Leading Biopharmaceutical
Contract Senior Statistical Programmers x 4
6 months Initially (12 months can be offered to exceptional candidates)
South East UK
£42 – £52 p/h
There are several long-term and financially rewarding contracts available with an industry leading Pharmaceutical client based in the south east – Work from home full-time 37.5 hours p/w
Expert Statistician
2 Year Long Contract
Germany
€75 – €90 p/h
The Biostatistician will be expected to provide input into the database design, prepare statistical analysis plans, and undertake extensive statistical analyses across phase II – III Diabetes trials
A busy and challening statistics department within a major pharmaceutical are looking for a senior statistician to join them on a contract basis.
Based in Surrey, with excellent transport links to and from London, this role would suit a statistician with 4 years expereince within a clinical setting who would like to make a move into contracting OR an existing contractor looking for a stable contract.
Job Summary:
Working for a major International Company on their long term projects you will provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase II – III clinical trials, ISS & ISE, primarily using SAS.
For a confidential consultation call Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com
Biostatistician x 3
Biopharmaceutical Client
Belgium
12 Months Rolling Contract
50 – 60 EURO P/H
To find out more details, please feel free to get in touch with Russell Gillam on +44 255 6665 OR send your CV to Russell.gillam@secpharma.com for immediate consideration
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com
Working in close collaboration with clinicians, statisticians and data managers, you will understanding clinical and statistical aspects of clinical trials.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@1st-pharmapeople.com
Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic submissions.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com
Working for this major pharmaceutical client within their statistics team, you will plan & lead study / project activities for data reporting.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com
Lead development, validation and maintenance of complex standard and study-specific CDM utilities, or suites of utilities – using SAS, and other technologies that are used for all global clinical trials, Phases I to IV.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com
CONTRACT: 2 x SAS Programmer
Phase I Oncology
6 month rolling contract
A leading medical device company with a track record of attracting and retaining some of the brightest talent in the industry currently ( due to expansion) has two new openings for a Clinical Scien More Details
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