Study Director – Developmental and Reproductive Toxicology (DART), Greenfield, Indiana

We currently have a great opportunity for a STUDY DIRECTOR – DEVELOPMENTAL AND REPRODUCTIVE TOXICOLOGY (DART) at our Greenfield, IN facility.  Covance’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide.  Be a part of this life-saving work.

 

This role:

  • Serves as the DART Study Director for DART Toxicology Studies, including Embryo-fetal Development, Fertility, Pre-/Postnatal and Juvenile Toxicology Studies as described in the GLPs.
  • Has overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results.
  • Stays current with DART study designs and techniques and suggest ideas for technical development as appropriate
  • Is considered a subject matter expert in one or more of the following: fetal pathology, endocrinology, behavioral toxicity/neurotoxicity, juvenile toxicity
  • Reviews and confirms external, visceral and skeletal fetal abnormalities
  • Trains on providing expert consultations to clients on customized DART study designs and study timings according to drug development needs

 

 What we’re looking for in you:

  • PhD in toxicology or related subject, DVM or equivalent degree is preferred.
  • One to five years of related experience.
  • Skilled in performing scientific presentations and preparing scientific publications.
  • Experience of client management and technical expertise in the relevant business line.

 

There is no better time to join us!

 

If interested in setting up a time at the Teratology meeting  to learn more about this position, contact me at tricia.cullen@covance.com.  Or apply on-line to  http://jobsearch.covance.com/18797-jobs.

 

Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

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