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 |
|---|---|---|---|---|---|---|
| Khoso Baluch | 男 | Director | 65 | 0.60万美元 | 未持股 | 2023-03-31 |
| Justin Yorke | 男 | Chairman of the Board | 56 | 7.50万美元 | 未持股 | 2023-03-31 |
| Geraldine Pannu | 女 | Director | 53 | 7.50万美元 | 未持股 | 2023-03-31 |
| Khoso Baluch | 男 | Director | 65 | 未披露 | 未持股 | 2023-03-31 |
| James Neal | 男 | Director | 67 | 0.60万美元 | 未持股 | 2023-03-31 |
| Virgil Thompson | 男 | Director | 83 | 7.50万美元 | 未持股 | 2023-03-31 |
| David Young | 男 | President and Chief Executive Officer and Director | 70 | 116.26万美元 | 未持股 | 2023-03-31 |
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 |
|---|---|---|---|---|---|---|
| Patrick Lin | 男 | Chief Business and Strategy Officer | 57 | 104.28万美元 | 未持股 | 2023-03-31 |
| Sian Bigora | 女 | Chief Development Officer | 62 | 107.55万美元 | 未持股 | 2023-03-31 |
| James Stanker | 男 | Chief Financial Officer | 65 | 104.02万美元 | 未持股 | 2023-03-31 |
| Wendy Guy | 女 | Chief Administrative Officer | 58 | 101.98万美元 | 未持股 | 2023-03-31 |
| Michael Floyd | 男 | Chief Operations Officer | 67 | 104.24万美元 | 未持股 | 2023-03-31 |
| David Young | 男 | President and Chief Executive Officer and Director | 70 | 116.26万美元 | 未持股 | 2023-03-31 |
董事简历
中英对照 |  中文 |  英文- Khoso Baluch
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Khoso Baluch于2016年10月被任命为首席执行官后加入我们的董事会。Baluch先生之前曾担任UCB,SA或UCB的高级副总裁兼欧洲,中东和非洲地区总裁,2015年1月至2016年4月,高级副总裁兼UCB欧洲区总裁,2013年2月至2014年12月,高级副总裁兼UCB首席营销官,2010年1月至2013年2月。在加入UCB之前,Baluch先生在礼来公司公司工作了24年,在欧洲、中东和美国担任一般管理、业务发展、市场准入和产品领导方面的国际职位。他曾一直担任Poxel公司(法国上市生物技术公司)的独立董事(2013年以来),也曾担任其薪酬委员会主席。他还担任Poxel SA的业务发展和科学委员会成员。Baluch先生拥有伦敦城市大学(City University London)航空工程学士学位和克兰菲尔德管理学院(Cranfield School of Management)工商管理硕士学位。
Khoso Baluch,has served as a Director since July 2022. He has over 36 years of experience across global geographies in the biopharmaceutical industry. Since 2012, he has served as an independent director of Poxel S.A., a French publicly traded biotech company, and chairs its compensation committee. He has also served as the Chairman of the Board for Da Volterra, a French privately held company, since December 2021. From 2016 to 2021, Mr. Baluch served as the Chief Executive Officer and Board member of CorMedix, Inc., a publicly traded pharmaceutical company in the US. Mr. Baluch also held various senior positions at UCB, S.A. between January 2008 to April 2016, including Senior Vice President and President Europe, Middle East & Africa. Prior to joining UCB, Mr. Baluch worked for Eli Lilly and Company for 24 years, holding international positions spanning Europe, the Middle East and the United States in general management, business development, market access and product leadership. Mr. Baluch holds a B.S. in Aeronautical Engineering from City University London and an MBA from Cranfield School of Management. - Khoso Baluch于2016年10月被任命为首席执行官后加入我们的董事会。Baluch先生之前曾担任UCB,SA或UCB的高级副总裁兼欧洲,中东和非洲地区总裁,2015年1月至2016年4月,高级副总裁兼UCB欧洲区总裁,2013年2月至2014年12月,高级副总裁兼UCB首席营销官,2010年1月至2013年2月。在加入UCB之前,Baluch先生在礼来公司公司工作了24年,在欧洲、中东和美国担任一般管理、业务发展、市场准入和产品领导方面的国际职位。他曾一直担任Poxel公司(法国上市生物技术公司)的独立董事(2013年以来),也曾担任其薪酬委员会主席。他还担任Poxel SA的业务发展和科学委员会成员。Baluch先生拥有伦敦城市大学(City University London)航空工程学士学位和克兰菲尔德管理学院(Cranfield School of Management)工商管理硕士学位。
- Khoso Baluch,has served as a Director since July 2022. He has over 36 years of experience across global geographies in the biopharmaceutical industry. Since 2012, he has served as an independent director of Poxel S.A., a French publicly traded biotech company, and chairs its compensation committee. He has also served as the Chairman of the Board for Da Volterra, a French privately held company, since December 2021. From 2016 to 2021, Mr. Baluch served as the Chief Executive Officer and Board member of CorMedix, Inc., a publicly traded pharmaceutical company in the US. Mr. Baluch also held various senior positions at UCB, S.A. between January 2008 to April 2016, including Senior Vice President and President Europe, Middle East & Africa. Prior to joining UCB, Mr. Baluch worked for Eli Lilly and Company for 24 years, holding international positions spanning Europe, the Middle East and the United States in general management, business development, market access and product leadership. Mr. Baluch holds a B.S. in Aeronautical Engineering from City University London and an MBA from Cranfield School of Management.
- Justin Yorke
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Justin Yorke自2017年10月起担任董事。过去10多年来,他一直担任the San Gabriel Fund、JMW Fund和the Richland Fund的经理,其主要活动是投资美国的公共和私人公司。Yorke先生在JED Oil担任非执行主席,在JMG Exploration担任董事/首席执行官。Yorke曾担任Darier Henstch,S.A.(一家瑞士私人银行)驻香港基金经理和高级金融分析师,管理他们4亿美元的亚洲投资组合。Yorke先生曾是Peregrine Asset Management的助理董事兼高级财务分析师,该公司是Peregrine Securities的一个部门,一家区域性的亚洲投资银行。Yorke先生是瑞士一家私人银行Unifund Global Ltd.的Vice President和高级金融分析师,管理其1.5亿美元的亚洲投资组合。Yorke先生拥有加州大学洛杉矶分校(University of California,Los Angeles)的学士学位。
Justin Yorke,became a member of the Board of the Company on March 31, 2020. Since March 31, 2020, Mr. Yorke has also served as the Company's Secretary. Mr. Yorke has over 25 years of experience in finance. Based in Hong Kong for over 10 years, he managed funds for a private Swiss Bank, Darier Henstch from 1997 to 2000. Prior to that, from 1995 to 1997, Mr. Yorke managed funds for Peregrine Investments and from 1990 to 1995 Unifund, Asia, Ltd, Hong Kong, a high net-worth family office headquartered Geneva, Switzerland. From 2000 to 2004, he was a partner at Asiatic Investment Management, based in San Francisco. Since 2004, Mr. Yorke has been a partner in San Gabriel Advisors, LLC and Arroyo Capital Management, LLC and is the manager of the San Gabriel Fund, JMW Fund and Richland Fund. The funds are highly diversified in focus with investment holdings, public, private equity and debt investments and real estate investments. He has a B.A. degree from UCLA. Mr. Yorke is the principal of WesBev LLC, which prior to the merger between CMS and Splash Beverage Group, Inc. Company was the majority shareholder of the Company. He also is an acting director and audit committee chair of Processa Pharmaceuticals, (Nasdaq: PCSA). Mr. Yorke served as non-executive Chairman of Jed Oil and a Director/CEO at JMG Exploration. - Justin Yorke自2017年10月起担任董事。过去10多年来,他一直担任the San Gabriel Fund、JMW Fund和the Richland Fund的经理,其主要活动是投资美国的公共和私人公司。Yorke先生在JED Oil担任非执行主席,在JMG Exploration担任董事/首席执行官。Yorke曾担任Darier Henstch,S.A.(一家瑞士私人银行)驻香港基金经理和高级金融分析师,管理他们4亿美元的亚洲投资组合。Yorke先生曾是Peregrine Asset Management的助理董事兼高级财务分析师,该公司是Peregrine Securities的一个部门,一家区域性的亚洲投资银行。Yorke先生是瑞士一家私人银行Unifund Global Ltd.的Vice President和高级金融分析师,管理其1.5亿美元的亚洲投资组合。Yorke先生拥有加州大学洛杉矶分校(University of California,Los Angeles)的学士学位。
- Justin Yorke,became a member of the Board of the Company on March 31, 2020. Since March 31, 2020, Mr. Yorke has also served as the Company's Secretary. Mr. Yorke has over 25 years of experience in finance. Based in Hong Kong for over 10 years, he managed funds for a private Swiss Bank, Darier Henstch from 1997 to 2000. Prior to that, from 1995 to 1997, Mr. Yorke managed funds for Peregrine Investments and from 1990 to 1995 Unifund, Asia, Ltd, Hong Kong, a high net-worth family office headquartered Geneva, Switzerland. From 2000 to 2004, he was a partner at Asiatic Investment Management, based in San Francisco. Since 2004, Mr. Yorke has been a partner in San Gabriel Advisors, LLC and Arroyo Capital Management, LLC and is the manager of the San Gabriel Fund, JMW Fund and Richland Fund. The funds are highly diversified in focus with investment holdings, public, private equity and debt investments and real estate investments. He has a B.A. degree from UCLA. Mr. Yorke is the principal of WesBev LLC, which prior to the merger between CMS and Splash Beverage Group, Inc. Company was the majority shareholder of the Company. He also is an acting director and audit committee chair of Processa Pharmaceuticals, (Nasdaq: PCSA). Mr. Yorke served as non-executive Chairman of Jed Oil and a Director/CEO at JMG Exploration.
