Consulting for the Life Sciences since 1998      |     caymanscientific.com
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    • Clinical Document Management: A Trial-by-Trial Approach to Compliance™
    • Clinical Trial Project Management for Phase 1 to Phase 4: Best Practices™
    • Clinical Trial Data Analysis: Audits, Vendor Selection and Project Management
    • Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™
    • Project Management in Clinical Development
    • Selecting and Managing CROs
    • Writing Effective Standard Operating Procedures and Other Process Documents
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Two Case Studies


1:  From CRO to TRO

A Japanese pharmaceutical company wanted to move their organization from a "CRO-type" service provider to a translational research organization. CSC worked specifically on transitioning the Clinical Operations group into a Project Management Office and, with training and organizational development work, ensured that staff was ready to support the new organization.

CSC supported the work of developing the overall transition strategy for the company and the development of a stage-gate process to identify and move compounds into and through the portfolio.
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2:  A Bay Area Malaria Symposium

A new non-profit working on the eradication of malaria needed help with managing their annual scientific symposium. CSC brought together volunteers, sponsors and a process that enabled the organization to hold a full-day symposium complete with keynote speakers, presentations and poster sessions. The event has, over the past three years, become one of the premier events for innovative malaria research in the San Francisco Bay Area.


CONSULTING FOR THE LIFE SCIENCES SINCE 1998


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