董事介绍
注:董事持股数取自最新公司公告
| 姓名 | 性别 | 职位 | 年龄 | 薪酬 | 持股数(万股) | 截止日期 |
|---|---|---|---|---|---|---|
| Lonnel Coats | 男 | Director | 53 | 36.83万美元 | 未持股 | 2018-04-15 |
| Jeffrey W. Albers | 男 | President,Chief Executive Officer and Director | 46 | 493.84万美元 | 未持股 | 2018-04-15 |
| George D. Demetri | 男 | Director | 61 | 36.98万美元 | 未持股 | 2018-04-15 |
| Nicholas Lydon | 男 | Director | 61 | 39.08万美元 | 未持股 | 2018-04-15 |
| Lynn Seely | 女 | Director | 59 | 36.73万美元 | 未持股 | 2018-04-15 |
| Charles A. Rowland, Jr. | 男 | Director | 59 | 38.23万美元 | 未持股 | 2018-04-15 |
| Alexis Borisy | 男 | Director | 46 | 36.23万美元 | 未持股 | 2018-04-15 |
| Daniel S. Lynch | 男 | Chairman and Director | 60 | 38.73万美元 | 未持股 | 2018-04-15 |
| Daniel S. Lynch | 男 | Chairman and Director | 60 | 未披露 | 未持股 | 2018-04-15 |
| Mark Goldberg | 男 | Director | 63 | 37.48万美元 | 未持股 | 2018-04-15 |
高管介绍
注:高管持股数取自最新公司公告
| 姓名 | 性别 | 职位 | 年龄 | 薪酬 | 持股数(万股) | 截止日期 |
|---|---|---|---|---|---|---|
| Jeffrey W. Albers | 男 | President,Chief Executive Officer and Director | 46 | 493.84万美元 | 未持股 | 2018-04-15 |
| Anthony L. Boral | 男 | Chief Medical Officer | 55 | 166.40万美元 | 未持股 | 2018-04-15 |
| Kathryn Haviland | 女 | Chief Business Officer | 42 | 146.47万美元 | 未持股 | 2018-04-15 |
| Michael Landsittel | 男 | Vice President, Finance | 46 | 84.29万美元 | 未持股 | 2018-04-15 |
| Marion Dorsch | 女 | Chief Scientific Officer | 53 | 288.23万美元 | 未持股 | 2018-04-15 |
| Tracey L. McCain | 女 | Chief Legal and Compliance Officer | 50 | 212.42万美元 | 未持股 | 2018-04-15 |
| Christopher K. Murray | -- | Senior Vice President, Technical Operations | 55 | 353.93万美元 | 未持股 | 2018-04-15 |
董事简历
中英对照 |  中文 |  英文- Lonnel Coats
-
Lonnel Coats,2014年7月以来,一直担任本公司的总裁、首席执行官、董事。1996年至2014年6月,他在Eisai Inc. 、Eisai Corporation of North America担任过一系列领导职务;最后的是首席执行官,2010年至2014年6月;2004-2010,担任其总裁、首席运营官。加入Eisai之前,他在Janssen Pharmaceuticals, Inc工作了8年,担任过各种管理、销售职务,这是Johnson & Johnson的分部。他在Oakland University获得公共管理学士学位。
Lonnel Coats,has been Lexicon Pharmaceuticals, Inc. chief executive officer and a director since July 2014. Mr. Coats previously served in a series of executive leadership positions at Eisai Inc. and Eisai Corporation of North America, where he worked for 18 years before joining Lexicon Pharmaceuticals, Inc. company, most recently as chief executive officer from 2010 to 2014. Prior to joining Eisai, Mr. Coats spent eight years with Janssen Pharmaceuticals, Inc., a division of Johnson & Johnson, where he held a variety of management and sales positions. Mr. Coats serves as a director of Blueprint Medicines Corporation and Verve Therapeutics, Inc., and holds a B.S. from Oakland University. - Lonnel Coats,2014年7月以来,一直担任本公司的总裁、首席执行官、董事。1996年至2014年6月,他在Eisai Inc. 、Eisai Corporation of North America担任过一系列领导职务;最后的是首席执行官,2010年至2014年6月;2004-2010,担任其总裁、首席运营官。加入Eisai之前,他在Janssen Pharmaceuticals, Inc工作了8年,担任过各种管理、销售职务,这是Johnson & Johnson的分部。他在Oakland University获得公共管理学士学位。
- Lonnel Coats,has been Lexicon Pharmaceuticals, Inc. chief executive officer and a director since July 2014. Mr. Coats previously served in a series of executive leadership positions at Eisai Inc. and Eisai Corporation of North America, where he worked for 18 years before joining Lexicon Pharmaceuticals, Inc. company, most recently as chief executive officer from 2010 to 2014. Prior to joining Eisai, Mr. Coats spent eight years with Janssen Pharmaceuticals, Inc., a division of Johnson & Johnson, where he held a variety of management and sales positions. Mr. Coats serves as a director of Blueprint Medicines Corporation and Verve Therapeutics, Inc., and holds a B.S. from Oakland University.
- Jeffrey W. Albers
-
Jeffrey W. Albers自2014年7月起一直担任公司首席执行官及总裁和我们的董事会成员。Albers先生生物制药行业担任近十年的领导职务。2012年1月至2014年4月,加入我们之前,他是Algeta ASA或Algeta U.S。(一家挪威的生物制药公司)美国分公司的总裁,在那里他负责商业和商务职务。在Algeta U.S.,Albers先生负责在美国推出治疗转移性阉割性前列腺癌的镭223。在Algeta U.S。之前,2005年7月至2011年11月,Albers先生任职于Genzyme公司(或Genzyme)。Genzyme是一个生物技术公司,现在是Sanofi S.A.的全资子公司,最近担任美国血液学和肿瘤药品事业部的副总裁。Albers先生获得Indiana University学士学位和Indiana University, Georgetown University法学博士学位。
Jeffrey W. Albers has served as our president and chief executive officer and a member of our board of directors since July 2014. In addition, Mr. Albers currently serves on the board of directors of Magenta Therapeutics, Inc., a privately held biopharmaceutical company, and on the board of directors of the New England Division of the American Cancer Society. Prior to joining us, from January 2012 to April 2014 he was president of Algeta ASA, or Algeta, a Norwegian biopharmaceutical company, where he oversaw the commercial and business functions. At Algeta, Mr. Albers was responsible for the U.S. launch of Radium‑223 in metastatic castrate resistant prostate cancer. Prior to Algeta, from July 2005 to November 2011 Mr. Albers was at Genzyme Corporation, or Genzyme, a biotechnology company that is now a wholly-owned subsidiary of Sanofi S.A., most recently as vice president of the U.S. hematology and oncology business unit. Mr. Albers received a B.S. from Indiana University and an M.B.A. and a J.D. from Georgetown University. - Jeffrey W. Albers自2014年7月起一直担任公司首席执行官及总裁和我们的董事会成员。Albers先生生物制药行业担任近十年的领导职务。2012年1月至2014年4月,加入我们之前,他是Algeta ASA或Algeta U.S。(一家挪威的生物制药公司)美国分公司的总裁,在那里他负责商业和商务职务。在Algeta U.S.,Albers先生负责在美国推出治疗转移性阉割性前列腺癌的镭223。在Algeta U.S。之前,2005年7月至2011年11月,Albers先生任职于Genzyme公司(或Genzyme)。Genzyme是一个生物技术公司,现在是Sanofi S.A.的全资子公司,最近担任美国血液学和肿瘤药品事业部的副总裁。Albers先生获得Indiana University学士学位和Indiana University, Georgetown University法学博士学位。
- Jeffrey W. Albers has served as our president and chief executive officer and a member of our board of directors since July 2014. In addition, Mr. Albers currently serves on the board of directors of Magenta Therapeutics, Inc., a privately held biopharmaceutical company, and on the board of directors of the New England Division of the American Cancer Society. Prior to joining us, from January 2012 to April 2014 he was president of Algeta ASA, or Algeta, a Norwegian biopharmaceutical company, where he oversaw the commercial and business functions. At Algeta, Mr. Albers was responsible for the U.S. launch of Radium‑223 in metastatic castrate resistant prostate cancer. Prior to Algeta, from July 2005 to November 2011 Mr. Albers was at Genzyme Corporation, or Genzyme, a biotechnology company that is now a wholly-owned subsidiary of Sanofi S.A., most recently as vice president of the U.S. hematology and oncology business unit. Mr. Albers received a B.S. from Indiana University and an M.B.A. and a J.D. from Georgetown University.
