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Covance Study Director in Greenfield, Indiana

Job Overview:

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.

We have a Study Director position open in our General Toxicology area at our site in Greenfield, IN.

This role:

  • Serves as the single point of control for safety assessment studies and being legally responsible for the study.

  • Learns overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results.

  • Is the main client contact and advisor for ongoing studies and must develop a full understanding of the Sponsor’s requirements.

What we’re looking for in you:

  • PhD in toxicology or related subject, DVM or equivalent degree is preferred.

  • Skilled in performing scientific presentations and preparing scientific publications.

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

Patients can’t wait. Neither can we.

Education/Qualifications:

PhD in toxicology or related subject, DVM or equivalent degree is preferred. BSc or equivalent or MSc required. Experience may be substituted for education.

Experience:

  • Zero to two years of related experience.

  • The job holder will have been fully competent at 111 grade, or have the equivalent skill set and have developed skills and competencies in the basic study types.

  • Skilled in performing scientific presentations and preparing scientific publications.

  • Experience may have been gained in study directing within the department in question or within a similar role external to Covance.

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

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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