Statistical Programmer x3
Switzerland
Permanent
£Negotiable
Responsibilities;
* Provide input towards study protocol development, CRF design and data structure tables, listings and figures for clinical trials and submission activities
* Program analysis datasets, pooled datasets, tables, listings, and figures for clinical trials according to specifications
* Participate in the selection of CROs and supervise the statistical reporting activities of the CROs
* Close liaison with the study team including; Statistics, Clinical and Data Management
Qualifications;
* BSc in Statistics or computing with an MSc in Statistics an advantage
* Over 5 years statistical programming experience from a Pharmaceutical/CRO environment
* Excellent SAS knowledge
* Good Communication and Organisational skills
Note: This is an English speaking office.
If you feel you are well suited for this role please do not hesitate to contact us.
Kind Regards
Hannah Merchant
Resourcer
SRG Interesource| Placing People First
Clinical Recruitment Solutions
5th Flr, 16 St Helens Place
London EC3A 6DP
(w) 02075621795
Please Visit our new website : www.srginteresource.com
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