- George D. Demetri
-
George D. Demetri,2014年12月以来,他一直担任我们董事会的成员。1988年以来,他曾一直担任Harvard Medical School的医学教授,以及达那-法伯癌症研究所(the Dana-Farber Cancer Institute)和Harvard Medical School的学术医疗肿瘤学家。他拥有研究和临床投资专注于实体肿瘤药物开发,特别强调分子定义的肉瘤,如胃肠道间质肿瘤。他曾贡献于治疗肉瘤等恶性肿瘤的一些新药的开发,包括伊马替尼、舒尼替尼、达沙替尼、曲贝替定、维罗非尼、依维莫司、帕唑帕尼、瑞格非尼。他担任the Sarcoma Foundation of America,以及一些科学和编辑顾问委员会的医学顾问委员会的主席。他投资于互联网的病人支持,也曾任职于ASCO's CancerNet、CancerCommons.org的医学顾问委员会。他持有Harvard College的生物化学学士学位,以及Stanford University School of Medicine的医学博士学位。
George D. Demetri, M.D. has served as a member of our board of directors since November 2017. Since 1986 Dr. Demetri has served as a Professor of Medicine at Harvard Medical School and as a Physician-Scientist Faculty Member at the Dana-Farber Cancer Institute. Dr. Demetri leads a multidisciplinary team at the Dana-Farber/Harvard Cancer Center focused on developing novel therapies for solid tumors, with an emphasis on sarcomas. Dr. Demetri’s research and clinical interests have centered on mechanism-based drug development for solid tumors, and he is a world-renowned expert in the clinical translation of innovative treatment strategies for cancer. Dr. Demetri has contributed to the development of numerous approved therapies, including Gleevec imatinib, Sutent (sunitinib), Stivarga (regorafenib), Zelboraf (vemurafenib) and Votrient (pazopanib), as well as other new targeted therapies in development. Dr. Demetri also currently serves on the board of directors and scientific advisory board of Blueprint Medicines Corporation. Dr. Demetri holds an M.D. from Stanford University School of Medicine and an A.B. from Harvard College. - George D. Demetri,2014年12月以来,他一直担任我们董事会的成员。1988年以来,他曾一直担任Harvard Medical School的医学教授,以及达那-法伯癌症研究所(the Dana-Farber Cancer Institute)和Harvard Medical School的学术医疗肿瘤学家。他拥有研究和临床投资专注于实体肿瘤药物开发,特别强调分子定义的肉瘤,如胃肠道间质肿瘤。他曾贡献于治疗肉瘤等恶性肿瘤的一些新药的开发,包括伊马替尼、舒尼替尼、达沙替尼、曲贝替定、维罗非尼、依维莫司、帕唑帕尼、瑞格非尼。他担任the Sarcoma Foundation of America,以及一些科学和编辑顾问委员会的医学顾问委员会的主席。他投资于互联网的病人支持,也曾任职于ASCO's CancerNet、CancerCommons.org的医学顾问委员会。他持有Harvard College的生物化学学士学位,以及Stanford University School of Medicine的医学博士学位。
- George D. Demetri, M.D. has served as a member of our board of directors since November 2017. Since 1986 Dr. Demetri has served as a Professor of Medicine at Harvard Medical School and as a Physician-Scientist Faculty Member at the Dana-Farber Cancer Institute. Dr. Demetri leads a multidisciplinary team at the Dana-Farber/Harvard Cancer Center focused on developing novel therapies for solid tumors, with an emphasis on sarcomas. Dr. Demetri’s research and clinical interests have centered on mechanism-based drug development for solid tumors, and he is a world-renowned expert in the clinical translation of innovative treatment strategies for cancer. Dr. Demetri has contributed to the development of numerous approved therapies, including Gleevec imatinib, Sutent (sunitinib), Stivarga (regorafenib), Zelboraf (vemurafenib) and Votrient (pazopanib), as well as other new targeted therapies in development. Dr. Demetri also currently serves on the board of directors and scientific advisory board of Blueprint Medicines Corporation. Dr. Demetri holds an M.D. from Stanford University School of Medicine and an A.B. from Harvard College.
- Nicholas Lydon
-
Nicholas Lydon,2011年4月以来,他一直担任我们董事会的成员。他是Blueprint Medicines公司的科学创始人。2006年以来,他曾一直担任AnaptysBio公司(他共同创立的公司)的科学顾问和董事会成员。从2003年到2011年,他曾一直担任Ambit Biosciences公司(生物制药公司)的科学顾问和董事会成员。从2000年到2002年,他曾担任Amgen公司的副总裁,负责小分子药物发现。1997年加入Amgen公司之前,他曾创立Kinetix Pharmaceuticals公司(Kinetix公司,一个生物科技公司,专注于选择性蛋白激酶抑制剂的发现和开发,于2000年被Amgen公司收购),也曾担任其首席执行官,并任职于其董事会。他持有英国利兹大学(The University of Leeds)的生物化学和动物学学士学位,并持有苏格兰邓迪大学医学科学研究所(the Medical Sciences Institute, University of Dundee, Scotland)的生物化学博士学位。
Nicholas Lydon, Ph.D. is a scientific founder of Blueprint Medicines and has served as a member of our board of directors since April 2011. Since 2006 Dr. Lydon has served as a scientific advisor and member of the board of directors of AnaptysBio Inc., a company he co-founded. In addition, Dr. Lydon currently serves on the board of directors of Staurus Biopharma, LLC, a privately held biopharmaceutical company that he co-founded. From 2003 to 2009 Dr. Lydon served as a scientific advisor and member of the board of directors of Ambit Biosciences Corp., a biopharmaceutical company. From 2000 to 2002 Dr. Lydon served as vice president, small molecule drug discovery, at Amgen, Inc., or Amgen. Prior to joining Amgen, in 1997 Dr. Lydon founded Kinetix Pharmaceuticals, Inc., or Kinetix, a biotechnology company focused on the discovery and development of selective protein kinase inhibitors, which was acquired by Amgen in 2000 and served as Kinetix’s chief executive officer and member of its board of directors. Prior to founding Kinetix, Dr. Lydon worked for Ciba-Giegy AG now Novartis AG where he was responsible for the tyrosine protein kinase program, including the discovery and preclinical development of imatinib. Dr. Lydon received a B.S. in biochemistry and zoology from the University of Leeds, England, and received a Ph.D. in biochemistry from the Medical Sciences Institute, University of Dundee, Scotland. - Nicholas Lydon,2011年4月以来,他一直担任我们董事会的成员。他是Blueprint Medicines公司的科学创始人。2006年以来,他曾一直担任AnaptysBio公司(他共同创立的公司)的科学顾问和董事会成员。从2003年到2011年,他曾一直担任Ambit Biosciences公司(生物制药公司)的科学顾问和董事会成员。从2000年到2002年,他曾担任Amgen公司的副总裁,负责小分子药物发现。1997年加入Amgen公司之前,他曾创立Kinetix Pharmaceuticals公司(Kinetix公司,一个生物科技公司,专注于选择性蛋白激酶抑制剂的发现和开发,于2000年被Amgen公司收购),也曾担任其首席执行官,并任职于其董事会。他持有英国利兹大学(The University of Leeds)的生物化学和动物学学士学位,并持有苏格兰邓迪大学医学科学研究所(the Medical Sciences Institute, University of Dundee, Scotland)的生物化学博士学位。
- Nicholas Lydon, Ph.D. is a scientific founder of Blueprint Medicines and has served as a member of our board of directors since April 2011. Since 2006 Dr. Lydon has served as a scientific advisor and member of the board of directors of AnaptysBio Inc., a company he co-founded. In addition, Dr. Lydon currently serves on the board of directors of Staurus Biopharma, LLC, a privately held biopharmaceutical company that he co-founded. From 2003 to 2009 Dr. Lydon served as a scientific advisor and member of the board of directors of Ambit Biosciences Corp., a biopharmaceutical company. From 2000 to 2002 Dr. Lydon served as vice president, small molecule drug discovery, at Amgen, Inc., or Amgen. Prior to joining Amgen, in 1997 Dr. Lydon founded Kinetix Pharmaceuticals, Inc., or Kinetix, a biotechnology company focused on the discovery and development of selective protein kinase inhibitors, which was acquired by Amgen in 2000 and served as Kinetix’s chief executive officer and member of its board of directors. Prior to founding Kinetix, Dr. Lydon worked for Ciba-Giegy AG now Novartis AG where he was responsible for the tyrosine protein kinase program, including the discovery and preclinical development of imatinib. Dr. Lydon received a B.S. in biochemistry and zoology from the University of Leeds, England, and received a Ph.D. in biochemistry from the Medical Sciences Institute, University of Dundee, Scotland.
- Lynn Seely
-
Lynn Seely自2021年5月起担任Lyell Immunopharma, Inc.的董事会成员。Lynn Seely,从2002年9月至2005年3月,她担任前身为Corgentech Inc.的生物制药公司Anesiva, Inc.的临床发展副总裁。从1996年至2000年,她担任一家生物科技公司Chiron Corporation的临床发展副董事。在2000到2001年间,她担任私有医疗设备公司ProDuct Health, Inc.的临床发展副总裁。随后在2001年至2002年,她担任医疗设备公司Cytyc Corporation的子公司Cytyc Health Corporation的临床发展副总裁,同时对Cytyc Corporation并购 ProDuct Health, Inc.过渡事宜提供帮助。她在俄克拉荷马大学医学院(University of Oklahoma College of Medicine)获得硕士学位并于Yale-New Haven Hospital内科完成高级专科住院实习。Seely博士从俄克拉何马大学医学院获得医学博士学位,并在俄克拉何马大学获得新闻学士学位。Seely博士完成了她的居留,并担任耶鲁纽黑文医院内科住院医师,完成了她在圣地亚哥加利福尼亚大学的内分泌和代谢研究。
Lynn Seely has served as a member of our board of directors since May 2021. Dr. Seely currently serves as a member of the board of directors of Blueprint Medicines Corp., a publicly-traded pharmaceutical company. From June 2016 to January 2021 Dr. Seely served as President, Chief Executive Officer and a member of the board of directors of Myovant Sciences, a biotechnology company. From March 2005 to October 2015 Dr. Seely served as Senior Vice President and Chief Medical Officer of Medivation, a biotechnology company. Dr. Seely received an M.D. from the University of Oklahoma College of Medicine and a B.A. in Journalism from the University of Oklahoma. Dr. Seely completed her residency and served as chief resident in internal medicine at Yale-New Haven Hospital, and she completed her fellowship in endocrinology and metabolism at the University of California, San Diego. - Lynn Seely自2021年5月起担任Lyell Immunopharma, Inc.的董事会成员。Lynn Seely,从2002年9月至2005年3月,她担任前身为Corgentech Inc.的生物制药公司Anesiva, Inc.的临床发展副总裁。从1996年至2000年,她担任一家生物科技公司Chiron Corporation的临床发展副董事。在2000到2001年间,她担任私有医疗设备公司ProDuct Health, Inc.的临床发展副总裁。随后在2001年至2002年,她担任医疗设备公司Cytyc Corporation的子公司Cytyc Health Corporation的临床发展副总裁,同时对Cytyc Corporation并购 ProDuct Health, Inc.过渡事宜提供帮助。她在俄克拉荷马大学医学院(University of Oklahoma College of Medicine)获得硕士学位并于Yale-New Haven Hospital内科完成高级专科住院实习。Seely博士从俄克拉何马大学医学院获得医学博士学位,并在俄克拉何马大学获得新闻学士学位。Seely博士完成了她的居留,并担任耶鲁纽黑文医院内科住院医师,完成了她在圣地亚哥加利福尼亚大学的内分泌和代谢研究。
- Lynn Seely has served as a member of our board of directors since May 2021. Dr. Seely currently serves as a member of the board of directors of Blueprint Medicines Corp., a publicly-traded pharmaceutical company. From June 2016 to January 2021 Dr. Seely served as President, Chief Executive Officer and a member of the board of directors of Myovant Sciences, a biotechnology company. From March 2005 to October 2015 Dr. Seely served as Senior Vice President and Chief Medical Officer of Medivation, a biotechnology company. Dr. Seely received an M.D. from the University of Oklahoma College of Medicine and a B.A. in Journalism from the University of Oklahoma. Dr. Seely completed her residency and served as chief resident in internal medicine at Yale-New Haven Hospital, and she completed her fellowship in endocrinology and metabolism at the University of California, San Diego.