- Geraldine Pannu
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Geraldine Pannu,自2022年起担任董事会成员。她是GLTJ Pioneer Capital的管理合伙人,这是一家专门从事开发和固定收益投资的房地产公司。潘努女士是Processa Pharmaceuticals(纳斯达克股票代码:PCSA)的独立董事。她还指导了几家初创公司,并以临时首席财务官的身份协助它们。此前,她是金门国际的董事总经理,该公司是北加州最大的EB5区域中心之一。她曾担任旧金山领先的对冲和风险投资基金公司ChinaRock Capital Management的首席运营官和管理合伙人近10年。她曾在麦肯锡公司、摩立特公司担任管理顾问,在商学院之前和之后都是如此。她成功地为几个对冲基金、风险投资基金和房地产基金筹集了资金。潘努出生于上海,在香港长大。她在香港中文大学获得工商管理学士学位,在哈佛商学院获得工商管理硕士学位。她能说流利的英语、普通话、粤语和上海话。
Geraldine Pannu,has served as a Director since February 2020. Ms. Pannu has over 25 years of experience in investment and financial management, fund operations, consulting and marketing. Since January 2020, she has been the Founding and Managing Partner of GLTJ Pioneer Capital, a firm that specializes in land acquisition, entitlement and vertical development of multifamily, student and senior housing in the San Francisco Bay Area. From March 2007 to December 2016, Ms. Pannu was the COO and Managing Partner for ChinaRock Capital Management, a leading hedge and venture capital fund company. She previously worked at McKinsey & Co., Monitor Company as a management consultant. She has successfully raised capital for several hedge, venture capital and real estate funds. She also helped start-up companies expand and diversify business categories and client verticals and grow revenue. Ms. Pannu was born in Shanghai and grew up in Hong Kong. She received her BBA from the Chinese University of Hong Kong and an MBA from Harvard Business School. She is fluent in English, Mandarin, Cantonese and Shanghainese. - Geraldine Pannu,自2022年起担任董事会成员。她是GLTJ Pioneer Capital的管理合伙人,这是一家专门从事开发和固定收益投资的房地产公司。潘努女士是Processa Pharmaceuticals(纳斯达克股票代码:PCSA)的独立董事。她还指导了几家初创公司,并以临时首席财务官的身份协助它们。此前,她是金门国际的董事总经理,该公司是北加州最大的EB5区域中心之一。她曾担任旧金山领先的对冲和风险投资基金公司ChinaRock Capital Management的首席运营官和管理合伙人近10年。她曾在麦肯锡公司、摩立特公司担任管理顾问,在商学院之前和之后都是如此。她成功地为几个对冲基金、风险投资基金和房地产基金筹集了资金。潘努出生于上海,在香港长大。她在香港中文大学获得工商管理学士学位,在哈佛商学院获得工商管理硕士学位。她能说流利的英语、普通话、粤语和上海话。
- Geraldine Pannu,has served as a Director since February 2020. Ms. Pannu has over 25 years of experience in investment and financial management, fund operations, consulting and marketing. Since January 2020, she has been the Founding and Managing Partner of GLTJ Pioneer Capital, a firm that specializes in land acquisition, entitlement and vertical development of multifamily, student and senior housing in the San Francisco Bay Area. From March 2007 to December 2016, Ms. Pannu was the COO and Managing Partner for ChinaRock Capital Management, a leading hedge and venture capital fund company. She previously worked at McKinsey & Co., Monitor Company as a management consultant. She has successfully raised capital for several hedge, venture capital and real estate funds. She also helped start-up companies expand and diversify business categories and client verticals and grow revenue. Ms. Pannu was born in Shanghai and grew up in Hong Kong. She received her BBA from the Chinese University of Hong Kong and an MBA from Harvard Business School. She is fluent in English, Mandarin, Cantonese and Shanghainese.
- Khoso Baluch
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暂无中文简介
Khoso Baluch,has served as a Director since July 2022. He has over 36 years of experience across global geographies in the biopharmaceutical industry. Since 2012, he has served as an independent director of Poxel S.A., a French publicly traded biotech company, and chairs its compensation committee. He has also served as the Chairman of the Board for Da Volterra, a French privately held company, since December 2021. From 2016 to 2021, Mr. Baluch served as the Chief Executive Officer and Board member of CorMedix, Inc., a publicly traded pharmaceutical company in the US. Mr. Baluch also held various senior positions at UCB, S.A. between January 2008 to April 2016, including Senior Vice President and President Europe, Middle East & Africa. Prior to joining UCB, Mr. Baluch worked for Eli Lilly and Company for 24 years, holding international positions spanning Europe, the Middle East and the United States in general management, business development, market access and product leadership. Mr. Baluch holds a B.S. in Aeronautical Engineering from City University London and an MBA from Cranfield School of Management. -
暂无中文简介
- Khoso Baluch,has served as a Director since July 2022. He has over 36 years of experience across global geographies in the biopharmaceutical industry. Since 2012, he has served as an independent director of Poxel S.A., a French publicly traded biotech company, and chairs its compensation committee. He has also served as the Chairman of the Board for Da Volterra, a French privately held company, since December 2021. From 2016 to 2021, Mr. Baluch served as the Chief Executive Officer and Board member of CorMedix, Inc., a publicly traded pharmaceutical company in the US. Mr. Baluch also held various senior positions at UCB, S.A. between January 2008 to April 2016, including Senior Vice President and President Europe, Middle East & Africa. Prior to joining UCB, Mr. Baluch worked for Eli Lilly and Company for 24 years, holding international positions spanning Europe, the Middle East and the United States in general management, business development, market access and product leadership. Mr. Baluch holds a B.S. in Aeronautical Engineering from City University London and an MBA from Cranfield School of Management.
