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Dear Allstat, I am currently recruiting for a global pharma company based in the Netherlands. We are seeking a Biostatistician for clinical projects/studies in all developmental phases and a Biostatistician specialising in early phase trials. Both positions are permanent roles. The Biostatistics Group provides statistical expertise to clinical development programmes in phases I through IV. We are looking for: Biostatistician for clinical projects/studies in all developmental phases You will work as a member of multi-disciplinary project and study teams providing statistical input from early study design discussions through to final study report, submission and beyond. Main responsiblities include contributing to clinical development plans and study designs, providing the statistical contribution to protocols and clinical study reports, writing analysis plans, programming inferential analyses in SAS, and providing sound statistical interpretation of results. You hold an MSc in statistics (or equivalent). Ideally you have several years relevant experience, but we are also interested to hear from bright newcomers. Responsibilities, grading and renumeration will be set appropriate to experience level. Biostatistician specialising in early phase trials Our Early Drug Development department focuses on early phase clinical studies in healthy volunteers or small, well defined patient populations as well as on later phase clinical pharmacology studies supporting registration. In addition the department is setting up a function for translational science, which will result in design and conduct of small target investigation studies as well as invention and implementation of biomarkers. This position will primarily support trials originating in this department. Main responsibilities similar to job description above, but focused on exploratory phase 0, 1-IIa trials. In addition you will look for opportunities to introduce innovative methodology, and optimise our statistical input to these trials. You will work across indications supporting/supervising the trials yourself, or acting as consultant to other biostatisticians for their projects. As a good communicator and problem solver, our colleagues in early drug development are eager to work with you. You hold an MSc in statistics (or equivalent) and have several years experience in clinical trials, preferably including early phase trials. Responsibilities, grading and renumeration will be set appropriate to experience level. Contact me with a copy of your CV in Word if you are interested in either position. Kind Regards, Martin Martin Grindrod Consultant ~ Biostatistics Division James Harvard Pharmaceutical Ltd T. 020 7922 7128 M. 07884 001 300 F. 020 7922 7101 E: [log in to unmask] W: www.jamesharvardpharma.com 25 - 27 Wootton Street : Waterloo : London : SE1 8TG For all our latest Stats and Programming vacancies please visit our website www.jamesharvardpharma.com Please consider the environment before printing this e-mail ______________________________________________________________________ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email ______________________________________________________________________