Posted Date 2 days ago (12/17/2019 8:09 PM)
Job Number 2019-40187
Job Category Scientific Advanced
Position Type Full-Time
Job Overview We are looking to add a Study Director –
ADME/Metabolite ID to our Drug Metabolism team in Madison,
WI. The Study Director is responsible for managing the design,
conduct and reporting of studies to meet scientific, regulatory and
client requirements. The Study Director is the single point of
study control and has overall responsibility for the scientific,
technical and regulatory conduct of studies as well as for the
interpretation, documentation and reporting of results. Close and
regular liaison with the client is of primary importance.
The Study Director will demonstrate competence in directing
studies of intermediate complexity in design and scope. The
majority of studies undertaken will be non-GLP studies and routine
& more complex GLP, GCP or GMP studies.
With two state-of-the-art metabolism laboratories in Madison,
Wisconsin, and Harrogate, UK, Covance has helped hundreds of
pharmaceutical and biotechnology companies select compounds to
progress into development. Covance provides a comprehensive range
of ADME services to support drug discovery and development
At Covance, you can make a difference by helping to deliver
life-saving and life-enhancing medicines to people around the
world. Our commitment to this mission has resulted in Covance’s
impressive history of company stability and growth. We’ve achieved
these results by fostering a work environment that encourages,
develops and leverages our team’s capabilities.
Education/Qualifications PhD or equivalent preferred, or MSc/BSc
degree in an appropriate scientific discipline with some research
experience in drug development or similar field
Experience in a range of techniques/approaches relevant to the
department and/or unique expertise for a specific scientific
Knowledge of requirements for working within a GLP, GCP and GMP
(as appropriate) environment
Previous data interpretation and report writing experience
Working knowledge of software (eg, MS Word, Excel), specialty
applications (eg, Analyst, Sigmaplot, WinNonlin Phoenix), and
general IT skills
Experience Experience in the drug development process, knowledge
of regulatory requirements and the scientific techniques of
Metabolism studies required .
Experience of client management and technical expertise in the
relevant business line.
Fully competent in a feeder role for a study director with
skills and competencies in the relevant study types.
Covance, the drug development business of LabCorp, is recognized
as a leader in drug development because of our exceptional people.
At Covance, we embrace and celebrate the different strengths,
experiences and perspectives of our 20,000+ team members across the
globe. Our team is driven by an energizing purpose to improve
health and improve lives. Here, you can play a role in bringing new
scientific discoveries to life and make a difference in the lives
of millions. And, with our comprehensive service portfolio, you’ll
have the opportunity to explore diverse projects and unique career
paths across the drug development spectrum. Join us and discover
your extraordinary potential.
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