Study Director I

Why Wait? Our passion is unmistakable! Have you ever wished you could be as excited about your career as you once were? Or wanted to take your career to the next level without needing to leave your organization for professional growth? Welcome to Covance.



As a billion dollar company with widespread global reach, Covance's ability to offer integrated drug development services is unsurpassed. Our employees are passionate about delivering excellent customer service and unfaltering science. If you are looking to re-energize your career, Covance is the place to be.


Nonclinical testing is conducted throughout all phases of drug development and, when done well, can maximize the chances of success in the clinical phases. The goal of our nonclinical studies is to determine which compounds have the greatest probability of success, and to build a solid scientific foundation that spans all stages of clinical development. Covance offers comprehensive services in all areas of nonclinical drug development including toxicology, pharmacology, metabolism, bioanalysis, pharmaceutical analysis and biosafety testing in support of nonclinical drug development.



Covance Labs North America is seeking a Toxicology Study Director for its Madison, WI facility. As a Study Director, you will maintain overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results. Specifically, you will:




Coordinate the efforts of the study team.

Learn to develop protocols and ensure that the protocol, including any changes, is approved and is in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines.

Learn to review cost estimates to ensure that all protocol/amendment driven workscope specifications have been included in the price estimation.

Understand financial status of ongoing studies.

Monitor progress and status of assigned studies. Ensure that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified.

Direct preparation of reports, ensure compliance with protocol and regulatory requirements, and submit them to the client.

Participate in and may host client visits.

Qualifications

PhD, DVM, or equivalent degree plus 0-2 years of experience. Experience may be substituted for education.

Skilled in performing scientific presentations and preparing scientific publications.

Post-doctoral experience or post-graduate industrial experience desired.





At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. Covance is well-positioned for continued growth!


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