- Charles A. Rowland, Jr.
-
Charles A. Rowland, Jr.(小),2014年9月起成为公司董事会成员。目前他担任战略顾问。2008年10月起到2014年1月公司被Shire plc收购,他担任国际制药公司ViroPharma Incorporated的副总裁兼首席财务官。加入ViroPharma前,2006年12月至2008年9月,他曾是Endo Pharmaceuticals Inc.的执行副总裁、首席财务官和临时联合首席执行官,该公司是一家疼痛管理专业制药公司。2004年至2006年,他担任国际制药公司Biovail Corporation的高级副总裁兼首席财务官。之前,他也曾在Breakaway Technologies公司、Pharmacia Corporation、Novartis AG 和Bristol-Myers Squibb Co。任职。目前他任职于BIND Therapeutics公司和Aurina Pharmaceuticals公司的董事会。2013年至2014年8月公司被默克(Merck & Co., Inc.)收购期间,他任职于Idenix Pharmaceuticals公司的董事会。他同时也是费城Financial Executives International的董事会成员。他取得了圣约瑟夫大学(St. Joseph's University)会计学士和罗格斯大学(Rutgers University)工商管理硕士学位。
Charles A. Rowland, Jr. has served on our board of directors since June 23 2017. Mr. Rowland previously served on the supervisory board of Nabriva Austria from January 2015 until the Redomiciliation. Mr. Rowland served as chief executive officer of Aurinia Pharmaceuticals Inc. from April 2016 to January 2017. Mr. Rowland previously served as vice president and chief financial officer of ViroPharma Incorporated from 2008 until it was acquired by Shire plc in 2014. Prior to joining ViroPharma, Mr. Rowland served as executive vice president and chief financial officer, as well as interim co-chief executive officer, for Endo Pharmaceuticals Inc. from 2006 to 2008 and chief financial officer at Biovail Corporation from 2004 to 2006. He previously held finance and operational positions of increasing responsibility at Breakaway Technologies, Inc., Pharmacia, Novartis International AG and Bristol-Myers Squibb Company. Mr. Rowland currently serves as a member of the board of directors for Blueprint Medicines Corporation, a public biopharmaceutical company, Viking Therapeutics, a public, clinical-stage biopharmaceutical company, and Orchard Therapeutics, a public, clinical-stage biopharmaceutical company. In addition, Mr. Rowland serves as a member of the board of directors for Generation Bio, a privately held biopharmaceutical company. Previously, he served on the board of directors at Idenix Pharmaceuticals, Inc., Vitae Pharmaceuticals, Inc., Bind Therapeutics Inc. and Aurinia Pharmaceuticals Inc. Mr. Rowland received his B.S. from Saint Joseph's University and M.B.A. from Rutgers University. - Charles A. Rowland, Jr.(小),2014年9月起成为公司董事会成员。目前他担任战略顾问。2008年10月起到2014年1月公司被Shire plc收购,他担任国际制药公司ViroPharma Incorporated的副总裁兼首席财务官。加入ViroPharma前,2006年12月至2008年9月,他曾是Endo Pharmaceuticals Inc.的执行副总裁、首席财务官和临时联合首席执行官,该公司是一家疼痛管理专业制药公司。2004年至2006年,他担任国际制药公司Biovail Corporation的高级副总裁兼首席财务官。之前,他也曾在Breakaway Technologies公司、Pharmacia Corporation、Novartis AG 和Bristol-Myers Squibb Co。任职。目前他任职于BIND Therapeutics公司和Aurina Pharmaceuticals公司的董事会。2013年至2014年8月公司被默克(Merck & Co., Inc.)收购期间,他任职于Idenix Pharmaceuticals公司的董事会。他同时也是费城Financial Executives International的董事会成员。他取得了圣约瑟夫大学(St. Joseph's University)会计学士和罗格斯大学(Rutgers University)工商管理硕士学位。
- Charles A. Rowland, Jr. has served on our board of directors since June 23 2017. Mr. Rowland previously served on the supervisory board of Nabriva Austria from January 2015 until the Redomiciliation. Mr. Rowland served as chief executive officer of Aurinia Pharmaceuticals Inc. from April 2016 to January 2017. Mr. Rowland previously served as vice president and chief financial officer of ViroPharma Incorporated from 2008 until it was acquired by Shire plc in 2014. Prior to joining ViroPharma, Mr. Rowland served as executive vice president and chief financial officer, as well as interim co-chief executive officer, for Endo Pharmaceuticals Inc. from 2006 to 2008 and chief financial officer at Biovail Corporation from 2004 to 2006. He previously held finance and operational positions of increasing responsibility at Breakaway Technologies, Inc., Pharmacia, Novartis International AG and Bristol-Myers Squibb Company. Mr. Rowland currently serves as a member of the board of directors for Blueprint Medicines Corporation, a public biopharmaceutical company, Viking Therapeutics, a public, clinical-stage biopharmaceutical company, and Orchard Therapeutics, a public, clinical-stage biopharmaceutical company. In addition, Mr. Rowland serves as a member of the board of directors for Generation Bio, a privately held biopharmaceutical company. Previously, he served on the board of directors at Idenix Pharmaceuticals, Inc., Vitae Pharmaceuticals, Inc., Bind Therapeutics Inc. and Aurinia Pharmaceuticals Inc. Mr. Rowland received his B.S. from Saint Joseph's University and M.B.A. from Rutgers University.
