SAS Programmer Contract, Biotech, CDISC
6-12 months, Day Rate Contract
A role working for one of the leading Pharmaceutical Employers within a great culture of excellence and trust. We're looking for an experienced SAS programmer^who has worked in clinical research within a CDISC compliant environment with biological/human health research data
In this role you can work from home after orientation. That said your customers are global and to perform you must be conversant with working within an international matrix, dealing with global stakeholders and someone who can manage relationships and expectations working in English by 'phone and email in the main.
Orientation will be in the UK HQ and you will be required to^spend 3-4 weeks in the office 3 days per week for this. We can consider EU based nationals who have good English language skills the cost of office working and attendance can be built in to a rate. Our client MAY consider a 4 day working week for the right person. We cannot consider individuals who have not worked in a sector where SOPs, regulatory compliance and human health is apparent or individual requiring sponsorship.
Programming aspects will include but not be limited to:
Clinical^Trial and epidemiology data manipulation
Analysis and reporting of clinical trial and observational data.
Specifically, CDISC compliant SDTM and ADaM dataset creation; table, figure and listing generation; program validation and documentation; and output verification.
Work is to be performed in a global team environment, where team members may be distributed across regions and time-zones and end of day commitment can be frequent
Essential Skills & Qualification
BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, or work experience equivalent
Specialist relevant programming experience in a clinical development environment
Excellent SAS v9 data manipulation, analysis and reporting skills
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
Ability to work effectively and successfully in a global team environment.
Excellent oral and written communication skills Ability to provide quality output and deliverables, in adherence with aggressive timelines
Willingness and ability to learn and follow standard processes and procedures Willingness to work^flexibly and proactively manage workload whilst working within and taking direction from a US-led team
Software Competence: MS Office, MS Project, SAS
Valid Driving License: Not Required
Working Language(s): English
Requirement for Business Travel: Rare
Flexible Working Hours: Yes but FTE or 4 days per week minimum
Employer: Pharmaceutical Company via an agency
Employment Type: Agency Contract
Hours: 1.0 - 0.8FTE can be considered
Contract Term: 6 months rolling term
Location: Location Independent
Plan Start Date: Latest 1st October 2012 but aply now to secure a role
Contract Benefits: Day Rate inclusive of benefits
Data Manager, Coding, Clintrial, Oracle, SAS, Statistician, Statistical Analysis, ANOVA, WinNonlin, SPSS, Clinical Study Report, CSR, CDISC, SDTM
Assigned Consultant: Ann Maloney at CSL Recruitment on 01932 234 689
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs; applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not^receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day^rate if you are a new candidate.