- James Neal
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James Neal,自2022年7月起担任董事。他在全球范围内形成和最大限度地扩大业务和技术合作以及将新颖的产品和技术推向市场方面拥有超过25年的经验。Neal先生自2016年12月起担任XOMA的首席执行官兼董事,直至2023年1月退休。Neal先生于2009年加入XOMA,担任业务发展副总裁。在加入XOMA之前,Neal先生是领先的生物模拟公司Entelos,Inc.的代理首席执行官。在此之前的2007年,Entelos收购了Iconix Biosciences,这是一家私人控股公司,Neal先生担任首席执行官,并与百时美施贵宝、雅培实验室、礼来和美国食品药品监督管理局建立了多年合作关系。1999年至2002年担任因塞特医疗基因组学执行副总裁期间,他领导了与制药公司合作者和合作伙伴的全球商业活动,包括辉瑞、安万特和Schering-Plough,以及公司的销售、市场营销和业务发展活动。早些时候,他与孟山都公司有关联,担任的职务越来越重。Neal先生还担任临床阶段生物制药公司Palisade Bio, Inc.和特殊目的收购公司Monterey Bio的董事会成员。Neal先生在加拿大马尼托巴大学获得生物学学士学位和遗传学和植物育种硕士学位,并拥有密苏里州圣路易斯华盛顿大学的高级管理人员MBA学位。
James Neal,has served as a Director since July 2022. He brings more than 25 years of experience forming and maximizing business and technology collaborations globally and in bringing novel products and technologies to market. Mr. Neal served as the Chief Executive Officer and Director of XOMA from December 2016 until his retirement in January 2023. Mr. Neal joined XOMA in 2009 as its Vice President, Business Development. Prior to joining XOMA, Mr. Neal was Acting Chief Executive Officer of Entelos, Inc. a leading biosimulation company. Previously, in 2007, Entelos acquired Iconix Biosciences, a privately held company where Mr. Neal served as Chief Executive Officer and established multi-year collaborations with Bristol-Myers Squibb, Abbott Labs, Eli Lilly and the U.S. Food and Drug Administration. While Executive Vice President of Incyte Genomics from 1999 to 2002, he led the global commercial activities with pharmaceutical company collaborators and partners including Pfizer, Aventis and Schering-Plough, as well as sales, marketing and business development activities for the company. Earlier, he was associated with Monsanto Company in positions of increasing responsibility. Mr. Neal also serves on the Board of Directors of Palisade Bio, Inc., a clinical-stage biopharmaceutical company, and Monterey Bio, a special purpose acquisition company. Mr. Neal earned his B.S. in Biology and his M.S. in Genetics and Plant Breeding from the University of Manitoba, Canada, and holds an Executive MBA degree from Washington University in St. Louis, Missouri. - James Neal,自2022年7月起担任董事。他在全球范围内形成和最大限度地扩大业务和技术合作以及将新颖的产品和技术推向市场方面拥有超过25年的经验。Neal先生自2016年12月起担任XOMA的首席执行官兼董事,直至2023年1月退休。Neal先生于2009年加入XOMA,担任业务发展副总裁。在加入XOMA之前,Neal先生是领先的生物模拟公司Entelos,Inc.的代理首席执行官。在此之前的2007年,Entelos收购了Iconix Biosciences,这是一家私人控股公司,Neal先生担任首席执行官,并与百时美施贵宝、雅培实验室、礼来和美国食品药品监督管理局建立了多年合作关系。1999年至2002年担任因塞特医疗基因组学执行副总裁期间,他领导了与制药公司合作者和合作伙伴的全球商业活动,包括辉瑞、安万特和Schering-Plough,以及公司的销售、市场营销和业务发展活动。早些时候,他与孟山都公司有关联,担任的职务越来越重。Neal先生还担任临床阶段生物制药公司Palisade Bio, Inc.和特殊目的收购公司Monterey Bio的董事会成员。Neal先生在加拿大马尼托巴大学获得生物学学士学位和遗传学和植物育种硕士学位,并拥有密苏里州圣路易斯华盛顿大学的高级管理人员MBA学位。
- James Neal,has served as a Director since July 2022. He brings more than 25 years of experience forming and maximizing business and technology collaborations globally and in bringing novel products and technologies to market. Mr. Neal served as the Chief Executive Officer and Director of XOMA from December 2016 until his retirement in January 2023. Mr. Neal joined XOMA in 2009 as its Vice President, Business Development. Prior to joining XOMA, Mr. Neal was Acting Chief Executive Officer of Entelos, Inc. a leading biosimulation company. Previously, in 2007, Entelos acquired Iconix Biosciences, a privately held company where Mr. Neal served as Chief Executive Officer and established multi-year collaborations with Bristol-Myers Squibb, Abbott Labs, Eli Lilly and the U.S. Food and Drug Administration. While Executive Vice President of Incyte Genomics from 1999 to 2002, he led the global commercial activities with pharmaceutical company collaborators and partners including Pfizer, Aventis and Schering-Plough, as well as sales, marketing and business development activities for the company. Earlier, he was associated with Monsanto Company in positions of increasing responsibility. Mr. Neal also serves on the Board of Directors of Palisade Bio, Inc., a clinical-stage biopharmaceutical company, and Monterey Bio, a special purpose acquisition company. Mr. Neal earned his B.S. in Biology and his M.S. in Genetics and Plant Breeding from the University of Manitoba, Canada, and holds an Executive MBA degree from Washington University in St. Louis, Missouri.
- Virgil Thompson
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Virgil Thompson,Thompson自1994年起担任董事;公司提名和公司治理委员会主席,审计和财务委员会成员。Thompson自2009年7月起担任Spinnaker Biosciences, Inc.(一家私人眼科药物输送公司)首席执行官。Thompson从2002年到2007年7月担任Angstrom Pharmaceuticals, Inc.(一家制药公司)总裁和首席执行官,并担任其董事一直到2009年。Thompson从2000年到2002年担任Chimeric Therapies, Inc.(一家生物制药公司)总裁、首席执行官和董事;1999年到2000年担任其总裁和首席运营官。1996年到1999年Thompson担任Cytel Corporation(一家生物制药公司)总裁和首席执行官。Thompson是Aradigm Corporation(一家新兴专业制药公司)董事长,薪酬、提名和企业管制、审计委员会成员。Thompson是Questcor Pharmaceuticals, Inc.(一家生物制药公司)董事长,并担任起薪酬、合规和审计委员会成员。
Virgil Thompson,has served as a Director since October 2017 and previously served on the Board of Directors at Promet Therapeutics, LLC. He also served as a Director of Mallinckrodt Pharmaceuticals (formerly Questcor Pharmaceuticals) and as a Director of GenZ Corporation; he resigned from both companies in 2017. From July 2009 to July 2015, he served as Chief Executive Officer and Director of Spinnaker Biosciences, Inc., and now serves as Chairman of the Board. Mr. Thompson also served as Chairman of the Board of Aradigm Corporation, as well as of Questcor Pharmaceuticals, Inc. until Questcor was acquired by Mallinckrodt in August 2014. Mr. Thompson served as the Chief Executive Officer and as a Director of Angstrom Pharmaceuticals, Inc. from 2002 to 2007. From 2000 to 2002, Mr. Thompson was Chief Executive Officer and a Director of Chimeric Therapies, Inc. From 1999 to 2000, Mr. Thompson was President, Chief Operating Officer and, from 1994, a Director of Bio-Technology General Corporation (subsequently Savient Pharmaceuticals, Inc.). Mr. Thompson obtained a B.S. in Pharmacy from the University of Kansas and a J.D. degree from the George Washington University Law School. - Virgil Thompson,Thompson自1994年起担任董事;公司提名和公司治理委员会主席,审计和财务委员会成员。Thompson自2009年7月起担任Spinnaker Biosciences, Inc.(一家私人眼科药物输送公司)首席执行官。Thompson从2002年到2007年7月担任Angstrom Pharmaceuticals, Inc.(一家制药公司)总裁和首席执行官,并担任其董事一直到2009年。Thompson从2000年到2002年担任Chimeric Therapies, Inc.(一家生物制药公司)总裁、首席执行官和董事;1999年到2000年担任其总裁和首席运营官。1996年到1999年Thompson担任Cytel Corporation(一家生物制药公司)总裁和首席执行官。Thompson是Aradigm Corporation(一家新兴专业制药公司)董事长,薪酬、提名和企业管制、审计委员会成员。Thompson是Questcor Pharmaceuticals, Inc.(一家生物制药公司)董事长,并担任起薪酬、合规和审计委员会成员。
- Virgil Thompson,has served as a Director since October 2017 and previously served on the Board of Directors at Promet Therapeutics, LLC. He also served as a Director of Mallinckrodt Pharmaceuticals (formerly Questcor Pharmaceuticals) and as a Director of GenZ Corporation; he resigned from both companies in 2017. From July 2009 to July 2015, he served as Chief Executive Officer and Director of Spinnaker Biosciences, Inc., and now serves as Chairman of the Board. Mr. Thompson also served as Chairman of the Board of Aradigm Corporation, as well as of Questcor Pharmaceuticals, Inc. until Questcor was acquired by Mallinckrodt in August 2014. Mr. Thompson served as the Chief Executive Officer and as a Director of Angstrom Pharmaceuticals, Inc. from 2002 to 2007. From 2000 to 2002, Mr. Thompson was Chief Executive Officer and a Director of Chimeric Therapies, Inc. From 1999 to 2000, Mr. Thompson was President, Chief Operating Officer and, from 1994, a Director of Bio-Technology General Corporation (subsequently Savient Pharmaceuticals, Inc.). Mr. Thompson obtained a B.S. in Pharmacy from the University of Kansas and a J.D. degree from the George Washington University Law School.
