Statistician - 12 Months Contract - Netherlands For a confidential discussion Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com Job Summary: As a key member of the Clinical Trial Team, you will be responsible for all statistical aspects of the clinical study, such as statistical input into study design, the analysis and reporting plan, and the analysis ....click title for more details.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to james.carrera@secpharma.com Your primary responsibility will be to work as a statistician in the non-clinical research and development of new drugs, as well as in the quality and process control of pharmaceutical manufacturing. The position involves working closely with other statisticians, programme ....click title for more details.
For a confidential discussion, please get in touch with Russell Gillam on +44 255 6665 OR send your updated CV to russell.gillam@secpharma.com The Biostatistician will be expected to provide input into the database design, prepare statistical analysis plans, and undertake extensive statistical analyses. At the same time, as a Biostatistician, you will mentor and train colleagues, so your organi ....click title for more details.
For a confidential discussion, please get in touch with Russell Gillam on +44 207 255 6665. Alternatively you can e-mail your updated for immediate consideration to russell.gillam@secpharma.com Your primary responsibility will be the overseeing trial design and reporting. Preparing statistical aspects of development plans for new drug indications with minimum review. RESPONSIBILITIES: ....click title for more details.
CONTRACT: Statistician 12 Months Contract Netherlands For a confidential discussion Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com Job Summary: As a key member of the Clinical Trial Team, you will be responsible for all statistical aspects of the clinical study, such as statistical input into study design, the analysis and reporting plan, and th ....click title for more details.
For a confidential discussion Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com Job Summary: As a key member of the Clinical Trial Team, you will be responsible for all statistical aspects of the clinical study, such as statistical input into study design, the analysis and reporting plan, and the analysis and interpretation of results. CONTRACT: C ....click title for more details.
Senior Statistician (Expert level) - Based in Switzerland - CHF 130,000 -150,000 - Dependant on Experience For a confidential consultation call Louise Beka on 0044 (0) 207 255 6665 or email your CV to louise.beka@secpharma.com Job Summary: Our client is an international pharmaceutical company with offices around the world that is currently seeking a Senior Statistician at an expert level. T ....click title for more details.
Senior Statistician (Expert level) - Based in Switzerland - CHF 130,000 -150,000 - Dependant on Experience For a confidential consultation call Louise Beka on 0044 (0) 207 255 6665 or email your CV to louise.beka@secpharma.com Senior Statistician (Expert level) - Based in Switzerland - CHF 130,000 -150,000 – Dependant on Experience For a confidential consultation call Louise Beka ....click title for more details.
Permanent Senior/Expert Statistician - Permanent - Switzerland Permanent Senior/Expert Statistician - Switzerland Our client is an international pharmaceutical company with a global presence and actively working on Cardiovascular, Oncology, CNS and Respiratory studies. They are now looking for a permanent Senior Statistician to join their growing team based in Switzerland to work on various ....click title for more details.
For a confidential consultation call Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com Your primary responsibility will be the overseeing trial design and reporting. Preparing statistical aspects of development plans for new drug indications with minimum review. Act as Statistics representative for cross-functional teams and management review, including T ....click title for more details.
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