Summary:
This position, which reports to the Director of Analytical Services, will
provide support in the development, validation and utilization of
bioanalytical methods to support GLP and non GLP toxicology and PK studies.
Position or Core Responsibilities:
Working within a multi-disciplinary team of scientists, the candidate will
conduct HPLC and HPLC/MS bioanalytical method development, validation, and
analysis to support GLP and non GLP toxicology and PK studies. The position
will also lead the development, validation and testing of animal dosing
formulations. The incumbent will closely interact with preclinical
scientists conducting in vitro and in vivo pharmacology experiments to
discover and characterize novel molecules. Other responsibilities include
preparing reports and communicating accurate information in a timely manner.
An additional responsibility will be to contribute to the identification and
implementation of new technologies and processes that improve the group's
efficiency.
Essential Skills and Experience:
§ Hands-on experience with LC-MS/MS; including extensive experience in the
development of the LC-MS/MS and conventional HPLC bioanalytical methods for
support of GLP-compliant pre-clinical and clinical studies.
§ Experience supervision junior level scientists.
§ Through understanding of GLP regulations and extensive experience working
with QA.
§ Excellent verbal and written communication skills.
Education
PhD in chemistry or biological science and 5 years experience in
Pharmaceutical or Contract Research Organization.
If you have an interest in this or other opportunities, please send your
resume as a MS Word compatible file attached to email to the attention of
Basirah at RS&A. All correspondence is held in strict confidence.
--------------------------------------------------------------------------------
(Ms) Basirah Al'Basit
RS&A Scientific Search
Sedona, AZ 86341 USA
TEL: (928) 203-0074
EM: R...@sedona.net