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Study Director - ADME/Metabolite ID

Company: Covance, Inc.
Location: Madison
Posted on: September 14, 2020

Job Description:

Posted Date 2 days ago (12/17/2019 8:09 PM)

Job Number 2019-40187

Job Category Scientific Advanced

Position Type Full-Time

Telecommute No

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 programs.

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 service

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.

From FORTUNE. (c)2019 Fortune Media IP Limited. All rights reserved. Used under license.FORTUNE and The World's Most Admired Companies are registered trademarks of Fortune MediaIP Limited and are used under license. FORTUNE and Fortune Media IP Limited are not affiliatedwith, and do not endorse products of, Laboratory Corporation of America Holdings.

Keywords: Covance, Inc., Madison , Study Director - ADME/Metabolite ID, Other , Madison, Wisconsin

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