department to ensure that they have the required knowledge to fulfill their duties, including training. 2. Participate in and contribute to project bids, including client presentations. 3. Support the feasibility
Location Seoul
Posted on 18-Jul-2013
 

 
Home | My Account | Browse by company | Browse by category | Contact us | Terms | Privacy | FAQ