George Betts, MBA, CPM
3 SlideShares 10 Followers 3 Folgens
Personal Information
Unternehmen/Arbeitsplatz
Greater New York City Area United States
Beruf
Sr. Director, Head of Medical Affairs Operations - North America
Branche
Medical / Health Care / Pharmaceuticals
Webseite
%EE%82%A4https://www.linkedin.com/in/gbetts
Info
• Responsible for Medical Affairs Operations which includes the following functions: Clinical Operations, Biostatistics, Quality Operations, and Medical Information Management. • Lead strategic planning activities for Medical Affairs in North America including strategic input into product launch plans. • Oversee CME Grants and Investigator-Initiated Research programs, including GRC and MRC Committees. • Oversee operational and departmental budgeting, resource and financial management for Medical Affairs. • Provide leadership for the development and operational execution of both interventional and non-interventional late phase studies, including patient registry studies. •
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clinical trial operations investigator sponsored study investigator initiated research investigator sponsored studies iir compliance investigator initiated studies iits public relations iit investigator initiated study iirs decreasing cycle-time protocol development case study six sigma clinical study start-up process improvement clinical operations. monitoring clinical project management. patient enrollment clinical trial monitoring risk-based monitoring clinical operations study start-up clinical study
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(2)

Investigator initiated trials (ExL Conference April-2012)

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Monitoring Plan Template

www.datatrak.com • Vor 9 Jahren
Personal Information
Unternehmen/Arbeitsplatz
Greater New York City Area United States
Beruf
Sr. Director, Head of Medical Affairs Operations - North America
Branche
Medical / Health Care / Pharmaceuticals
Webseite
%EE%82%A4https://www.linkedin.com/in/gbetts
Info
• Responsible for Medical Affairs Operations which includes the following functions: Clinical Operations, Biostatistics, Quality Operations, and Medical Information Management. • Lead strategic planning activities for Medical Affairs in North America including strategic input into product launch plans. • Oversee CME Grants and Investigator-Initiated Research programs, including GRC and MRC Committees. • Oversee operational and departmental budgeting, resource and financial management for Medical Affairs. • Provide leadership for the development and operational execution of both interventional and non-interventional late phase studies, including patient registry studies. •
Tags
clinical trial operations investigator sponsored study investigator initiated research investigator sponsored studies iir compliance investigator initiated studies iits public relations iit investigator initiated study iirs decreasing cycle-time protocol development case study six sigma clinical study start-up process improvement clinical operations. monitoring clinical project management. patient enrollment clinical trial monitoring risk-based monitoring clinical operations study start-up clinical study
Mehr anzeigen