- Alexis Borisy
-
Alexis Borisy ,自2009年起任Dianthus Therapeutics, Inc.的董事会成员,自2011年起担任董事长。他在2009年共同创立 Foundation Medicine,并在2011年5月担任临时首席执行官。他自2009年以来任Third Rock Ventures的合伙人;Third Rock Ventures是一个生命科学风险资本公司,集中在新公司的形成、发展和策略。他在2011年共同创立了一家肿瘤私营公司Blueprint Medicines Corp.,目前担任临时首席执行官和董事会成员。此外,他自2013年7月以来担任 Warp Drive Bio有限责任公司的主席,专注于基因组学;他从2011年到2013年7月担任首席执行官。他从2007年到2012年担任一家生命科学公司FORMA Therapeutics公司的董事长;FORMA Therapeutics专注于针对癌症的治疗。他在2000年创立CombinatoRx公司,现为Zalicus 公司(纳斯达克:ZLCS);ZLCS是一个药物开发公司;他从2000年到2009年担任其首席执行官和董事会成员。他持有芝加哥大学化学学士学位和哈佛大学文科硕士学位。
Alexis Borisy,was appointed to the Board of Directors on May 9, 2022. He is the co-founder and Chairman of Curie.Bio, a venture capital firm focused on helping entrepreneurial founders launch therapeutics companies. He is also the founder of EQRx, Inc. (NASDAQ:EQRX), a pharmaceutical company founded in 2019 committed to developing and delivering innovative medicines to patients at radically lower prices, and has served as its Executive Chairman since 2021, previously serving as its Chairman and Chief Executive Officer from 2019 to 2021. Prior to founding EQRx, Mr. Borisy cofounded Relay Therapeutics, Inc. (NASDAQ:RLAY), a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies, and has served as its Chairman since 2016 and served as its Chief Executive Officer from 2016 to 2017. He is also a cofounder of Blueprint Medicines Corporation (NASDAQ: BPMC), a precision therapy company focused on genomically defined cancers, rare diseases and cancer immunotherapy, and has served on the board of directors since 2011 and was the Chief Executive Officer from 2013 to 2014. He previously served as Chairman and Director of Foundation Medicine, Inc. (NASDAQ:FMI), a molecular information company dedicated to a transformation in cancer care, which he cofounded, from 2009 to 2018 and also served as its Chief Executive Officer from 2009 to 2011, and previously served on the boards of Editas Medicine, Inc. (NASDAQ:EDIT), a leading gene editing company dedicated to developing gene edited medicines for people living with serious diseases around the world, from 2013 to 2018, Magenta Therapeutics, Inc. (NASDAQ:MGTA), a clinical-stage biotechnology company developing novel medicines designed to bring the curative power of stem cell transplant to more patients, from 2015 to 2022, and Thrive Earlier Detection Corp., a privately held healthcare company dedicated to incorporating earlier cancer detection into routine medical care, from 2019 to 2021. Mr. Borisy was a partner in Third Rock Ventures, LLC, a leading healthcare venture firm focused on advancing disruptive areas of science and medicine to deliver breakthroughs to patients, from 2010 to 2019. He currently serves on the board of directors of several public companies, including Tango Therapeutics, Inc. (NASDAQ:TNGX), a biotechnology company committed to discovering and delivering the next generation of precision cancer medicines, and Revolution Medicines, Inc. (NASDAQ:RVMD), a clinical-stage oncology company developing targeted therapies for RAS-addicted cancers. He also currently serves on the board of directors of the privately held, Celsius Therapeutics, Inc. and Nextech Invest, Ltd. Mr. Borisy is the Chairman of the Board of Trustees of the Boston Museum of Science, and he previously served as Chairman of the National Venture Capital Association. He holds a Master's Degree in chemistry and chemical biology from Harvard University and a Bachelor of Science in chemistry from the University of Chicago. - Alexis Borisy ,自2009年起任Dianthus Therapeutics, Inc.的董事会成员,自2011年起担任董事长。他在2009年共同创立 Foundation Medicine,并在2011年5月担任临时首席执行官。他自2009年以来任Third Rock Ventures的合伙人;Third Rock Ventures是一个生命科学风险资本公司,集中在新公司的形成、发展和策略。他在2011年共同创立了一家肿瘤私营公司Blueprint Medicines Corp.,目前担任临时首席执行官和董事会成员。此外,他自2013年7月以来担任 Warp Drive Bio有限责任公司的主席,专注于基因组学;他从2011年到2013年7月担任首席执行官。他从2007年到2012年担任一家生命科学公司FORMA Therapeutics公司的董事长;FORMA Therapeutics专注于针对癌症的治疗。他在2000年创立CombinatoRx公司,现为Zalicus 公司(纳斯达克:ZLCS);ZLCS是一个药物开发公司;他从2000年到2009年担任其首席执行官和董事会成员。他持有芝加哥大学化学学士学位和哈佛大学文科硕士学位。
- Alexis Borisy,was appointed to the Board of Directors on May 9, 2022. He is the co-founder and Chairman of Curie.Bio, a venture capital firm focused on helping entrepreneurial founders launch therapeutics companies. He is also the founder of EQRx, Inc. (NASDAQ:EQRX), a pharmaceutical company founded in 2019 committed to developing and delivering innovative medicines to patients at radically lower prices, and has served as its Executive Chairman since 2021, previously serving as its Chairman and Chief Executive Officer from 2019 to 2021. Prior to founding EQRx, Mr. Borisy cofounded Relay Therapeutics, Inc. (NASDAQ:RLAY), a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies, and has served as its Chairman since 2016 and served as its Chief Executive Officer from 2016 to 2017. He is also a cofounder of Blueprint Medicines Corporation (NASDAQ: BPMC), a precision therapy company focused on genomically defined cancers, rare diseases and cancer immunotherapy, and has served on the board of directors since 2011 and was the Chief Executive Officer from 2013 to 2014. He previously served as Chairman and Director of Foundation Medicine, Inc. (NASDAQ:FMI), a molecular information company dedicated to a transformation in cancer care, which he cofounded, from 2009 to 2018 and also served as its Chief Executive Officer from 2009 to 2011, and previously served on the boards of Editas Medicine, Inc. (NASDAQ:EDIT), a leading gene editing company dedicated to developing gene edited medicines for people living with serious diseases around the world, from 2013 to 2018, Magenta Therapeutics, Inc. (NASDAQ:MGTA), a clinical-stage biotechnology company developing novel medicines designed to bring the curative power of stem cell transplant to more patients, from 2015 to 2022, and Thrive Earlier Detection Corp., a privately held healthcare company dedicated to incorporating earlier cancer detection into routine medical care, from 2019 to 2021. Mr. Borisy was a partner in Third Rock Ventures, LLC, a leading healthcare venture firm focused on advancing disruptive areas of science and medicine to deliver breakthroughs to patients, from 2010 to 2019. He currently serves on the board of directors of several public companies, including Tango Therapeutics, Inc. (NASDAQ:TNGX), a biotechnology company committed to discovering and delivering the next generation of precision cancer medicines, and Revolution Medicines, Inc. (NASDAQ:RVMD), a clinical-stage oncology company developing targeted therapies for RAS-addicted cancers. He also currently serves on the board of directors of the privately held, Celsius Therapeutics, Inc. and Nextech Invest, Ltd. Mr. Borisy is the Chairman of the Board of Trustees of the Boston Museum of Science, and he previously served as Chairman of the National Venture Capital Association. He holds a Master's Degree in chemistry and chemical biology from Harvard University and a Bachelor of Science in chemistry from the University of Chicago.
- Daniel S. Lynch
-
Daniel S. Lynch,现为Xilio Therapeutics, Inc.的董事;2012年10月担任Omega Alpha SPAC的董事会主席。从2011年5月起,担任董事长,当时他加入Third Rock Ventures, L.P.,成为入驻企业家。2007年10月以来,他为多家私营的生物制药公司提供咨询服务、担任行政职务或董事,包括:Stromedix, Inc,直到2012年2月它被Biogen Idec收购; Avila Therapeutics, Inc. ,直到2012年2月,它被Celgene Corporation收购;BIND Biosciences, Inc;Eleven Biotherapeutics;RaNA Therapeutics;Nimbus Discovery, LLC;Edimer Pharmaceuticals;Ember Therapeutics;Blueprint Medicines。之前,他是ImClone Systems Corporation的首席执行官、首席财务官。作为首席执行官,他领导了该公司的成功转型,重塑辉煌,并确保了癌症新药ERBITUX (Cetuximab)通过FDA的审批;作为首席财务官,他领导了ImClone 、Bristol-Myers Squibb成立大型合资企业的谈判工作。职业生涯早期,他在Bristol-Myers Squibb工作了15年,担任过各种财务职位。他在U.S. Oncology担任了5年的董事、审核委员会成员,直到2010年12月它被McKesson收购。他在Wesleyan University获得数学学士学位,在Darden Graduate School of Business Administration at the University of Virginia获得工商管理硕士学位。
Daniel S. Lynch,has served as a member of 2seventy Bio, Inc. Board of Directors since October 15, 2021. Prior to the separation by bluebird bio of its oncology portfolio and programs into 2seventy bio, which 2seventy Bio, Inc. refer to as the separation, Mr. Lynch served on the Board of Directors of bluebird bio. Mr. Lynch joined Google Ventures in 2021 as Executive Venture Partner and partners with life sciences CEOs and executives as a trusted advisor. As a coach and investor, he places deep emphasis on long-term relationships. Since 2007, Mr. Lynch has advised and served as an executive chair or member of the boards for multiple biopharmaceutical companies, including Stromedix (acquired by Biogen), Avila Therapeutics (acquired by Celgene Corporation), Nimbus Discovery, Edimer Pharmaceuticals, Ember Therapeutics, Proclara Biosciences, Surface Oncology, Sesen Bio (formerly Eleven Biotherapeutics), Xilio Therapeutics, eGenesis Bio, BIND Biosciences, and Blueprint Medicines. Mr. Lynch currently serves on the board of SpringWorks Therapeutics. He also served as an entrepreneur in residence and venture partner at Third Rock Ventures and was a senior advisor at the firm until 2021. Previously, Mr. Lynch served as CEO and CFO of ImClone Systems Corporation. As CEO, he led the company through a significant turnaround, helping to restore its reputation and secure FDA approval of the novel cancer treatment ERBITUX (Cetuximab). As CFO, Mr. Lynch led negotiations to form a major partnership between ImClone and Bristol-Myers Squibb. Earlier in his career, he held several financial positions at Bristol-Myers Squibb for over 15 years. For five years, he served on the board of directors and the audit committee at U.S. Oncology, Inc. until its acquisition by McKesson in 2010. Mr. Lynch received his B.A. in mathematics from Wesleyan University and his M.B.A. from the Darden Graduate School of Business Administration at The University of Virginia. - Daniel S. Lynch,现为Xilio Therapeutics, Inc.的董事;2012年10月担任Omega Alpha SPAC的董事会主席。从2011年5月起,担任董事长,当时他加入Third Rock Ventures, L.P.,成为入驻企业家。2007年10月以来,他为多家私营的生物制药公司提供咨询服务、担任行政职务或董事,包括:Stromedix, Inc,直到2012年2月它被Biogen Idec收购; Avila Therapeutics, Inc. ,直到2012年2月,它被Celgene Corporation收购;BIND Biosciences, Inc;Eleven Biotherapeutics;RaNA Therapeutics;Nimbus Discovery, LLC;Edimer Pharmaceuticals;Ember Therapeutics;Blueprint Medicines。之前,他是ImClone Systems Corporation的首席执行官、首席财务官。作为首席执行官,他领导了该公司的成功转型,重塑辉煌,并确保了癌症新药ERBITUX (Cetuximab)通过FDA的审批;作为首席财务官,他领导了ImClone 、Bristol-Myers Squibb成立大型合资企业的谈判工作。职业生涯早期,他在Bristol-Myers Squibb工作了15年,担任过各种财务职位。他在U.S. Oncology担任了5年的董事、审核委员会成员,直到2010年12月它被McKesson收购。他在Wesleyan University获得数学学士学位,在Darden Graduate School of Business Administration at the University of Virginia获得工商管理硕士学位。
- Daniel S. Lynch,has served as a member of 2seventy Bio, Inc. Board of Directors since October 15, 2021. Prior to the separation by bluebird bio of its oncology portfolio and programs into 2seventy bio, which 2seventy Bio, Inc. refer to as the separation, Mr. Lynch served on the Board of Directors of bluebird bio. Mr. Lynch joined Google Ventures in 2021 as Executive Venture Partner and partners with life sciences CEOs and executives as a trusted advisor. As a coach and investor, he places deep emphasis on long-term relationships. Since 2007, Mr. Lynch has advised and served as an executive chair or member of the boards for multiple biopharmaceutical companies, including Stromedix (acquired by Biogen), Avila Therapeutics (acquired by Celgene Corporation), Nimbus Discovery, Edimer Pharmaceuticals, Ember Therapeutics, Proclara Biosciences, Surface Oncology, Sesen Bio (formerly Eleven Biotherapeutics), Xilio Therapeutics, eGenesis Bio, BIND Biosciences, and Blueprint Medicines. Mr. Lynch currently serves on the board of SpringWorks Therapeutics. He also served as an entrepreneur in residence and venture partner at Third Rock Ventures and was a senior advisor at the firm until 2021. Previously, Mr. Lynch served as CEO and CFO of ImClone Systems Corporation. As CEO, he led the company through a significant turnaround, helping to restore its reputation and secure FDA approval of the novel cancer treatment ERBITUX (Cetuximab). As CFO, Mr. Lynch led negotiations to form a major partnership between ImClone and Bristol-Myers Squibb. Earlier in his career, he held several financial positions at Bristol-Myers Squibb for over 15 years. For five years, he served on the board of directors and the audit committee at U.S. Oncology, Inc. until its acquisition by McKesson in 2010. Mr. Lynch received his B.A. in mathematics from Wesleyan University and his M.B.A. from the Darden Graduate School of Business Administration at The University of Virginia.
