For a confidential consultation call Doug Roberts on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
1207/06A
Contract Senior SAS Programmer
UK, Home/Office-Based
6 month+ renewable contract
Attractive Hourly Rate
Summary:
You will be responsible for designing and developing standard software and data structures, developing and executing statistical programs designed to analyse clinical trial information and participating in the development and maintenance of SOPs (including software validation, documentation, study archiving and others as needed).
Roles and Responsibilities:
Develop and execute statistical analyses of clinical trial data under the general guidance of a biostatistician. Design and develop computer programs that produce tables, figures, listings and derived datasets that summarize results of clinical trials.
Participate in the review of Case Report Forms (design phase), Statistical Analysis Plans, QC Specifications and Database Structures.
Assess data from clinical trials for consistency and accuracy. Develop and implement quality assurance software.
Ensure accuracy of all results and provide appropriate documentation.
Design and write standard maintainable, supportable, well- documented computer programs that are user-friendly and accessible.
Design and implement analysis file structures.
Review software written by programmer analysts in the department for accuracy and efficiency.
Monitor procedures for software validation.
Work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
Provide technical support to SAS users.
Other responsibilities as assigned.
Essential Skills & Capabilities:
Bachelor's of Science degree in a quantitative discipline (or training equivalent to) or equivalent work experience.
3+years full time SAS programming experience for Senior Programmer; experience must be in the pharmaceutical or biotechnology industry.
Familiarity with multiple software products and platforms.
Understanding of data structures, standard software and their implementation.
Knowledge of the drug development process (Phase I through IV) and general regulatory requirements.
Demonstrated leadership skills as well as ability to work independently and on a team.
Ability to serve as department representative at cross-functional meetings.
Good written and verbal communications skills.
For further details or a confidential conversation please contact me directly:
Doug Roberts
Researcher - Pharmaceutical, Healthcare & CRO Division
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
[log in to unmask]
http://uk.linkedin.com/in/dougroberts
Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician.
SEC Recruitment Ltd Company registered in England and Wales No. 5808613 - Registered Office: RDL House, 1 Chertsey Road, Woking, Surrey GU21 5AD.
IMPORTANT NOTICE: The information in this e-mail and any attached files is CONFIDENTIAL and may be legally privileged or prohibited from disclosure and unauthorised use. The views of the author may not necessarily reflect those of the Company. It is intended solely for the addressee, or the employee or agent responsible for delivering such materials to the addressee. If you have received this message in error please return it to the sender then delete the email and destroy any copies of it. If you are not the intended recipient, any form of reproduction, dissemination, copying, disclosure, modification, distribution and/or publication or any action taken or omitted to be taken in reliance upon this message or its attachments is prohibited and may be unlawful. At present the integrity of e-mail across the Internet cannot be guaranteed and messages sent via this medium are potentially at risk. All liability is excluded to the extent permitted by law for any claims arising as a result of the use of this medium to transmit information by or to SEC Recruitment Limited.
You may leave the list at any time by sending the command
SIGNOFF allstat
to [log in to unmask], leaving the subject line blank.
|