CK Clinical have a number of open positions within SAS Programming & Statistics on both a permanent and contractual basis. Please find below a selection of vacancies on offer:
Associate Director, Biostatistics
An established Pharmaceutical organisation is recruiting for an Associate Biostatistics Director to provide statistical expertise to the clinical development program for assigned projects, ensuring scientifically valid conclusions are drawn with respect to efficacy and safety of the compound under development. You will also take full responsibility for clinical development plans and interactions with regulatory authorities. Within the role, you will also be expected to lead a team of Biostatisticians on complex projects and manage external vendors and CROs. You will hold an MSc (OR equivalent) in Statistics with proven experience in applying Statistical methods in clinical research. You will also have advanced knowledge of SAS Base/SAS Stat programming.
Senior Project Biostatistician
A reputable Pharmaceutical organisation is seeking a Statistician to take responsibility for Biostatistic study design/analysis support on projects, handling output orientated projects of a limited technical nature and working together with statistical programmers. You will be involved in leading project analyses to support study findings/designs, including computational work and presentation of clinical study results. You will also contribute to the development of Clinical Development Plans, Protocol Development and Statistical Analysis Plans. You should be qualified to MSc level (Or Equivalent) in a Statistics discipline and have proven experience of working for the Pharmaceutical industry.
This established Biotechnology Company is recruiting for a contract Biostatistician to work within the Oncology therapy area. You will be involved in preparing statistical analysis plans; creating statistical analysis program specifications; writing, validating and documenting statistical analysis programs; performing statistical analyses and preparing study report tables, listings, graphs and reports; interpreting and presenting results; and maintaining up-to-date study documentation. You will hold proven industry/academia experience and knowledge of SAS.
Senior/Principal SAS Programmer
In this fast-paced clinical trial environment, you will play a vital role applying programming knowledge to the analysis and reporting of clinical trial data, covering a wide range of therapy areas. You will also be involved in the design and maintenance of a SAS Program library and for the creation of new tools and processes. You will have proven experience as a SAS Programmer within the Pharmaceutical industry, and hold experience of mentoring junior programmers.
A well-established Pharmaceutical company is recruiting for a Clinical Programmer to give programming support for pharmacokinetic and modelling & simulation projects. You will be involved in validating PKS data-sets for standard, non-compartmental PK analysis, final delivery of PK parameters, and for the programming of data-sets for population PK, PK/PD and PK/Safety analyses. You should hold proven previous experience in PK/Programming, working for either a Pharmaceutical/Biotechnology/CRO.
Please feel free to contact me on +44(0)1438 870028 for a confidential discussion or further information, or email me an updated copy of your CV to: [log in to unmask]
I look forward to hearing back from you.
Priya Mukherjee BSc (Hons) MRec CertRP
CK Clinical Limited
9 High Street
Stevenage Old Town
DD: +44 (0)1438 870028
Mobile: +44 (0) 7714 288632
Tel: +44 (0)1438 743047
Fax:+44 (0)1438 723800
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