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Covance Associate Study Director in Greenfield, Indiana

Job Overview:

Come join a leader in drug development. We have an immediate opening for an Associate Study Director. This role is responsible for managing the design, conduct and reporting of in vivo Pharmacokinetic studies. 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 Associate Study Director will demonstrate competence in directing routine non-GLP PK screening studies.

Patients can't wait. Neither can we.

Education/Qualifications:

  • MS or equivalent/BSc degree in an appropriate scientific discipline with limited research experience in in a relevant field

  • MS with 1-3 years of related experience; orBS with 3-5 years of related experience

  • Relevant experience may be substituted for academic qualifications.

Experience:

  • Basic awareness of the drug development process, regulatory requirements and the scientific techniques of standard metabolism studies required.

  • Experience of client management and technical expertise in the relevant business line.

  • Experience in a feeder role for a study director with skills and competencies in some of the relevant study types.

  • At least 2 years at previous level

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.

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