Dear AllStat,
CK Clinical is a leading clinical recruitment company handling jobs in clinical research and drug development. Our clients include some of the top Pharmaceutical and Biotechnology companies from around the world and our reputation for honesty and integrity is well known. We offer contract and permanent job opportunities within Clinical Data Management, Clinical SAS Programming, Clinical Statistics, Clinical Coding, CRF Design, Database Build, and EDC Technology.
We are currently recruiting for a contract Statistical Programmer to work for a reputable Pharmaceutical company based in the UK. This is an initial 6 months contract with a view to be extended, and even become permanent towards the latter end of next year. Rates on offer are competitive and flexible and will be discussed upon application.
The purpose of the role is to provide a comprehensive statistical service for the Company and be responsible for all statistical aspects of the 5-6 clinical trials to which you will be independently managing.
The main duties include:
* Designing statistical studies for the analysis of clinical trials; formulating the hypotheses and objectives
* Providing a statistical quality control service while studies are in progress
* Assessing the impact on the statistical analysis of changes made during the study
* Performing the statistical analyses of clinical trials and answer statistical queries on the analysis or results
* Ensuring that the case report forms capture the data in the format most suitable for the statistical analysis
* Deciding with Project Team which subjects will be included in relevant analysis.
* Developing a written strategy for the statistical analysis of the trial
* Reviewing and helping generate papers from the results of the clinical studies
* Documenting all statistical analysis programs
* Maintaining knowledge of Standard Operating Procedures (SOPs), and ICH guidelines and take responsibility for those relating to statistical issues
* Keeping abreast of new developments in statistical methodology
* Producing material that is clear, concise and complete.
Interested applicants will hold a minimum of an MSc in Medical Statistics (Or equivalent) with proven experience of working within the Pharmaceutical industry. You will hold excellent SAS Programming skills with a good understanding of CDISC. You will also have excellent verbal and written communication skills whereby you can work well independently and as part of a team. A full job description can be provided upon request.
For a confidential discussion or immediate consideration, please contact Priya Mukherjee on 01438 870028 or email [log in to unmask]
Best wishes,
Priya
Priya Mukherjee BSc (Hons) MRec CertRP
Senior Consultant
CK Clinical Limited
9 High Street
Stevenage Old Town
Hertfordshire
SG1 3BG
DD: +44 (0)1438 870028
Tel: +44 (0)1438 743047
Fax:+44 (0)1438 723800
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