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dc.contributor.advisorNelson Repenning and Brian Seed.en_US
dc.contributor.authorSmith, Peter J. A. (Peter John Anthony), 1959-en_US
dc.contributor.otherHarvard University--MIT Division of Health Sciences and Technology.en_US
dc.date.accessioned2005-09-27T17:11:06Z
dc.date.available2005-09-27T17:11:06Z
dc.date.copyright2004en_US
dc.date.issued2004en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/28588
dc.descriptionThesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology; and, (S.M.M.O.T.)--Massachusetts Institute of Technology, Sloan School of Management, Management of Technology Program, 2004.en_US
dc.descriptionIncludes bibliographical references (leaves 60-61).en_US
dc.description.abstractThe decline in Pharmaceutical R&D productivity has been attributed to high clinical failure rates suggesting that targets, leads and clinical candidates may be of lower quality in recent years. Senior R&D management generally believes that a greater integration of drug discovery and development will improve the selection and optimization of clinical candidates. I demonstrate the different nature of discovery and development with discovery tasks seen as more uncertain, having more reciprocal work flows and more under the control of management than development tasks. Discovery and development personnel have different characteristics and motivations, with discovery staff having greater creative skills and development staff greater planning skill. Following a congruence approach to organization design these differences imply that a complete merging of discovery and development functions would lead to poor fit between organizational design elements. This leaves an ongoing requirement for integrative systems which can preserve the important characteristic of discovery and development functions yet provide knowledge integration at key decision points to improve the quality of clinical candidates. A wide range of integrating mechanisms was found to be in use with an emphasis on cross functional teams. Information Technology was viewed as necessary infrastructure but not an important component of knowledge integration. No strong links were found between pipeline maturity and the integrative mechanism deployed. I speculate that company R&D performance could be better matched to internal and external circumstances by a more active approach to managing integrative systems. I propose a conceptual model of integrative systems to guide a more dynamic management approachen_US
dc.description.abstract(cont.) to organizational design of R&D and suggest further work to formalize the model through an agent based simulation.en_US
dc.description.statementofresponsibilityby Peter J.A. Smith.en_US
dc.format.extent69 leavesen_US
dc.format.extent2976003 bytes
dc.format.extent2982790 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectManagement of Technology Program.en_US
dc.subjectHarvard University--MIT Division of Health Sciences and Technology.en_US
dc.titleOrganizational design : the integration of pharmaceutical discovery and developmenten_US
dc.typeThesisen_US
dc.description.degreeS.M.M.O.T.en_US
dc.description.degreeS.M.en_US
dc.contributor.departmentManagement of Technology Program.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.contributor.departmentSloan School of Management
dc.identifier.oclc57490175en_US


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