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Contenido proporcionado por Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.
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55: Ed Sequine: Health Pioneer Using Electronic Medical Records Solutions to Improve Clinical Trials

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Contenido proporcionado por Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

Edward Seguine is the CEO of Clinical Ink, a pioneer in the development of electronic source record solutions for clinical research. Prior to Clinical Ink, Mr. Seguine was the General Manager of Medidata’s Trial Planning product suite after serving as the CEO of Fast Track Systems before that company was acquired by Medidata.Mr. Seguine began his pharma career at Eli Lilly where he helped establish Lilly’s venture capital groups e.Lilly and Lilly Bioventures. Mr. Seguine has participated as an active board member and advisor for numerous start-up companies as well as CDISC. In addition, he has actively collaborated with leading academic institutions (Tufts CSDD, MIT, Duke) to develop, publish and present research into novel approaches to improving clinical development. Ed earned a BS in Finance from Brigham Young University, an MBA from Indiana University, and spent several years early in his career as the VP Finance of a start-up defense technology company. In this interview, Ed discusses the $7-10B industry of monitoring research sites for clinical trials, as well as the broader context and process of this dynamic and critical space including Meaningful Use.

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96 episodios

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Manage episode 308971995 series 3024395
Contenido proporcionado por Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Doug, Dr. Doug Elwood, Dr. Tom Elwood Presenting A Leading Podcast on Health, and Leadership with Amazing Featured Guests From Around Health o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

Edward Seguine is the CEO of Clinical Ink, a pioneer in the development of electronic source record solutions for clinical research. Prior to Clinical Ink, Mr. Seguine was the General Manager of Medidata’s Trial Planning product suite after serving as the CEO of Fast Track Systems before that company was acquired by Medidata.Mr. Seguine began his pharma career at Eli Lilly where he helped establish Lilly’s venture capital groups e.Lilly and Lilly Bioventures. Mr. Seguine has participated as an active board member and advisor for numerous start-up companies as well as CDISC. In addition, he has actively collaborated with leading academic institutions (Tufts CSDD, MIT, Duke) to develop, publish and present research into novel approaches to improving clinical development. Ed earned a BS in Finance from Brigham Young University, an MBA from Indiana University, and spent several years early in his career as the VP Finance of a start-up defense technology company. In this interview, Ed discusses the $7-10B industry of monitoring research sites for clinical trials, as well as the broader context and process of this dynamic and critical space including Meaningful Use.

  continue reading

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