Statistical Programmer II
Date Posted: Tuesday, 14th of February 2012
Salary: Circa £35,000
Start Date: 12 Mar 2012
Telephone: +44(0)1438 870028
Location: South East UK
Consultant Name: Priya Mukherjee
Sector: Clinical
Description
CK Clinical is recruiting for a Statistical Programmer II who will provide technical expertise for the conduct of clinical trials, and who will work with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data.
Key Accountabilities
• Deliver best value and high quality service
• Ensure quality control (QC) on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance^with corporate quality standards, WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.
• Assist in the coordination of project start-up activities, including Unix/PMED project area set-up,creation of global programs (e.g., setup.sas, formats.sas, etc.), tracking spreadsheets, and required documentation.
• Assist in the production and QC of derived dataset specifications, programming specifications, and other process supporting documents.
• Use efficient^programming techniques to produce derived datasets, tables, figures and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures and data listings.
• Check own work in an ongoing way to ensure first-time quality.
• Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to ensure traceability and regulatory compliance.
• Proactively participate in quality improvement initiatives.
• Develop wider knowledge of SAS and otherrelevant programming languages and processes within the GRO, Biostatistics, and Medical arenas.
• Provide relevant training and mentorship to staff and project teams as appropriate.
• Assist project teams in the resolution of problems encountered inthe conduct of their daily work.
Interested applicants should hold a BSc Degree in a Scientific discipline, Mathematics, Statistics, Computer Science OR Equivalent, together with proven experience of working within a CRO/Pharmaceutical/Biotechnology organisation. You will be proficient in SAS Programming and have knowledge of the programming and reporting process.
You will be able to demonstrate the ability to learn new systems and function in an evolving technical environment and to workwithin a team or independently.
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23703 in all correspondence.