You will join a major international organisation, committed to the delivery of innovative drug development solutions to clients in the pharmaceutical and biotechnology industries. To meet the ongoing needs of the business, they are looking for a Statistical Programmer Analyst.
Statistical Programmer Analyst
Location M4 Corridor
The role of the post holder is to assist in the provision of a Statistical Programming service. The primary activity of the Statistical Programmer Analyst is to develop and review SASŪ programs and output for the management and reporting of clinical trial data and after sufficient experience, act as a Lead Programmer.
Key Responsibilities:
- Carry out all activities according to SOPs working within the framework of the Quality Management System and to Good Clinical Practice.
- Preparation and review of Programming Plans
- Participate in the Statistical Programming review of study related documentation
- Develop and review SAS programs and output as required for the management of clinical trial data
- Carry out electronic data transfer (both incoming and outgoing). Develop and review programs to ensure the data transfer has been produced to specification
- Set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities
- Review draft and final production runs for projects to ensure quality and consistency
- With sufficient experience assume the role of a Lead Programmer for assigned projects.
- Ensure the filing of study documentation is maintained to the standard required according to processes and acceptable for audit
- Ensure quality of personal work and the work of the team when acting as a Lead Programmer
- Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics
- When acting as a Lead Programmer provide input into resource assessments for programming activities
- Advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders
- Prioritise personal workload to meet specified completion dates.
- Assist with training, mentoring of Statistical Programmers under the supervision of senior Statistical Programming staff
- Participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually improved
You will be educated to degree level in computing, life science, mathematics or statistics. You will have gained approximately 18 months experience as a Statistical Programmer and a good understanding of clinical trial processes. Good problem solving skills, a proactive approach and a willingness to take decisions, are requirements for this role. You will also display a positive attitude at all times, promoting and contributing to a good team spirit.
To apply for this position please send a CV as a Word attachment to [log in to unmask] <mailto:[log in to unmask]>. Alternatively, call Julie Coates on 01707 280815 for a confidential discussion quoting Ref: RSAP04131JC. Please also provide examples where you have demonstrated the skills and competencies, which you feel, are required for this role.
For this job, we can only consider applications from those who already have the right to live and work in the UK.
Julie Coates
Consultant
Direct: +44 (0)1707 280815
RSA Pharmarecruit
For further information on RSA Pharmarecruit see our website: http://www.rsapharmarecruit.com
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