Jean GARUTTI pact at
Thu Dec 12 11:27:35 EST 1996

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A dynamic and pioneering company, located just outside Paris, is
seeking  an autonomous, disciplined individual to  take on the
responsibility of being the No2  in the department.  Interfacing with
other departments and dealing with MD and local agencies this individual
will report to the VP Worldwide Regulatory Affairs and the President and
be based at the Company’s corporate HQ. 

You are  in your  late twenties to early thirties.

You are medically qualified  or have an equivalent scientific
qualification with exposure to pharmacology/ toxicology.

You have 3-4 years experience within an international pharmaceutical
environment dealing with adverse drug reactions.

Your background includes: classification of  ADR, preparing reports
according to CIOMs; clinical research exposure as well as regulatory
affairs and data management knowledge.

You are fluent in English and possibly another European language.  Of an
extrovert nature, you can integrate into and work well within a
multi-disciplinary, multi-cultural team.  You are geographically
flexible - as travelling is an important aspect of this role.

For more information please contact Alexia on: pact at

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