- Daniel S. Lynch
-
Daniel S. Lynch,现为本公司的董事;从2011年5月起,担任董事长,当时他加入Third Rock Ventures, L.P.,成为入驻企业家。2007年10月以来,他为多家私营的生物制药公司提供咨询服务、担任行政职务或董事,包括:Stromedix, Inc,直到2012年2月它被Biogen Idec收购; Avila Therapeutics, Inc. ,直到2012年2月,它被Celgene Corporation收购;BIND Biosciences, Inc;Eleven Biotherapeutics;RaNA Therapeutics;Nimbus Discovery, LLC;Edimer Pharmaceuticals;Ember Therapeutics;Blueprint Medicines。之前,他是ImClone Systems Corporation的首席执行官、首席财务官。作为首席执行官,他领导了该公司的成功转型,重塑辉煌,并确保了癌症新药ERBITUX (Cetuximab)通过FDA的审批;作为首席财务官,他领导了ImClone 、Bristol-Myers Squibb成立大型合资企业的谈判工作。职业生涯早期,他在Bristol-Myers Squibb工作了15年,担任过各种财务职位。他在U.S. Oncology担任了5年的董事、审核委员会成员,直到2010年12月它被McKesson收购。他在Wesleyan University获得数学学士学位,在Darden Graduate School of Business Administration at the University of Virginia获得工商管理硕士学位。
Daniel S. Lynch has served as a member of our board of directors and as chairman of our board of directors since June 2020. Mr. Lynch has served as executive venture partner at GV, a venture capital firm, since March 2021. Mr. Lynch previously served as the interim chief executive officer of Surface Oncology, Inc., or Surface, a pharmaceutical company, from September 2017 until January 2018. He served as an advisor to Third Rock Ventures, a venture capital firm, from December 2016 to March 2021 as a venture partner from May 2013 to December 2016 and as an entrepreneur-in-residence from May 2011 to May 2013. Mr. Lynch serves as a member of the boards of directors of bluebird bio, Inc., a biopharmaceutical company, SpringWorks Therapeutics, Inc., a biopharmaceutical company, and Omega Alpha SPAC. Within the past five years, he served as a member of the boards of directors for the following biotechnology companies: Surface Oncology, Inc., or Surface Oncology, Blueprint Medicines Corporation, Translate Bio, Inc., and Sesen Bio, Inc. Mr. Lynch received a B.A. in mathematics from Wesleyan University and an M.B.A. from the Darden Graduate School of Business Administration at the University of Virginia. - Daniel S. Lynch,现为本公司的董事;从2011年5月起,担任董事长,当时他加入Third Rock Ventures, L.P.,成为入驻企业家。2007年10月以来,他为多家私营的生物制药公司提供咨询服务、担任行政职务或董事,包括:Stromedix, Inc,直到2012年2月它被Biogen Idec收购; Avila Therapeutics, Inc. ,直到2012年2月,它被Celgene Corporation收购;BIND Biosciences, Inc;Eleven Biotherapeutics;RaNA Therapeutics;Nimbus Discovery, LLC;Edimer Pharmaceuticals;Ember Therapeutics;Blueprint Medicines。之前,他是ImClone Systems Corporation的首席执行官、首席财务官。作为首席执行官,他领导了该公司的成功转型,重塑辉煌,并确保了癌症新药ERBITUX (Cetuximab)通过FDA的审批;作为首席财务官,他领导了ImClone 、Bristol-Myers Squibb成立大型合资企业的谈判工作。职业生涯早期,他在Bristol-Myers Squibb工作了15年,担任过各种财务职位。他在U.S. Oncology担任了5年的董事、审核委员会成员,直到2010年12月它被McKesson收购。他在Wesleyan University获得数学学士学位,在Darden Graduate School of Business Administration at the University of Virginia获得工商管理硕士学位。
- Daniel S. Lynch has served as a member of our board of directors and as chairman of our board of directors since June 2020. Mr. Lynch has served as executive venture partner at GV, a venture capital firm, since March 2021. Mr. Lynch previously served as the interim chief executive officer of Surface Oncology, Inc., or Surface, a pharmaceutical company, from September 2017 until January 2018. He served as an advisor to Third Rock Ventures, a venture capital firm, from December 2016 to March 2021 as a venture partner from May 2013 to December 2016 and as an entrepreneur-in-residence from May 2011 to May 2013. Mr. Lynch serves as a member of the boards of directors of bluebird bio, Inc., a biopharmaceutical company, SpringWorks Therapeutics, Inc., a biopharmaceutical company, and Omega Alpha SPAC. Within the past five years, he served as a member of the boards of directors for the following biotechnology companies: Surface Oncology, Inc., or Surface Oncology, Blueprint Medicines Corporation, Translate Bio, Inc., and Sesen Bio, Inc. Mr. Lynch received a B.A. in mathematics from Wesleyan University and an M.B.A. from the Darden Graduate School of Business Administration at the University of Virginia.
- Mark Goldberg
-
Mark Goldberg,自2014年1月起担任Synageva BioPharma Corp.(一家生物制药公司)的医疗和监管策略执行副总裁;2011年9月至2014年1月,担任Synageva BioPharma Corp.的医疗和监管事务高级副总裁。1996年至2011年7月间,Goldberg博士在Genzyme Corporation(一家生物技术公司)担任过多个高管职位,最近担任其临床发展高级副总裁、肿瘤学和个性化遗传健康全球治疗组组长。在Genzyme Corporation工作之前,他曾是Brigham and Women’s Hospital 和 Dana Farber Cancer Institute的全职医师,目前仍有其职位。自1996年起,他也是 Harvard Medical School的临床医学助教。 Goldberg博士是一名认证医疗肿瘤学家和血液学家,拥有50多份出版论文。 Goldberg博士也是ImmunoGen, Inc.的董事,早前曾是Synageva BioPharma Corp.的董事。Goldberg博士获得了Harvard College 的学士学位,和Harvard Medical School的医学博士学位。
Mark Goldberg has served as a member of the board of directors of ImmunoGen, Inc. since November 2011 a member of the board of directors of GlycoMimetics, Inc. since July 2014 and as a member of the board of directors of Blueprint Medicines since June 2015. In addition, he is a member of the board of directors of the American Cancer Society, a non-profit organization. Dr. Goldberg previously served on the board of directors of Audentes Therapeutics, Inc. from December 2017 until January 2020 and aTyr Pharma from April 2015 until December 2017. Dr. Goldberg served as advisor and medical and regulatory strategist for Synageva BioPharma Corp., a biopharmaceutical company, from October 2014 until June 2015. Prior to that, he served as the Executive Vice President for Medical and Regulatory Strategy of Synageva from January 2014 to October 2014 and as the Senior Vice President of Medical and Regulatory Affairs of Synageva from September 2011 to January 2014. Dr. Goldberg served in a variety of senior management positions at Genzyme Corporation from 1996 to July 2011 including most recently as Senior Vice President for Clinical Development and Therapeutic Group Head for Oncology and Personalized Genetic Health from 2009 to July 2011. Prior to working at Genzyme Corporation, he was a full-time staff physician at Brigham and Women's Hospital and Dana Farber Cancer Institute, where he still holds appointments. He has also been an Associate Professor of Medicine at Harvard Medical School since 1996. Dr. Goldberg is a board-certified medical oncologist and hematologist and has more than 50 published papers. Dr. Goldberg holds an A.B. from Harvard College and an M.D. from Harvard Medical School. - Mark Goldberg,自2014年1月起担任Synageva BioPharma Corp.(一家生物制药公司)的医疗和监管策略执行副总裁;2011年9月至2014年1月,担任Synageva BioPharma Corp.的医疗和监管事务高级副总裁。1996年至2011年7月间,Goldberg博士在Genzyme Corporation(一家生物技术公司)担任过多个高管职位,最近担任其临床发展高级副总裁、肿瘤学和个性化遗传健康全球治疗组组长。在Genzyme Corporation工作之前,他曾是Brigham and Women’s Hospital 和 Dana Farber Cancer Institute的全职医师,目前仍有其职位。自1996年起,他也是 Harvard Medical School的临床医学助教。 Goldberg博士是一名认证医疗肿瘤学家和血液学家,拥有50多份出版论文。 Goldberg博士也是ImmunoGen, Inc.的董事,早前曾是Synageva BioPharma Corp.的董事。Goldberg博士获得了Harvard College 的学士学位,和Harvard Medical School的医学博士学位。
- Mark Goldberg has served as a member of the board of directors of ImmunoGen, Inc. since November 2011 a member of the board of directors of GlycoMimetics, Inc. since July 2014 and as a member of the board of directors of Blueprint Medicines since June 2015. In addition, he is a member of the board of directors of the American Cancer Society, a non-profit organization. Dr. Goldberg previously served on the board of directors of Audentes Therapeutics, Inc. from December 2017 until January 2020 and aTyr Pharma from April 2015 until December 2017. Dr. Goldberg served as advisor and medical and regulatory strategist for Synageva BioPharma Corp., a biopharmaceutical company, from October 2014 until June 2015. Prior to that, he served as the Executive Vice President for Medical and Regulatory Strategy of Synageva from January 2014 to October 2014 and as the Senior Vice President of Medical and Regulatory Affairs of Synageva from September 2011 to January 2014. Dr. Goldberg served in a variety of senior management positions at Genzyme Corporation from 1996 to July 2011 including most recently as Senior Vice President for Clinical Development and Therapeutic Group Head for Oncology and Personalized Genetic Health from 2009 to July 2011. Prior to working at Genzyme Corporation, he was a full-time staff physician at Brigham and Women's Hospital and Dana Farber Cancer Institute, where he still holds appointments. He has also been an Associate Professor of Medicine at Harvard Medical School since 1996. Dr. Goldberg is a board-certified medical oncologist and hematologist and has more than 50 published papers. Dr. Goldberg holds an A.B. from Harvard College and an M.D. from Harvard Medical School.
