Contract Senior Biostatistical Programmer
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Job Type | Temporary / Contract |
Location | Berkshire |
Area | South East, UK |
Sector | Clinical Research |
Salary | See Job Description |
Currency | GBP |
Start Date | ASAP |
Advertiser | remoteapi |
Job Ref | BBBH634_1513969808 |
Job Views | 179 |
- Description
Are you ready for an amazing new career in 2018 ?
Contract Senior Biostatistical Programmer
Pop science is delighted to offer the position of Contract Senior Biostatistical Programmer.Our client is based in Berkshire with Specialised expertise in addressing unmet needs in the areas of analgesia, dermatology, haematology/oncology, medical device, neuroscience, paediatrics, and rare disease. We're looking for someone amazing who wants to join this dedicated team as a Senior Biostatistical Programmer (Contract or permanent )
Here's an idea of what you will be doing:- Oversee the successful operation of one or more groups within Biostatistics.
- Maintain responsibility for all assigned projects and direct reports.
- Mentor associate managers, along with other employees.
- Participate in informal business development if required.
Some of your responsibilities as a Senior Biostatistical Programmer:- Develop SAS programs to generate listings, tables and figures as outlined by mock TLF shells
- Perform quality control (source code review, double-programming and log review) of SAS programs
- Develop SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications
- Preparing specifications for CDISC and other analysis data sets
- Assist Data Management with SAS programming needs
- Act as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team
You should recognise yourself here if you want to apply:- Minimum BS from accredited college or university, in statistics, IT, mathematics
- Must have extensive of experience in SAS programming within the clinical trials.
- Prior experience using computerized information systems preferred.
- Knowledge of ICH and local regulatory authority drug research and development regulations preferred.
- Demonstrated working knowledge of data processing, database design and organization in clinical data environment
- Demonstrated working knowledge of basic clinical trial design and analysis principles
- Working knowledge of CDISC standards and application of these standards to projects
- Working knowledge and understanding of advanced statistical concepts to program analysis datasets and tables which include descriptive and standard/complex inferential statistics
- Fluent verbal and written English
- Excellent team player, collaborative and able to build an effective team.
- Ability to work effectively in a fast-paced environment with changing priorities.
- Customer focused as a priority in approach to work both internally and externally.
- Positive, results orientated
- Attention to detail and ability to independently work on stand-alone Biostatistical projects with general supervision
If this sounds like you or even someone you know please contact Bryan Mackie right away Tel : 01273 729819 OR Email bryan@pop-science.co.uk
We can offer this as a permanent or contract opportunity .Pop Science are an innovative, personal and experienced recruitment and staffing consultancy. Our aim is to make science more popular by championing careers in clinical and scientific research, technology, engineering, maths and more. Whether you want a permanent job, a contract role or even a change in perspective with some volunteering, contact us and let us help you. We support working practises that promote happiness at work.
We're an experienced, skilled team with personality; we have a passion for science, and drive and enthusiasm to make a difference to you.
Find out more at Pop Science - Recruitment