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Senior Study Director - Columbus, OH

Company: Ricerca Biosciences, LLC
Job type: full-time
Category: Research

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Job description



Responsibilities

BASIC SUMMARY:

Study Director for pilot and IND-enabling studies. Experience in chronic, investigative and carcinogenicity study designs. Responsible for the planning, conduct and successful reporting of assigned studies. Participate in report review and generation process. Develop new capabilities for Ricerca Biosciences. Communicate with Sponsors as required.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Participate in the proposal and bid development process

Serve as a key contact for sponsors

Participate in and coordinate all phases of the study planning process with Client Services and technical and laboratory support operations

Responsible for study design and generation of protocols

Interpret study data, write reports and draw conclusions

Develop and foster business relationships

Perform other duties as assigned

Qualifications

10 Years' experience as a Study Director in a CRO setting

PhD in Toxicology or Pharmacology or a related field. Ability to interact with multiple personality types and cultural backgrounds.

DABT preferred. Additional experience as a toxicologist, or related field in a governmental or industrial setting is preferable.

Working knowledge of Good Laboratory Practices regulations

Attention to detail and excellent interpersonal and communication skills


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