高管简历
中英对照 |  中文 |  英文- Jeffrey W. Albers
Jeffrey W. Albers自2014年7月起一直担任公司首席执行官及总裁和我们的董事会成员。Albers先生生物制药行业担任近十年的领导职务。2012年1月至2014年4月,加入我们之前,他是Algeta ASA或Algeta U.S。(一家挪威的生物制药公司)美国分公司的总裁,在那里他负责商业和商务职务。在Algeta U.S.,Albers先生负责在美国推出治疗转移性阉割性前列腺癌的镭223。在Algeta U.S。之前,2005年7月至2011年11月,Albers先生任职于Genzyme公司(或Genzyme)。Genzyme是一个生物技术公司,现在是Sanofi S.A.的全资子公司,最近担任美国血液学和肿瘤药品事业部的副总裁。Albers先生获得Indiana University学士学位和Indiana University, Georgetown University法学博士学位。
Jeffrey W. Albers has served as our president and chief executive officer and a member of our board of directors since July 2014. In addition, Mr. Albers currently serves on the board of directors of Magenta Therapeutics, Inc., a privately held biopharmaceutical company, and on the board of directors of the New England Division of the American Cancer Society. Prior to joining us, from January 2012 to April 2014 he was president of Algeta ASA, or Algeta, a Norwegian biopharmaceutical company, where he oversaw the commercial and business functions. At Algeta, Mr. Albers was responsible for the U.S. launch of Radium‑223 in metastatic castrate resistant prostate cancer. Prior to Algeta, from July 2005 to November 2011 Mr. Albers was at Genzyme Corporation, or Genzyme, a biotechnology company that is now a wholly-owned subsidiary of Sanofi S.A., most recently as vice president of the U.S. hematology and oncology business unit. Mr. Albers received a B.S. from Indiana University and an M.B.A. and a J.D. from Georgetown University.- Jeffrey W. Albers自2014年7月起一直担任公司首席执行官及总裁和我们的董事会成员。Albers先生生物制药行业担任近十年的领导职务。2012年1月至2014年4月,加入我们之前,他是Algeta ASA或Algeta U.S。(一家挪威的生物制药公司)美国分公司的总裁,在那里他负责商业和商务职务。在Algeta U.S.,Albers先生负责在美国推出治疗转移性阉割性前列腺癌的镭223。在Algeta U.S。之前,2005年7月至2011年11月,Albers先生任职于Genzyme公司(或Genzyme)。Genzyme是一个生物技术公司,现在是Sanofi S.A.的全资子公司,最近担任美国血液学和肿瘤药品事业部的副总裁。Albers先生获得Indiana University学士学位和Indiana University, Georgetown University法学博士学位。
- Jeffrey W. Albers has served as our president and chief executive officer and a member of our board of directors since July 2014. In addition, Mr. Albers currently serves on the board of directors of Magenta Therapeutics, Inc., a privately held biopharmaceutical company, and on the board of directors of the New England Division of the American Cancer Society. Prior to joining us, from January 2012 to April 2014 he was president of Algeta ASA, or Algeta, a Norwegian biopharmaceutical company, where he oversaw the commercial and business functions. At Algeta, Mr. Albers was responsible for the U.S. launch of Radium‑223 in metastatic castrate resistant prostate cancer. Prior to Algeta, from July 2005 to November 2011 Mr. Albers was at Genzyme Corporation, or Genzyme, a biotechnology company that is now a wholly-owned subsidiary of Sanofi S.A., most recently as vice president of the U.S. hematology and oncology business unit. Mr. Albers received a B.S. from Indiana University and an M.B.A. and a J.D. from Georgetown University.
- Anthony L. Boral
Anthony L. Boral,医学博士,博士,自2016年1月起担任Blueprint Medicines Corporation首席医疗官,此前曾于2015年2月至2015年12月担任Blueprint Medicines Corporation临床开发高级副总裁。在加入Blueprint Medicines Corporation之前,Boral博士于2010年11月至2015年2月在诺华生物医学研究所或诺华担任肿瘤临床研究执行董事,自2013年起担任马萨诸塞州剑桥站点的副站点负责人。在诺华,Boral博士负责各种首次人体化合物的临床方面,包括最近的色瑞替尼(一种间变性淋巴瘤激酶抑制剂)和诺华免疫检查点抑制剂项目。在加入诺华之前,他于2002年至2010年在马萨诸塞州剑桥市的生物技术公司Millennium Pharmaceuticals,Inc.或Millennium工作,该公司现在是Takeda Pharmaceutical Company Limited或武田的全资子公司,包括从2007年10月至2010年10月担任肿瘤临床研究副总裁。在Millennium,Boral博士负责VELCADE开发的各个方面,VELCADE是一种一流的癌症疗法,现已被批准用于治疗多发性骨髓瘤和非霍奇金淋巴瘤。Boral博士获得了学士学位。来自卫斯理大学,拥有医学博士和博士学位。来自纽约阿尔伯特爱因斯坦医学院。
Anthony L. Boral, M.D., Ph.D. has served as Blueprint Medicines Corporation chief medical officer since January 2016 and previously served as Blueprint Medicines Corporation senior vice president, clinical development from February 2015 to December 2015. Prior to joining Blueprint Medicines Corporation, from November 2010 to February 2015 Dr. Boral worked at the Novartis Institutes for BioMedical Research, or Novartis, as executive director, oncology clinical research, serving as deputy site head for the Cambridge, Massachusetts site since 2013. At Novartis, Dr. Boral was responsible for the clinical aspects of various first-in-human compounds, including most recently ceritinib, an anaplastic lymphoma kinase inhibitor, and Novartis' immune checkpoint inhibitor programs. Prior to Novartis, from 2002 to 2010 he worked at Millennium Pharmaceuticals, Inc., or Millennium, a biotechnology company in Cambridge, Massachusetts, which is now a wholly-owned subsidiary of Takeda Pharmaceutical Company Limited, or Takeda, including as vice president of oncology clinical research from October 2007 to October 2010. At Millennium, Dr. Boral was responsible for various aspects of the development of VELCADE, a first-in-class cancer therapy now approved to treat multiple myeloma and non-Hodgkin's lymphoma. Dr. Boral received a B.A. from Wesleyan University, and an M.D. and a Ph.D. from the Albert Einstein College of Medicine, in New York.- Anthony L. Boral,医学博士,博士,自2016年1月起担任Blueprint Medicines Corporation首席医疗官,此前曾于2015年2月至2015年12月担任Blueprint Medicines Corporation临床开发高级副总裁。在加入Blueprint Medicines Corporation之前,Boral博士于2010年11月至2015年2月在诺华生物医学研究所或诺华担任肿瘤临床研究执行董事,自2013年起担任马萨诸塞州剑桥站点的副站点负责人。在诺华,Boral博士负责各种首次人体化合物的临床方面,包括最近的色瑞替尼(一种间变性淋巴瘤激酶抑制剂)和诺华免疫检查点抑制剂项目。在加入诺华之前,他于2002年至2010年在马萨诸塞州剑桥市的生物技术公司Millennium Pharmaceuticals,Inc.或Millennium工作,该公司现在是Takeda Pharmaceutical Company Limited或武田的全资子公司,包括从2007年10月至2010年10月担任肿瘤临床研究副总裁。在Millennium,Boral博士负责VELCADE开发的各个方面,VELCADE是一种一流的癌症疗法,现已被批准用于治疗多发性骨髓瘤和非霍奇金淋巴瘤。Boral博士获得了学士学位。来自卫斯理大学,拥有医学博士和博士学位。来自纽约阿尔伯特爱因斯坦医学院。
- Anthony L. Boral, M.D., Ph.D. has served as Blueprint Medicines Corporation chief medical officer since January 2016 and previously served as Blueprint Medicines Corporation senior vice president, clinical development from February 2015 to December 2015. Prior to joining Blueprint Medicines Corporation, from November 2010 to February 2015 Dr. Boral worked at the Novartis Institutes for BioMedical Research, or Novartis, as executive director, oncology clinical research, serving as deputy site head for the Cambridge, Massachusetts site since 2013. At Novartis, Dr. Boral was responsible for the clinical aspects of various first-in-human compounds, including most recently ceritinib, an anaplastic lymphoma kinase inhibitor, and Novartis' immune checkpoint inhibitor programs. Prior to Novartis, from 2002 to 2010 he worked at Millennium Pharmaceuticals, Inc., or Millennium, a biotechnology company in Cambridge, Massachusetts, which is now a wholly-owned subsidiary of Takeda Pharmaceutical Company Limited, or Takeda, including as vice president of oncology clinical research from October 2007 to October 2010. At Millennium, Dr. Boral was responsible for various aspects of the development of VELCADE, a first-in-class cancer therapy now approved to treat multiple myeloma and non-Hodgkin's lymphoma. Dr. Boral received a B.A. from Wesleyan University, and an M.D. and a Ph.D. from the Albert Einstein College of Medicine, in New York.
