Fforde are seeking a contract CDISC SAS programmer for a 6 month contract based from home:
Below is the generic description, please email or call Natalie Fforde for more information:
[log in to unmask]
tel: 07769 700 222
The Biostatistics Department is responsible for the statistical aspects of clinical trials, including experimental design, designing and implementing standardized clinical data solutions, statistical analysis/programming, and reporting.
Additional Responsibilities :
• Development and delivery of loading external data
• Development and delivery of observational datasets to Sponsors and Clients Biostatistics.
• Development and delivery of CDISC compliant and sponsor defined data structures.
• Development and delivery of sponsor defined data management listings/reports
• Contributes to the creation of study level documentation and files according to departmental policy and regulatory requirements.
• Liaison with Data Management and Biostatistics on database specifications, timelines and quality requirements.
Experience and Qualification
• Appropriate computer-related qualification or equivalent
• Understanding of data structures is required as well as a basic understanding of the development and use of standard programs.
• Must work independently as well as part of a team and have good problem solving skills, attention to detail, verbal and written communications skills.
You may leave the list at any time by sending the command
SIGNOFF allstat
to [log in to unmask], leaving the subject line blank.
|