- David Young
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David Young,他是博士。他于2006年9月加入Processa Pharmaceuticals, Inc.的董事会,担任首席科学官。他于2009年10月被任命为首席科学官。担任Questcor公司执行官之前,他曾担任Processa Pharmaceuticals, Inc.董事会成员(从2006年9月到他退休)。他曾担任AGI Therapeutics公司的总裁(从2006年到2009年)。此前,他曾担任ICON公司(一个国际化合同研究组织(CRO))的战略药物开发部门的执行副总裁(从2003年到2006年),以及GloboMax公司(ICON公司于2003年收购的合同药物开发公司)的创始人兼首席执行官(从1997年到2003年)。创立GloboMax公司之前,他曾担任University of Maryland的药剂学院的副教授,在那里他曾担任一系列职务,包括药物动力学和生物药剂学实验室的董事、the University of Maryland-VA Clinical Research Unit的董事总经理。他持有加州大学伯克利分校(the Fisher Center Policy Advisory Board)的生理学学士学位、威斯康星大学麦迪逊分校(the University of Wisconsin - Madison)的医学物理学硕士学位、南加利福尼亚大学(the University of Southern California)的药学博士学位,以及the University of Southern California的制药科学博士学位。
David Young,has served as Processa Pharmaceuticals, Inc. Chief Executive Officer since October 4, 2017 and has over 30 years of pharmaceutical research, drug development and corporate experience. He also served as Processa Pharmaceuticals, Inc. Chairman until July 11, 2022, at which point he became Processa Pharmaceuticals, Inc. President. Additionally, he served as Processa Pharmaceuticals, Inc. interim CFO from October 4, 2017 to September 1, 2018. From 2006 to 2009, prior to joining the Questcor executive management team, Dr. Young served as an independent Director on the Questcor Board of Directors. As an independent director, Dr. Young, representing Questcor, worked with the FDA in developing a process to obtain approval for Acthar (the only commercial product owned by Questcor) in Infantile Spasms (IS), a deadly and debilitating very rare orphan indication. In 2009, Dr. Young joined the Questcor executive management team as Chief Scientific Officer (CSO) in order to obtain IS FDA approval and market exclusivity by completing the New Drug Application (NDA) process, working with FDA on modernizing the label, and leading all aspects of approval including the Advisory Committee Meeting that voted to approve the NDA for IS. During the eight years that Dr. Young was involved with Questcor as an independent director and as its CSO, Questcor transitioned to an orphan drug specialty pharmaceutical company, moving from an outdated Acthar label and near bankruptcy in 2007 to a modernized Acthar label that helped it to achieve sales greater than $750 million per year and the ultimate sale of the company for approximately $5.6 billion in 2014. While serving on Questcor's Board of Directors, Dr. Young was Executive Director & President, U.S. Operations of AGI Therapeutics plc. Dr. Young has also served as the Executive Vice President of the Strategic Drug Development Division of ICON plc, an international CRO, and was the Founder and CEO of GloboMax LLC, a CRO specializing in FDA drug development, which was purchased by ICON plc in 2003. Prior to forming GloboMax, Dr. Young was a Tenured Associate Professor at the School of Pharmacy, University of Maryland at Baltimore (UMAB), where he led a group of 30 faculty, scientists, postdocs, graduate students and technicians in evaluating the biological properties of drugs and drug delivery systems in animals and humans.Dr. Young is an expert in small molecule and protein non-clinical and clinical drug development. He has served on FDA Advisory Committees, was Co-Principal Investigator on an FDA-funded Clinical Pharmacology contract, was responsible for the analytical and pharmacokinetic evaluation of all oral products manufactured in the UMAB-FDA contract which led to the Scale-up and Post-Approval Changes (SUPAC) and in-vitro in-vivo correlation (IVIVC) FDA Guidance, taught FDA reviewers as part of the UMAB-FDA contract for five years, has served on National Institutes of Health (NIH) grant review committees, and was Co-Principal Investigator on a National Cancer Institute contract to evaluate new oncology drugs. Dr. Young has met with the FDA over 100 times on more than 50 drug products and has been a key team member on more than 30 NDA/supplemental NDA approvals. Dr. Young has more than 150 presentations-authored publications-book chapters, including formal presentations to the FDA, FDA Advisory Committees, and numerous invited presentations at both scientific and investment meetings. Dr. Young received his B.S. in Physiology from the University of California at Berkeley, his M.S. in Medical Physics from the University of Wisconsin at Madison, and his Pharm.D. - Ph.D. with emphasis in Pharmacokinetics and Pharmaceutical Sciences from the University of Southern California. - David Young,他是博士。他于2006年9月加入Processa Pharmaceuticals, Inc.的董事会,担任首席科学官。他于2009年10月被任命为首席科学官。担任Questcor公司执行官之前,他曾担任Processa Pharmaceuticals, Inc.董事会成员(从2006年9月到他退休)。他曾担任AGI Therapeutics公司的总裁(从2006年到2009年)。此前,他曾担任ICON公司(一个国际化合同研究组织(CRO))的战略药物开发部门的执行副总裁(从2003年到2006年),以及GloboMax公司(ICON公司于2003年收购的合同药物开发公司)的创始人兼首席执行官(从1997年到2003年)。创立GloboMax公司之前,他曾担任University of Maryland的药剂学院的副教授,在那里他曾担任一系列职务,包括药物动力学和生物药剂学实验室的董事、the University of Maryland-VA Clinical Research Unit的董事总经理。他持有加州大学伯克利分校(the Fisher Center Policy Advisory Board)的生理学学士学位、威斯康星大学麦迪逊分校(the University of Wisconsin - Madison)的医学物理学硕士学位、南加利福尼亚大学(the University of Southern California)的药学博士学位,以及the University of Southern California的制药科学博士学位。
- David Young,has served as Processa Pharmaceuticals, Inc. Chief Executive Officer since October 4, 2017 and has over 30 years of pharmaceutical research, drug development and corporate experience. He also served as Processa Pharmaceuticals, Inc. Chairman until July 11, 2022, at which point he became Processa Pharmaceuticals, Inc. President. Additionally, he served as Processa Pharmaceuticals, Inc. interim CFO from October 4, 2017 to September 1, 2018. From 2006 to 2009, prior to joining the Questcor executive management team, Dr. Young served as an independent Director on the Questcor Board of Directors. As an independent director, Dr. Young, representing Questcor, worked with the FDA in developing a process to obtain approval for Acthar (the only commercial product owned by Questcor) in Infantile Spasms (IS), a deadly and debilitating very rare orphan indication. In 2009, Dr. Young joined the Questcor executive management team as Chief Scientific Officer (CSO) in order to obtain IS FDA approval and market exclusivity by completing the New Drug Application (NDA) process, working with FDA on modernizing the label, and leading all aspects of approval including the Advisory Committee Meeting that voted to approve the NDA for IS. During the eight years that Dr. Young was involved with Questcor as an independent director and as its CSO, Questcor transitioned to an orphan drug specialty pharmaceutical company, moving from an outdated Acthar label and near bankruptcy in 2007 to a modernized Acthar label that helped it to achieve sales greater than $750 million per year and the ultimate sale of the company for approximately $5.6 billion in 2014. While serving on Questcor's Board of Directors, Dr. Young was Executive Director & President, U.S. Operations of AGI Therapeutics plc. Dr. Young has also served as the Executive Vice President of the Strategic Drug Development Division of ICON plc, an international CRO, and was the Founder and CEO of GloboMax LLC, a CRO specializing in FDA drug development, which was purchased by ICON plc in 2003. Prior to forming GloboMax, Dr. Young was a Tenured Associate Professor at the School of Pharmacy, University of Maryland at Baltimore (UMAB), where he led a group of 30 faculty, scientists, postdocs, graduate students and technicians in evaluating the biological properties of drugs and drug delivery systems in animals and humans.Dr. Young is an expert in small molecule and protein non-clinical and clinical drug development. He has served on FDA Advisory Committees, was Co-Principal Investigator on an FDA-funded Clinical Pharmacology contract, was responsible for the analytical and pharmacokinetic evaluation of all oral products manufactured in the UMAB-FDA contract which led to the Scale-up and Post-Approval Changes (SUPAC) and in-vitro in-vivo correlation (IVIVC) FDA Guidance, taught FDA reviewers as part of the UMAB-FDA contract for five years, has served on National Institutes of Health (NIH) grant review committees, and was Co-Principal Investigator on a National Cancer Institute contract to evaluate new oncology drugs. Dr. Young has met with the FDA over 100 times on more than 50 drug products and has been a key team member on more than 30 NDA/supplemental NDA approvals. Dr. Young has more than 150 presentations-authored publications-book chapters, including formal presentations to the FDA, FDA Advisory Committees, and numerous invited presentations at both scientific and investment meetings. Dr. Young received his B.S. in Physiology from the University of California at Berkeley, his M.S. in Medical Physics from the University of Wisconsin at Madison, and his Pharm.D. - Ph.D. with emphasis in Pharmacokinetics and Pharmaceutical Sciences from the University of Southern California.