- Kathryn Haviland
Kathryn Haviland自2016年1月起担任Blueprint Medicines Corporation首席商务官。在加入Blueprint Medicines Corporation之前,2014年4月至2015年12月,Haviland女士担任Idera Pharmaceuticals, Inc.罕见病和肿瘤项目领导副总裁,负责监督Idera罕见病和肿瘤管道项目的产品开发战略的各个方面,包括临床前研究、制造和药物供应、监管事务、临床开发和执行以及商业规划。在加入Idera之前,Haviland女士于2012年6月至2014年4月担任Sarepta Therapeutics, Inc.的商业开发主管,负责产品开发和商业规划,并培养与主要意见领袖和患者权益团体的关系。此外,Haviland女士曾于2007年4月至2012年6月担任Ptc Therapeutics公司商业开发执行董事,并于2005年7月至2007年4月在健赞担任企业开发和项目管理职务。Haviland女士获得了学士学位,来自卫斯理大学,拥有生物化学/分子生物学和经济学双学士学位,以及哈佛商学院的工商管理硕士学位。
Kathryn Haviland has served as Blueprint Medicines Corporation chief business officer since January 2016. Prior to joining Blueprint Medicines Corporation, from April 2014 to December 2015 Ms. Haviland served as vice president, rare diseases and oncology program leadership at Idera Pharmaceuticals, Inc., or Idera, where she oversaw all aspects of the product development strategy for Idera's rare disease and oncology pipeline programs, including preclinical research, manufacturing and drug supply, regulatory affairs, clinical development and execution and commercial planning. Prior to joining Idera, from June 2012 to April 2014 Ms. Haviland served as head of commercial development at Sarepta Therapeutics, Inc. where she was responsible for product development and commercial planning and for cultivating relationships with key opinion leaders and patient advocacy groups. In addition, Ms. Haviland previously served as executive director of commercial development at PTC Therapeutics, Inc. from April 2007 to June 2012 and held corporate development and project management roles at Genzyme from July 2005 to April 2007. Ms. Haviland received a B.A. from Wesleyan University with a double major in biochemistry/molecular biology and economics and an M.B.A. from Harvard Business School.- Kathryn Haviland自2016年1月起担任Blueprint Medicines Corporation首席商务官。在加入Blueprint Medicines Corporation之前,2014年4月至2015年12月,Haviland女士担任Idera Pharmaceuticals, Inc.罕见病和肿瘤项目领导副总裁,负责监督Idera罕见病和肿瘤管道项目的产品开发战略的各个方面,包括临床前研究、制造和药物供应、监管事务、临床开发和执行以及商业规划。在加入Idera之前,Haviland女士于2012年6月至2014年4月担任Sarepta Therapeutics, Inc.的商业开发主管,负责产品开发和商业规划,并培养与主要意见领袖和患者权益团体的关系。此外,Haviland女士曾于2007年4月至2012年6月担任Ptc Therapeutics公司商业开发执行董事,并于2005年7月至2007年4月在健赞担任企业开发和项目管理职务。Haviland女士获得了学士学位,来自卫斯理大学,拥有生物化学/分子生物学和经济学双学士学位,以及哈佛商学院的工商管理硕士学位。
- Kathryn Haviland has served as Blueprint Medicines Corporation chief business officer since January 2016. Prior to joining Blueprint Medicines Corporation, from April 2014 to December 2015 Ms. Haviland served as vice president, rare diseases and oncology program leadership at Idera Pharmaceuticals, Inc., or Idera, where she oversaw all aspects of the product development strategy for Idera's rare disease and oncology pipeline programs, including preclinical research, manufacturing and drug supply, regulatory affairs, clinical development and execution and commercial planning. Prior to joining Idera, from June 2012 to April 2014 Ms. Haviland served as head of commercial development at Sarepta Therapeutics, Inc. where she was responsible for product development and commercial planning and for cultivating relationships with key opinion leaders and patient advocacy groups. In addition, Ms. Haviland previously served as executive director of commercial development at PTC Therapeutics, Inc. from April 2007 to June 2012 and held corporate development and project management roles at Genzyme from July 2005 to April 2007. Ms. Haviland received a B.A. from Wesleyan University with a double major in biochemistry/molecular biology and economics and an M.B.A. from Harvard Business School.
- Michael Landsittel
Michael Landsittel,自2016年2月起担任公司财务副总裁,此前2014年9月至2016年2月担任财务高级主管。进入公司前,2012年10月至2014年7月,Mr. Landsittel曾担任Algeta U.S。高级财务主管。进入Algeta前,2012年3月至2012年10月,Mr. Landsittel曾担任Infinity Pharmaceuticals, Inc.财务主管,2002年8月至2012年3月Mr. Landsittel曾在Genzyme担任若干业务发展和战略策划的职务,最近担任商务规划部主管。Mr. Landsittel在Arthur Andersen LLP开始他的职业生涯,他获得了伊利诺斯州注册会计师执照。Mr. Landsittel获得了University of Michigan工商管理学士学位和Dartmouth College塔克商学院工商管理硕士学位。
Michael Landsittel has served as our vice president, finance since February 2016 and previously served as our senior director, finance from September 2014 to February 2016. Prior to joining us, from October 2012 to July 2014 Mr. Landsittel served as senior director, finance at Algeta Prior to his time at Algeta, from March 2012 to October 2012 Mr. Landsittel served as director, finance at Infinity Pharmaceuticals, Inc., and from August 2002 to March 2012 Mr. Landsittel held various business development and strategic planning roles of increasing responsibility at Genzyme, including most recently as director, business planning. Mr. Landsittel began his career at Arthur Andersen LLP, and he earned his certified public accountant license in Illinois. Mr. Landsittel received a B.B.A from the University of Michigan and an M.B.A. from the Tuck School of Business at Dartmouth College.- Michael Landsittel,自2016年2月起担任公司财务副总裁,此前2014年9月至2016年2月担任财务高级主管。进入公司前,2012年10月至2014年7月,Mr. Landsittel曾担任Algeta U.S。高级财务主管。进入Algeta前,2012年3月至2012年10月,Mr. Landsittel曾担任Infinity Pharmaceuticals, Inc.财务主管,2002年8月至2012年3月Mr. Landsittel曾在Genzyme担任若干业务发展和战略策划的职务,最近担任商务规划部主管。Mr. Landsittel在Arthur Andersen LLP开始他的职业生涯,他获得了伊利诺斯州注册会计师执照。Mr. Landsittel获得了University of Michigan工商管理学士学位和Dartmouth College塔克商学院工商管理硕士学位。
- Michael Landsittel has served as our vice president, finance since February 2016 and previously served as our senior director, finance from September 2014 to February 2016. Prior to joining us, from October 2012 to July 2014 Mr. Landsittel served as senior director, finance at Algeta Prior to his time at Algeta, from March 2012 to October 2012 Mr. Landsittel served as director, finance at Infinity Pharmaceuticals, Inc., and from August 2002 to March 2012 Mr. Landsittel held various business development and strategic planning roles of increasing responsibility at Genzyme, including most recently as director, business planning. Mr. Landsittel began his career at Arthur Andersen LLP, and he earned his certified public accountant license in Illinois. Mr. Landsittel received a B.B.A from the University of Michigan and an M.B.A. from the Tuck School of Business at Dartmouth College.
