Business Division Research Institute – Summit, NJ
Job Description:
This position serves as Study Director/Monitor for pre-clinical reproductive, developmental and general toxicology studies conducted in-house and/or at contract facilities.This position serves as Study Director/Monitor for pre-clinical reproductive, developmental and general toxicology studies conducted in-house and/or at contract facilities. · Study Director and/or Study Monitor for in-house and/or contracted preclinical toxicology and investigational studies. ¨ Design and conduct pre-clinical reproductive, developmental and general toxicology and investigational studies to meet specific departmental and Project team goals and regulatory requirements. ¨ As Study Director, accountable for all aspects of the conduct of the study, including protocol development, GLP and SOP compliance, evaluation and interpretation of results, and the writing and issuance of the final report. Responsible for interdepartmental and interdisciplinary collaboration in acquisition and evaluation of study materials, coordination of all study activities, and in interpretation and reporting of results. ¨ As Study Monitor, responsible for scientific monitoring (team and individual site visits and telephone liaison), consultation and advisement in study design, conduct, evaluation and reporting. Responsible for coordination of contract laboratory activities with other SPRI departments. ¨ The individual will serve as Study Director and provides scientific expertise and input for regulatory documents, and plans investigative programs. May represent Drug Safety and Metabolism on project team working groups and/or ad hoc committees providing scientific expertise.
Minimal education required for this job: Ph.D.
Skills:
· This position requires a Ph.D., or equivalent in Toxicology, Pharmacology and an understanding of teratology or reproductive biology.
· Previous Project Team and drug development experience desired, but not necessary.
· Candidate must also have excellent verbal and written communication and leadership skills including the ability to solve complex problems
· Experience in a GLP environment desired
As part of the Schering-Plough team, you'll benefit from strong leadership, a new vision and an empowering corporate culture…while enjoying competitive compensation and a progressive benefits package.
Schering-Plough is an Equal Opportunity Employer.
Employment Type Regular
Full-Time
Work Schedule Day
Requisition I.D. 24279BR
To apply, please visit:
http://www.schering-plough-jobs.com/job/SUMMIT-Principal-Scientist-(PhD)-Toxicology-Job-NJ-07901/517306/.
Schering-Plough is an Equal Opportunity Employer.
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