高管简历
中英对照 |  中文 |  英文- Patrick Lin
Patrick Lin自2017年10月4日起担任我们的首席业务和战略官。他曾是Promet Therapeutics,LLC的联合创始人和董事会主席。他是Primarius Capital公司(家族办公室,管理专注于小型资本公司的公共和私人投资)的创始人,并担任其管理合伙人15年以上。在成立Primarius Capital之前的10年里,Lin先生在多家华尔街银行和经纪公司任职,包括Robertson Stephens&Co.,E*Offering和Goldman Sachs&Co.。林先生是E*Offering的联合创始合伙人。Lin先生在凯洛格管理研究生院(Kellogg Graduate School of Management)获得工商管理硕士学位,并在南加州大学(University of Southern California)获得工商管理理学学士学位。
Patrick Lin,has served as Processa Pharmaceuticals, Inc. Chief Business & Strategy Officer since October 4, 2017 and has over 20 years of financing and investing experience in the Biopharm Sector. He is founder and, for more than 15 years, Managing Partner of Primarius Capital, a family office that manages public and private investments focused on small capitalization companies. For 10 years prior to forming Primarius Capital, Mr. Lin worked at several Wall Street banking and brokerage firms including Robertson Stephens & Co., E*Offering, and Goldman Sachs & Co. Mr. Lin was Co-Founding Partner of E*Offering. Mr. Lin received an MBA from Kellogg Graduate School of Management, an M.S. in Engineering Management, and a BSBA from the University of Southern California.- Patrick Lin自2017年10月4日起担任我们的首席业务和战略官。他曾是Promet Therapeutics,LLC的联合创始人和董事会主席。他是Primarius Capital公司(家族办公室,管理专注于小型资本公司的公共和私人投资)的创始人,并担任其管理合伙人15年以上。在成立Primarius Capital之前的10年里,Lin先生在多家华尔街银行和经纪公司任职,包括Robertson Stephens&Co.,E*Offering和Goldman Sachs&Co.。林先生是E*Offering的联合创始合伙人。Lin先生在凯洛格管理研究生院(Kellogg Graduate School of Management)获得工商管理硕士学位,并在南加州大学(University of Southern California)获得工商管理理学学士学位。
- Patrick Lin,has served as Processa Pharmaceuticals, Inc. Chief Business & Strategy Officer since October 4, 2017 and has over 20 years of financing and investing experience in the Biopharm Sector. He is founder and, for more than 15 years, Managing Partner of Primarius Capital, a family office that manages public and private investments focused on small capitalization companies. For 10 years prior to forming Primarius Capital, Mr. Lin worked at several Wall Street banking and brokerage firms including Robertson Stephens & Co., E*Offering, and Goldman Sachs & Co. Mr. Lin was Co-Founding Partner of E*Offering. Mr. Lin received an MBA from Kellogg Graduate School of Management, an M.S. in Engineering Management, and a BSBA from the University of Southern California.
- Sian Bigora
Sian Bigora自2017年10月4日起担任我们的首席开发官。她曾是Promet Therapeutics,LLC的联合创始人、董事和首席发展官。任职ProMet公司之前,Bigora博士曾担任Questcor Pharmaceuticals公司的监管事务Vice President,该公司于2014年被Mallinckrodt Pharmaceuticals公司收购(2009年至2015年),包括领导Acthar凝胶标签的现代化工作,以及获得FDA批准治疗婴儿痉挛,这些事件对Questcor公司随后的成功至关重要。任职Questcor公司期间,她曾协助建立一个专家监管小组,以解决Acthar公司等复杂产品的商业和开发需求。Bigora博士在Questcor的职责包括领导安全药物警戒小组和临床质量小组的开发。在Questcor任职之前,Bigora博士是AGI Therapeutics,plc.美国业务临床和监管事务的Vice President。担任该职位时,她负责全球3期研究的开发和实施以及与监管机构的互动。此前,她运营自己的咨询公司,担任多个中小型制药公司的监管和药物开发专家团队成员。Bigora博士在监管事务,运营和项目管理方面担任多个职位,最后担任Icon,plc(一家国际CRO)的战略药物开发部门的监管事务副总裁,以及Globomax LLC(一家专注于FDA药物开发的CRO,于2003年被Icon plc收购)的监管事务副总裁。任职Globomax公司之前,她曾任职the School of Pharmaceuticals,University of Maryland的药物动力学和生物制药实验室,涉及FDA资助的临床药理合同和Umab-FDA合同,担任FDA审查员的临床科学家和导师。Bigora医生拿到了药检报告来自巴尔的摩的马里兰大学药学院。她还在马里兰大学巴尔的摩分校(University of Maryland at Baltimore)完成了药代动力学和儿科传染病的研究金。
Sian Bigora,has served as Processa Pharmaceuticals, Inc. Chief Development Officer since October 4, 2017 and has over 20 years of pharmaceutical research, regulatory strategy and drug development experience working closely with Dr. Young. From 2009 to 2015 Dr. Bigora was Vice President of Regulatory Affairs at Questcor Pharmaceuticals (acquired by Mallinckrodt Pharmaceuticals in 2014), including leading efforts on modernizing the Acthar Gel label and in obtaining FDA approval in Infantile Spasms, events of material importance to Questcor's subsequent success. During her time at Questcor, she assisted in building an expert regulatory group to address both commercial and development needs for complex products such as Acthar. Dr. Bigora's role at Questcor included heading up the development of a safety pharmacovigilance group and a clinical quality group. Prior to her position at Questcor, Dr. Bigora was Vice President of Clinical and Regulatory Affairs, U.S. Operations of AGI Therapeutics, plc. In this role, she was responsible for the development and implementation of Global Phase 3 studies and interactions with regulatory authorities. Previously, she operated her own consulting company, serving as the regulatory and drug development expert team member for multiple small and mid-sized pharmaceutical companies. Dr. Bigora held multiple positions in regulatory affairs, operations and project management ending as VP of Regulatory Affairs at the Strategic Drug Development Division of ICON, plc, an international CRO, and at GloboMax LLC, a CRO specializing in FDA drug development, purchased by ICON plc in 2003. Prior to GloboMax, she worked in the Pharmacokinetics and Biopharmaceutics Laboratory at the School of Pharmacy, University of Maryland on the FDA funded Clinical Pharmacology contract and UMAB-FDA contract as a clinical scientist and instructor for FDA reviewers. Dr. Bigora received a Pharm.D. from the School of Pharmacy at the University of Maryland at Baltimore. She also completed a Fellowship in Pharmacokinetics and Pediatric Infectious Diseases at the University of Maryland at Baltimore.- Sian Bigora自2017年10月4日起担任我们的首席开发官。她曾是Promet Therapeutics,LLC的联合创始人、董事和首席发展官。任职ProMet公司之前,Bigora博士曾担任Questcor Pharmaceuticals公司的监管事务Vice President,该公司于2014年被Mallinckrodt Pharmaceuticals公司收购(2009年至2015年),包括领导Acthar凝胶标签的现代化工作,以及获得FDA批准治疗婴儿痉挛,这些事件对Questcor公司随后的成功至关重要。任职Questcor公司期间,她曾协助建立一个专家监管小组,以解决Acthar公司等复杂产品的商业和开发需求。Bigora博士在Questcor的职责包括领导安全药物警戒小组和临床质量小组的开发。在Questcor任职之前,Bigora博士是AGI Therapeutics,plc.美国业务临床和监管事务的Vice President。担任该职位时,她负责全球3期研究的开发和实施以及与监管机构的互动。此前,她运营自己的咨询公司,担任多个中小型制药公司的监管和药物开发专家团队成员。Bigora博士在监管事务,运营和项目管理方面担任多个职位,最后担任Icon,plc(一家国际CRO)的战略药物开发部门的监管事务副总裁,以及Globomax LLC(一家专注于FDA药物开发的CRO,于2003年被Icon plc收购)的监管事务副总裁。任职Globomax公司之前,她曾任职the School of Pharmaceuticals,University of Maryland的药物动力学和生物制药实验室,涉及FDA资助的临床药理合同和Umab-FDA合同,担任FDA审查员的临床科学家和导师。Bigora医生拿到了药检报告来自巴尔的摩的马里兰大学药学院。她还在马里兰大学巴尔的摩分校(University of Maryland at Baltimore)完成了药代动力学和儿科传染病的研究金。