- Marion Dorsch
Marion Dorsch博士自2016年11月起担任我们的首席科学官。在加入我们之前,从2012年4月到2016年11月,Dorsch博士担任Agios制药公司(Agios)的生物学Vice President。在该职位上,她负责Agios’;癌症,罕见遗传病和免疫肿瘤学组合中的新颖目标验证,药物发现和生物标志物策略。在Agios任职期间,Dorsch博士为将几个针对定义的遗传损伤的分子成功推进到临床试验做出了贡献。加入Agios公司之前,她曾担任Sanofi Oncology公司的癌症生物学董事,在那里她曾监管药物发现工作。在她职业生涯的早期,Dorsch博士在Novartis Institute for Biomedical Research担任Sonidegib Odomzo(现已在美国和欧盟批准用于治疗局部晚期基底细胞癌)的研究项目负责人,还在Millennium Pharmaceuticals,Inc.从事炎症发现工作。Dorsch博士在德国柏林自由大学(Free University of Berlin)获得肿瘤免疫学博士学位,曾是纽约哥伦比亚大学(Columbia University)的博士后。
Marion Dorsch, Ph.D. has served as our chief scientific officer since November 2016. Prior to joining us, from April 2012 to November 2016 Dr. Dorsch served as Vice President of Biology at Agios Pharmaceuticals, Inc., or Agios. In this role, she was responsible for novel target validation, drug discovery, and biomarker strategy across Agios’ cancer, rare genetic diseases and immuno-oncology portfolios. During her tenure at Agios, Dr. Dorsch contributed to the successful advancement of several molecules targeting defined genetic lesions into clinical trials. Prior to joining Agios, Dr. Dorsch was the Director of Cancer Biology at Sanofi Oncology, where she oversaw drug discovery efforts. Earlier in her career, Dr. Dorsch served as research project leader for sonidegib Odomzo, now approved in the United States and European Union for the treatment of locally advanced basal cell carcinoma, at the Novartis Institutes for Biomedical Research and also worked in Inflammation Discovery at Millennium Pharmaceuticals, Inc. Dr. Dorsch received her Ph.D. in Tumor Immunology from the Free University of Berlin, Germany and was a postdoctoral fellow at Columbia University in New York.- Marion Dorsch博士自2016年11月起担任我们的首席科学官。在加入我们之前,从2012年4月到2016年11月,Dorsch博士担任Agios制药公司(Agios)的生物学Vice President。在该职位上,她负责Agios’;癌症,罕见遗传病和免疫肿瘤学组合中的新颖目标验证,药物发现和生物标志物策略。在Agios任职期间,Dorsch博士为将几个针对定义的遗传损伤的分子成功推进到临床试验做出了贡献。加入Agios公司之前,她曾担任Sanofi Oncology公司的癌症生物学董事,在那里她曾监管药物发现工作。在她职业生涯的早期,Dorsch博士在Novartis Institute for Biomedical Research担任Sonidegib Odomzo(现已在美国和欧盟批准用于治疗局部晚期基底细胞癌)的研究项目负责人,还在Millennium Pharmaceuticals,Inc.从事炎症发现工作。Dorsch博士在德国柏林自由大学(Free University of Berlin)获得肿瘤免疫学博士学位,曾是纽约哥伦比亚大学(Columbia University)的博士后。
- Marion Dorsch, Ph.D. has served as our chief scientific officer since November 2016. Prior to joining us, from April 2012 to November 2016 Dr. Dorsch served as Vice President of Biology at Agios Pharmaceuticals, Inc., or Agios. In this role, she was responsible for novel target validation, drug discovery, and biomarker strategy across Agios’ cancer, rare genetic diseases and immuno-oncology portfolios. During her tenure at Agios, Dr. Dorsch contributed to the successful advancement of several molecules targeting defined genetic lesions into clinical trials. Prior to joining Agios, Dr. Dorsch was the Director of Cancer Biology at Sanofi Oncology, where she oversaw drug discovery efforts. Earlier in her career, Dr. Dorsch served as research project leader for sonidegib Odomzo, now approved in the United States and European Union for the treatment of locally advanced basal cell carcinoma, at the Novartis Institutes for Biomedical Research and also worked in Inflammation Discovery at Millennium Pharmaceuticals, Inc. Dr. Dorsch received her Ph.D. in Tumor Immunology from the Free University of Berlin, Germany and was a postdoctoral fellow at Columbia University in New York.
- Tracey L. McCain
TraceyL.McCain自2018年2月以来一直担任我们的董事会成员。自2016年9月以来,麦凯恩女士一直担任生物技术公司Blueprint Medicine Corporation(简称Blueprint)的执行Vice President兼首席法律和合规官。在加入Blueprint之前,麦凯恩女士于2016年1月至2016年9月担任赛诺菲Genzyme(赛诺菲S.A.或赛诺菲的全球业务部门)的高级副总裁兼法律主管。McCain从1997年5月到2016年9月在Genzyme担任多个职位,包括2011年Genzyme被Sanofi收购后担任总法律顾问。McCain女士拥有哥伦比亚大学法学院(Columbia University School of Law)的法学博士学位和宾夕法尼亚大学(University of Pennsylvania)的文学学士学位。
Tracey L. McCain has served as a member of our Board of Directors since February 2018. Since September 2016 Ms. McCain has served as Executive Vice President and Chief Legal and Compliance Officer of Blueprint Medicine Corporation, or Blueprint, a biotechnology company. Prior to Blueprint, from January 2016 to September 2016 Ms. McCain was Senior Vice President and Head of Legal for Sanofi Genzyme, a global business unit of Sanofi S.A., or Sanofi. From May 1997 to September 2016 Ms. McCain held various roles at Genzyme, including as General Counsel following Genzyme’s acquisition by Sanofi in 2011. Ms. McCain holds a J.D. from Columbia University School of Law and a B.A. from the University of Pennsylvania.- TraceyL.McCain自2018年2月以来一直担任我们的董事会成员。自2016年9月以来,麦凯恩女士一直担任生物技术公司Blueprint Medicine Corporation(简称Blueprint)的执行Vice President兼首席法律和合规官。在加入Blueprint之前,麦凯恩女士于2016年1月至2016年9月担任赛诺菲Genzyme(赛诺菲S.A.或赛诺菲的全球业务部门)的高级副总裁兼法律主管。McCain从1997年5月到2016年9月在Genzyme担任多个职位,包括2011年Genzyme被Sanofi收购后担任总法律顾问。McCain女士拥有哥伦比亚大学法学院(Columbia University School of Law)的法学博士学位和宾夕法尼亚大学(University of Pennsylvania)的文学学士学位。
- Tracey L. McCain has served as a member of our Board of Directors since February 2018. Since September 2016 Ms. McCain has served as Executive Vice President and Chief Legal and Compliance Officer of Blueprint Medicine Corporation, or Blueprint, a biotechnology company. Prior to Blueprint, from January 2016 to September 2016 Ms. McCain was Senior Vice President and Head of Legal for Sanofi Genzyme, a global business unit of Sanofi S.A., or Sanofi. From May 1997 to September 2016 Ms. McCain held various roles at Genzyme, including as General Counsel following Genzyme’s acquisition by Sanofi in 2011. Ms. McCain holds a J.D. from Columbia University School of Law and a B.A. from the University of Pennsylvania.
- Christopher K. Murray
ChristopherK.Murray博士自2017年10月以来一直担任我们的高级副总裁,技术运营。在加入我们之前,Murray博士于2014年1月至2017年5月担任ARIADPharmaceuticals,Inc.(Ariad)技术运营Vice President。在此职位上,Murray博士监管Ariad’;s批准的产品和候选产品的商业和临床制造,供应链和物流,过程开发,质量控制和分析化学的所有方面,包括Iclusig Ponatinib和Alunbrig(Brigatinib)。从2004年到2013年12月,Murray博士在Ariad担任多个职责递增的职位,涉及过程开发、制造和临床供应。在加入Ariad公司之前,Murray博士曾在AllosTherapeutics,Inc.公司和豪瑟公司担任过与临床和商业制造以及活性药物成分供应有关的多个职位。Murray博士拥有Hope College化学专业的B.S.和芝加哥大学(University of Chicago)化学博士学位。
Christopher K. Murray, Ph.D. has served as our senior vice president, technical operations since October 2017. Prior to joining us, from January 2014 to May 2017 Dr. Murray served as vice president, technical operations at ARIAD Pharmaceuticals, Inc., or ARIAD. In this role, Dr. Murray oversaw all aspects of commercial and clinical manufacturing, supply chain and logistics, process development, quality control and analytical chemistry for ARIAD’s approved products and product candidates, including Iclusig ponatinib and Alunbrig (brigatinib). From 2004 to December 2013 Dr. Murray held multiple roles of increasing responsibility at ARIAD related to process development, manufacturing and clinical supply. Prior to joining ARIAD, Dr. Murray served in various positions with Allos Therapeutics, Inc. and Hauser Inc. related to clinical and commercial manufacturing and supply of active pharmaceutical ingredient. Dr. Murray holds a B.S. from Hope College with a major in chemistry and a Ph.D. in chemistry from the University of Chicago.- ChristopherK.Murray博士自2017年10月以来一直担任我们的高级副总裁,技术运营。在加入我们之前,Murray博士于2014年1月至2017年5月担任ARIADPharmaceuticals,Inc.(Ariad)技术运营Vice President。在此职位上,Murray博士监管Ariad’;s批准的产品和候选产品的商业和临床制造,供应链和物流,过程开发,质量控制和分析化学的所有方面,包括Iclusig Ponatinib和Alunbrig(Brigatinib)。从2004年到2013年12月,Murray博士在Ariad担任多个职责递增的职位,涉及过程开发、制造和临床供应。在加入Ariad公司之前,Murray博士曾在AllosTherapeutics,Inc.公司和豪瑟公司担任过与临床和商业制造以及活性药物成分供应有关的多个职位。Murray博士拥有Hope College化学专业的B.S.和芝加哥大学(University of Chicago)化学博士学位。
- Christopher K. Murray, Ph.D. has served as our senior vice president, technical operations since October 2017. Prior to joining us, from January 2014 to May 2017 Dr. Murray served as vice president, technical operations at ARIAD Pharmaceuticals, Inc., or ARIAD. In this role, Dr. Murray oversaw all aspects of commercial and clinical manufacturing, supply chain and logistics, process development, quality control and analytical chemistry for ARIAD’s approved products and product candidates, including Iclusig ponatinib and Alunbrig (brigatinib). From 2004 to December 2013 Dr. Murray held multiple roles of increasing responsibility at ARIAD related to process development, manufacturing and clinical supply. Prior to joining ARIAD, Dr. Murray served in various positions with Allos Therapeutics, Inc. and Hauser Inc. related to clinical and commercial manufacturing and supply of active pharmaceutical ingredient. Dr. Murray holds a B.S. from Hope College with a major in chemistry and a Ph.D. in chemistry from the University of Chicago.