Dear Allstat Members
Apologies for cross posting.
My client is a world leader in the research and development of products to protect and improve health and well-being. Their core businesses are in pharmaceuticals, consumer health, generics, eye-care, and animal health.
There are now several vacancies for Statistical and Programming staff at their HQ in Basel, Switzerland:
CP Senior Statistician
The CP Senior Statistician acts as project statistician for the assigned clinical pharmacology projects. He/she must interact globally with International Clinical Pharmacological Teams, Clinical Trial teams, Clinical Pharmacology, Marketing, DRA, Medical Data Management (MDM), and Statistical Programming (SP) as well as with CROs with respect to statistical activities contracted out.
Professional Requirements
In depth knowledge and expertise in statistics and its applications to clinical trials and their PK/PD parts. Solid knowledge of drug development process and HAs guidelines especially in regard to CP and PK. Background medical and pharmacokinetics knowledge. Good working knowledge of statistical software packages. Good data exploration and modelling skills. Very good communication and presentation skills. Ability to give guidance to trial statisticians. Good team worker. Good business ethics. Fluent English, oral and written.
TA Statistician
The TA Statistician is responsible for all statistical tasks of individual clinical trials. He/she must work in conjunction with the project statistician and interact with members of the Clinical Trial Team and the International Clinical Team, Medical Data Management (MDM), and Medical Data Structure and Programming (MDSP) as well as with CROs with respect to statistical activities contracted out. He/she may take on project level tasks of a Project Statistician initially under the supervision of a Senior Statistician/Group Head but with increasing autonomy and accountability.
Professional Requirements
Good level of knowledge in Statistics and its applications to clinical trials. Good knowledge of drug development and HAs guidelines. Background medical knowledge. In depth knowledge of statistical software packages. Good communication and presentation skills. Good team worker. Fluent English, oral and written.
Clinical SAS Programmer
To provides analysis datasets, pooled datasets, listings, summaries, figures and tables for phase I-IV clinical trials and for ISS and ISE according to CDP specifications.
Professional Requirements
Knowledge/experience in SAS software. Knowledge of global clinical trial practices, procedures, methodologies. Excellent verbal and written communication skills. Excellent presentation, organizational, interpersonal and diplomacy skills. Continuous improvement mentality and attention to detail. Intermediate knowledge of office tools.
For full job specifications and details of other positions please attach your CV by return of mail.
Kind regards,
Nik
Nik East
Director
Tel: 44 (0) 161 448 9105
Mob: 44 (0) 7985 483211
Mail: [log in to unmask]
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This message may contain confidential information & is intended only for the individual named.
Any opinions expressed here are those of the author and do not necessarily represent the views of TotalPharm Ltd:
Registered in England 4728249
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