- Sian Bigora,has served as Processa Pharmaceuticals, Inc. Chief Development Officer since October 4, 2017 and has over 20 years of pharmaceutical research, regulatory strategy and drug development experience working closely with Dr. Young. From 2009 to 2015 Dr. Bigora was Vice President of Regulatory Affairs at Questcor Pharmaceuticals (acquired by Mallinckrodt Pharmaceuticals in 2014), including leading efforts on modernizing the Acthar Gel label and in obtaining FDA approval in Infantile Spasms, events of material importance to Questcor's subsequent success. During her time at Questcor, she assisted in building an expert regulatory group to address both commercial and development needs for complex products such as Acthar. Dr. Bigora's role at Questcor included heading up the development of a safety pharmacovigilance group and a clinical quality group. Prior to her position at Questcor, Dr. Bigora was Vice President of Clinical and Regulatory Affairs, U.S. Operations of AGI Therapeutics, plc. In this role, she was responsible for the development and implementation of Global Phase 3 studies and interactions with regulatory authorities. Previously, she operated her own consulting company, serving as the regulatory and drug development expert team member for multiple small and mid-sized pharmaceutical companies. Dr. Bigora held multiple positions in regulatory affairs, operations and project management ending as VP of Regulatory Affairs at the Strategic Drug Development Division of ICON, plc, an international CRO, and at GloboMax LLC, a CRO specializing in FDA drug development, purchased by ICON plc in 2003. Prior to GloboMax, she worked in the Pharmacokinetics and Biopharmaceutics Laboratory at the School of Pharmacy, University of Maryland on the FDA funded Clinical Pharmacology contract and UMAB-FDA contract as a clinical scientist and instructor for FDA reviewers. Dr. Bigora received a Pharm.D. from the School of Pharmacy at the University of Maryland at Baltimore. She also completed a Fellowship in Pharmacokinetics and Pediatric Infectious Diseases at the University of Maryland at Baltimore.
- James Stanker
James Stanker自2018年9月5日起担任我们的首席财务官。他曾一直担任Grant Thornton公司的审计合伙人(从2000年2月到2016年8月退休),担任财务领导职务。他的职责包括管理大西洋海岸市场领地的审计质量。从2009年到2012年,他担任Grant Thornton International的审计质量全球主管。在加入Grant Thornton之前,Stanker先生曾担任纳斯达克上市公司和一家私营生命科学公司的首席财务官。Stanker先生是一名注册会计师。他在圣何塞州立大学获得航空学士学位,在东湾加利福尼亚州立大学获得工商管理硕士学位。他曾担任GSESystems,Inc.的董事会成员和审计委员会主席。Stanker先生还是胡德学院(Hood College)George B.Delaplaine商学院的客座教授。
James Stanker,has served as Processa Pharmaceuticals, Inc. Chief Financial Officer since September 5, 2018. Mr. Stanker has over 30 years of financial and executive leadership experience in the areas of accounting principles and audit standards, regulatory reporting, and fiscal management and strategy. He has served in a financial leadership role as an audit partner at Grant Thornton from February 2000 until his retirement in August 2016 and has served companies in a financial advisory role since that time. His responsibilities included managing the audit quality in the Atlantic Coast Market Territory. From 2009 to 2012, he served as the Global Head of Audit Quality for Grant Thornton International. Mr. Stanker is a Certified Public Accountant (inactive). He has a B.S. in Aeronautics from San Jose State University and an MBA from California State University, East Bay. He currently serves as a director and audit committee chairman for Hesperos, Inc, a private company; and previously served as a director of GSE Systems, Inc. Mr. Stanker is also a visiting professor in the George B. Delaplaine School of Business at Hood College in Maryland.- James Stanker自2018年9月5日起担任我们的首席财务官。他曾一直担任Grant Thornton公司的审计合伙人(从2000年2月到2016年8月退休),担任财务领导职务。他的职责包括管理大西洋海岸市场领地的审计质量。从2009年到2012年,他担任Grant Thornton International的审计质量全球主管。在加入Grant Thornton之前,Stanker先生曾担任纳斯达克上市公司和一家私营生命科学公司的首席财务官。Stanker先生是一名注册会计师。他在圣何塞州立大学获得航空学士学位,在东湾加利福尼亚州立大学获得工商管理硕士学位。他曾担任GSESystems,Inc.的董事会成员和审计委员会主席。Stanker先生还是胡德学院(Hood College)George B.Delaplaine商学院的客座教授。
- James Stanker,has served as Processa Pharmaceuticals, Inc. Chief Financial Officer since September 5, 2018. Mr. Stanker has over 30 years of financial and executive leadership experience in the areas of accounting principles and audit standards, regulatory reporting, and fiscal management and strategy. He has served in a financial leadership role as an audit partner at Grant Thornton from February 2000 until his retirement in August 2016 and has served companies in a financial advisory role since that time. His responsibilities included managing the audit quality in the Atlantic Coast Market Territory. From 2009 to 2012, he served as the Global Head of Audit Quality for Grant Thornton International. Mr. Stanker is a Certified Public Accountant (inactive). He has a B.S. in Aeronautics from San Jose State University and an MBA from California State University, East Bay. He currently serves as a director and audit committee chairman for Hesperos, Inc, a private company; and previously served as a director of GSE Systems, Inc. Mr. Stanker is also a visiting professor in the George B. Delaplaine School of Business at Hood College in Maryland.
