Reference: VETSAF11 Date of the offer: 14/12/2011 Expiration: 30/06/2012
Description:
Unlimited term contract
Location: Evreux (France)
Fixed Salary : To be defined according to skills and experience
Essential duties and responsibilities:
Act as a Study Director for Safety Pharmacology Studies within a GLP environment
Establish study protocols in compliance with relevant guidelines and taking into account animal welfare. Interpret, evaluate and document the obtained data. Write study reports.
Maintain close and regular client contacts : consulting
Represent CIT in a professional manner at all time (client visits, national and international congresses)
Act as a veterinarian
Knowledge skills and abilities:
General expertise in pharmacology and special focus on cardiovascular, central nervous system and respiratory physiology and pharmacology
General expertise in experimental surgery
Ability to develop and validate new challenging scientific techniques
Ability to focus on the quality of the work and process improvement
Good communication skills with internal scientists and clients
Special focus on productivity
Team worker with ability to define and deal with priorities
High degree of professionalism, scientific rigour and understanding with consistent attention to details and results
Ability to build and maintain strategic working relationship, with tenacious approach (confident and persuasive manners) but a positive attitude and good ability to change (flexibility)
Qualifications and requirements:
Veterinary Diploma
Strong experience in experimental surgery at least 2 years
Writing and speaking fluently English
Strong organization skills and ability to resolve scientific challenges
Good knowledge of GLP regulations
Good knowledge of pharmaceutical and biologic development
Publication record is an advantage
Send resume/CV and letter to : Mrs Mélinda LE BRETON, Ref VETSAF11