Pre-Clinical Research Scientist

Location
Switzerland
Salary
Negotiable
Posted
Feb 03, 2012
Closes
Mar 03, 2012
Ref
717661
Contact
Sergio Carito
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Full Time
My Client, a world leading pharmaceutical company, is looking for a talented individual to work as Pre-Clinical Research Scientist. The professional we are looking for has to be fluent in German and English.

Acting as study director and study personnel for non-clinical studies (GLP-studies according to GLPV SR 813.112.1 and non-GLP-studies), You will create study protocols and reports for GLP- and non-GLP-studies, according to GLP-Guidelines. You will perform animal studies supporting the implementation of new in vivo (disease) models. You will also cooperate with department for chemical research and development for test item delivery, formulation and application and with Biology Group for conduction of animal?s studies and provision of test material. Other important responsibilities are the cooperation with QA-department for GLP-compliance and the support to internal audits.

With a Degree in life sciences, pharmacology or veterinary pathology and training for conducting animal experiments (LTK-Module 1 or 2), the right candidate is experienced to work with rodents (drug application techniques, sampling of specimens like blood, organs or cells) and with different animal models (inflammation, oncology, nephrology would be an asset). This role requires experience with different analytical methods, preferably haematological, biochemical and immunological methods (FACS analysis, histology) and in-depth knowledge of appropriate statistical methods for data analysis, GLP regulation.

My Client can offer an interesting and challenging function in a young, motivated team as well as the advantages of a modern company with excellent social benefits.

To apply, forward your CV to Sergio.carito@secpharma.com
Call Sergio Carito on + 44(0)207 255 66 65 for further information and a confidential discussion of this opportunity.

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