- Wendy Guy
Wendy Guy自2017年10月4日起担任我们的首席行政官。在过去的18年里,她与Young博士在企业管理和运营、人力资源和财务方面密切合作。她曾是Promet Therapeutics,LLC的联合创始人、董事、首席行政官。任职Promet公司之前,Guy女士曾任职Questcor Pharmaceuticals公司(于2014年被Mallinckrodt Pharmaceuticals公司收购),担任业务运营高级经理,负责Questcor公司的马里兰州办公室。在Questcor工作的五年中,她建立了一个充满活力的行政和合同团队,将马里兰州的办事处从两名员工发展到略低于100人,并在Questcor任职之前将设施从1200平方英尺扩大到15000平方英尺,Guy女士曾担任AGI Therapeutics,plc.的美国运营高级经理。在这个职位上,她负责公司的日常业务和行政运营。此前,她曾担任Icon公司、Globomax公司、Mercer Management Consulting公司的战略药物开发部门的多种高级职务。Guy女士获得了Mount Wachusett Community College的A.A.。
Wendy Guy,has served as Processa Pharmaceuticals, Inc. Chief Administrative Officer since October 4, 2017 and has more than 20 years of experience in business operations. She has worked closely with Dr. Young in the past in corporate management and operations, human resources, and finance roles. From 2009 to 2014, Ms. Guy was employed at Questcor Pharmaceuticals (acquired by Mallinckrodt Pharmaceuticals in 2014) as Senior Manager, Business Operations in charge of the Maryland Office for Questcor. During the five years she spent at Questcor, she built a dynamic administrative and contracts team, grew the Maryland Office from two employees to just under 100, and expanded the facility from 1,200 sq. ft. to 15,000 sq. ft. Prior to her position at Questcor, Ms. Guy was Senior Manager, U.S. Operations of AGI Therapeutics, plc. In this role, she was responsible for the day-to-day business and administrative operations of the company. Previously, she held multiple senior level positions with the Strategic Drug Development Division of ICON, GloboMax, and Mercer Management Consulting. Ms. Guy received an A.A. from Mount Wachusett Community College.- Wendy Guy自2017年10月4日起担任我们的首席行政官。在过去的18年里,她与Young博士在企业管理和运营、人力资源和财务方面密切合作。她曾是Promet Therapeutics,LLC的联合创始人、董事、首席行政官。任职Promet公司之前,Guy女士曾任职Questcor Pharmaceuticals公司(于2014年被Mallinckrodt Pharmaceuticals公司收购),担任业务运营高级经理,负责Questcor公司的马里兰州办公室。在Questcor工作的五年中,她建立了一个充满活力的行政和合同团队,将马里兰州的办事处从两名员工发展到略低于100人,并在Questcor任职之前将设施从1200平方英尺扩大到15000平方英尺,Guy女士曾担任AGI Therapeutics,plc.的美国运营高级经理。在这个职位上,她负责公司的日常业务和行政运营。此前,她曾担任Icon公司、Globomax公司、Mercer Management Consulting公司的战略药物开发部门的多种高级职务。Guy女士获得了Mount Wachusett Community College的A.A.。
- Wendy Guy,has served as Processa Pharmaceuticals, Inc. Chief Administrative Officer since October 4, 2017 and has more than 20 years of experience in business operations. She has worked closely with Dr. Young in the past in corporate management and operations, human resources, and finance roles. From 2009 to 2014, Ms. Guy was employed at Questcor Pharmaceuticals (acquired by Mallinckrodt Pharmaceuticals in 2014) as Senior Manager, Business Operations in charge of the Maryland Office for Questcor. During the five years she spent at Questcor, she built a dynamic administrative and contracts team, grew the Maryland Office from two employees to just under 100, and expanded the facility from 1,200 sq. ft. to 15,000 sq. ft. Prior to her position at Questcor, Ms. Guy was Senior Manager, U.S. Operations of AGI Therapeutics, plc. In this role, she was responsible for the day-to-day business and administrative operations of the company. Previously, she held multiple senior level positions with the Strategic Drug Development Division of ICON, GloboMax, and Mercer Management Consulting. Ms. Guy received an A.A. from Mount Wachusett Community College.
- Michael Floyd
Michael Floyd,自2020年10月6日起担任Processa Pharmaceuticals, Inc.首席运营官。弗洛伊德先生是一位连续创业者,在传染病、肿瘤学和罕见病领域的早期生物制药业务方面拥有超过15年的经验。1996年,他创立了Neurologic,这是一家早期企业,获得了美国国立卫生研究院用于阿尔茨海默病诊断测试的技术许可。弗洛伊德先生是该计划的共同作者,该计划于1998年与杰·洛克菲勒阁下和约翰·霍普金斯大学共同创建了布兰切特·洛克菲勒神经科学研究所。2006年,弗洛伊德先生担任Arpida Ltd.北美子公司的首席执行官,在那里他组织了一种MRSA药物的3期项目并组织了NDA提交。弗洛伊德先生随后领导了美国从2011年开始为Gentium,SPA的去铁布罗肽修复NDA的努力。Floyd先生是Bio-AIM的创始人,该公司正在开发鲍曼不动杆菌的单克隆抗体,也是Exbaq的联合创始人,该公司正在开发革兰氏阴性病原体的疗法。2016年,Floyd先生与他人共同创立了Elion Oncology,并担任其首席执行官,直到加入Processa。Floyd先生获得了乔治敦大学会计学学士学位,是一名注册会计师(非在职)。
Michael Floyd,has served as Processa Pharmaceuticals, Inc. Chief Operating Officer since October 6, 2020. Mr. Floyd has been a serial entrepreneur with over 15 years of experience with early-stage biopharma businesses in infectious diseases, oncology and rare diseases. In 1996, he founded Neurologic, an early-stage enterprise that in-licensed technology from the National Institutes of Health for a diagnostic test for Alzheimer's disease. Mr. Floyd was the co-author of the plan that created the Blanchette Rockefeller Neurosciences Institute in 1998 with the Honorable Jay Rockefeller and Johns Hopkins University. In 2006, Mr. Floyd was the Chief Executive Officer for the North American subsidiary of Arpida Ltd. where he organized the Phase 3 program for an MRSA drug and organized the NDA submission. Mr. Floyd subsequently led the US efforts to remediate the NDA for Gentium, SpA for defibrotide beginning in 2011. Mr. Floyd was the Founder of Bio-AIM, which is developing monoclonal antibodies for Acinetobacter baumannii and a Co-Founder of Exbaq, which is developing therapies for Gram negative pathogens. In 2016, Mr. Floyd co-founded Elion Oncology and served as its Chief Executive Officer until joining Processa. Mr. Floyd received a BSBA in Accounting from Georgetown University and is a Certified Public Accountant (inactive).- Michael Floyd,自2020年10月6日起担任Processa Pharmaceuticals, Inc.首席运营官。弗洛伊德先生是一位连续创业者,在传染病、肿瘤学和罕见病领域的早期生物制药业务方面拥有超过15年的经验。1996年,他创立了Neurologic,这是一家早期企业,获得了美国国立卫生研究院用于阿尔茨海默病诊断测试的技术许可。弗洛伊德先生是该计划的共同作者,该计划于1998年与杰·洛克菲勒阁下和约翰·霍普金斯大学共同创建了布兰切特·洛克菲勒神经科学研究所。2006年,弗洛伊德先生担任Arpida Ltd.北美子公司的首席执行官,在那里他组织了一种MRSA药物的3期项目并组织了NDA提交。弗洛伊德先生随后领导了美国从2011年开始为Gentium,SPA的去铁布罗肽修复NDA的努力。Floyd先生是Bio-AIM的创始人,该公司正在开发鲍曼不动杆菌的单克隆抗体,也是Exbaq的联合创始人,该公司正在开发革兰氏阴性病原体的疗法。2016年,Floyd先生与他人共同创立了Elion Oncology,并担任其首席执行官,直到加入Processa。Floyd先生获得了乔治敦大学会计学学士学位,是一名注册会计师(非在职)。
- Michael Floyd,has served as Processa Pharmaceuticals, Inc. Chief Operating Officer since October 6, 2020. Mr. Floyd has been a serial entrepreneur with over 15 years of experience with early-stage biopharma businesses in infectious diseases, oncology and rare diseases. In 1996, he founded Neurologic, an early-stage enterprise that in-licensed technology from the National Institutes of Health for a diagnostic test for Alzheimer's disease. Mr. Floyd was the co-author of the plan that created the Blanchette Rockefeller Neurosciences Institute in 1998 with the Honorable Jay Rockefeller and Johns Hopkins University. In 2006, Mr. Floyd was the Chief Executive Officer for the North American subsidiary of Arpida Ltd. where he organized the Phase 3 program for an MRSA drug and organized the NDA submission. Mr. Floyd subsequently led the US efforts to remediate the NDA for Gentium, SpA for defibrotide beginning in 2011. Mr. Floyd was the Founder of Bio-AIM, which is developing monoclonal antibodies for Acinetobacter baumannii and a Co-Founder of Exbaq, which is developing therapies for Gram negative pathogens. In 2016, Mr. Floyd co-founded Elion Oncology and served as its Chief Executive Officer until joining Processa. Mr. Floyd received a BSBA in Accounting from Georgetown University and is a Certified Public Accountant (inactive).
- David Young
David Young,他是博士。他于2006年9月加入Processa Pharmaceuticals, Inc.的董事会,担任首席科学官。他于2009年10月被任命为首席科学官。担任Questcor公司执行官之前,他曾担任Processa Pharmaceuticals, Inc.董事会成员(从2006年9月到他退休)。他曾担任AGI Therapeutics公司的总裁(从2006年到2009年)。此前,他曾担任ICON公司(一个国际化合同研究组织(CRO))的战略药物开发部门的执行副总裁(从2003年到2006年),以及GloboMax公司(ICON公司于2003年收购的合同药物开发公司)的创始人兼首席执行官(从1997年到2003年)。创立GloboMax公司之前,他曾担任University of Maryland的药剂学院的副教授,在那里他曾担任一系列职务,包括药物动力学和生物药剂学实验室的董事、the University of Maryland-VA Clinical Research Unit的董事总经理。他持有加州大学伯克利分校(the Fisher Center Policy Advisory Board)的生理学学士学位、威斯康星大学麦迪逊分校(the University of Wisconsin - Madison)的医学物理学硕士学位、南加利福尼亚大学(the University of Southern California)的药学博士学位,以及the University of Southern California的制药科学博士学位。
David Young,has served as Processa Pharmaceuticals, Inc. Chief Executive Officer since October 4, 2017 and has over 30 years of pharmaceutical research, drug development and corporate experience. He also served as Processa Pharmaceuticals, Inc. Chairman until July 11, 2022, at which point he became Processa Pharmaceuticals, Inc. President. Additionally, he served as Processa Pharmaceuticals, Inc. interim CFO from October 4, 2017 to September 1, 2018. From 2006 to 2009, prior to joining the Questcor executive management team, Dr. Young served as an independent Director on the Questcor Board of Directors. As an independent director, Dr. Young, representing Questcor, worked with the FDA in developing a process to obtain approval for Acthar (the only commercial product owned by Questcor) in Infantile Spasms (IS), a deadly and debilitating very rare orphan indication. In 2009, Dr. Young joined the Questcor executive management team as Chief Scientific Officer (CSO) in order to obtain IS FDA approval and market exclusivity by completing the New Drug Application (NDA) process, working with FDA on modernizing the label, and leading all aspects of approval including the Advisory Committee Meeting that voted to approve the NDA for IS. During the eight years that Dr. Young was involved with Questcor as an independent director and as its CSO, Questcor transitioned to an orphan drug specialty pharmaceutical company, moving from an outdated Acthar label and near bankruptcy in 2007 to a modernized Acthar label that helped it to achieve sales greater than $750 million per year and the ultimate sale of the company for approximately $5.6 billion in 2014. While serving on Questcor's Board of Directors, Dr. Young was Executive Director & President, U.S. Operations of AGI Therapeutics plc. Dr. Young has also served as the Executive Vice President of the Strategic Drug Development Division of ICON plc, an international CRO, and was the Founder and CEO of GloboMax LLC, a CRO specializing in FDA drug development, which was purchased by ICON plc in 2003. Prior to forming GloboMax, Dr. Young was a Tenured Associate Professor at the School of Pharmacy, University of Maryland at Baltimore (UMAB), where he led a group of 30 faculty, scientists, postdocs, graduate students and technicians in evaluating the biological properties of drugs and drug delivery systems in animals and humans.Dr. Young is an expert in small molecule and protein non-clinical and clinical drug development. He has served on FDA Advisory Committees, was Co-Principal Investigator on an FDA-funded Clinical Pharmacology contract, was responsible for the analytical and pharmacokinetic evaluation of all oral products manufactured in the UMAB-FDA contract which led to the Scale-up and Post-Approval Changes (SUPAC) and in-vitro in-vivo correlation (IVIVC) FDA Guidance, taught FDA reviewers as part of the UMAB-FDA contract for five years, has served on National Institutes of Health (NIH) grant review committees, and was Co-Principal Investigator on a National Cancer Institute contract to evaluate new oncology drugs. Dr. Young has met with the FDA over 100 times on more than 50 drug products and has been a key team member on more than 30 NDA/supplemental NDA approvals. Dr. Young has more than 150 presentations-authored publications-book chapters, including formal presentations to the FDA, FDA Advisory Committees, and numerous invited presentations at both scientific and investment meetings. Dr. Young received his B.S. in Physiology from the University of California at Berkeley, his M.S. in Medical Physics from the University of Wisconsin at Madison, and his Pharm.D. - Ph.D. with emphasis in Pharmacokinetics and Pharmaceutical Sciences from the University of Southern California.- David Young,他是博士。他于2006年9月加入Processa Pharmaceuticals, Inc.的董事会,担任首席科学官。他于2009年10月被任命为首席科学官。担任Questcor公司执行官之前,他曾担任Processa Pharmaceuticals, Inc.董事会成员(从2006年9月到他退休)。他曾担任AGI Therapeutics公司的总裁(从2006年到2009年)。此前,他曾担任ICON公司(一个国际化合同研究组织(CRO))的战略药物开发部门的执行副总裁(从2003年到2006年),以及GloboMax公司(ICON公司于2003年收购的合同药物开发公司)的创始人兼首席执行官(从1997年到2003年)。创立GloboMax公司之前,他曾担任University of Maryland的药剂学院的副教授,在那里他曾担任一系列职务,包括药物动力学和生物药剂学实验室的董事、the University of Maryland-VA Clinical Research Unit的董事总经理。他持有加州大学伯克利分校(the Fisher Center Policy Advisory Board)的生理学学士学位、威斯康星大学麦迪逊分校(the University of Wisconsin - Madison)的医学物理学硕士学位、南加利福尼亚大学(the University of Southern California)的药学博士学位,以及the University of Southern California的制药科学博士学位。
- David Young,has served as Processa Pharmaceuticals, Inc. Chief Executive Officer since October 4, 2017 and has over 30 years of pharmaceutical research, drug development and corporate experience. He also served as Processa Pharmaceuticals, Inc. Chairman until July 11, 2022, at which point he became Processa Pharmaceuticals, Inc. President. Additionally, he served as Processa Pharmaceuticals, Inc. interim CFO from October 4, 2017 to September 1, 2018. From 2006 to 2009, prior to joining the Questcor executive management team, Dr. Young served as an independent Director on the Questcor Board of Directors. As an independent director, Dr. Young, representing Questcor, worked with the FDA in developing a process to obtain approval for Acthar (the only commercial product owned by Questcor) in Infantile Spasms (IS), a deadly and debilitating very rare orphan indication. In 2009, Dr. Young joined the Questcor executive management team as Chief Scientific Officer (CSO) in order to obtain IS FDA approval and market exclusivity by completing the New Drug Application (NDA) process, working with FDA on modernizing the label, and leading all aspects of approval including the Advisory Committee Meeting that voted to approve the NDA for IS. During the eight years that Dr. Young was involved with Questcor as an independent director and as its CSO, Questcor transitioned to an orphan drug specialty pharmaceutical company, moving from an outdated Acthar label and near bankruptcy in 2007 to a modernized Acthar label that helped it to achieve sales greater than $750 million per year and the ultimate sale of the company for approximately $5.6 billion in 2014. While serving on Questcor's Board of Directors, Dr. Young was Executive Director & President, U.S. Operations of AGI Therapeutics plc. Dr. Young has also served as the Executive Vice President of the Strategic Drug Development Division of ICON plc, an international CRO, and was the Founder and CEO of GloboMax LLC, a CRO specializing in FDA drug development, which was purchased by ICON plc in 2003. Prior to forming GloboMax, Dr. Young was a Tenured Associate Professor at the School of Pharmacy, University of Maryland at Baltimore (UMAB), where he led a group of 30 faculty, scientists, postdocs, graduate students and technicians in evaluating the biological properties of drugs and drug delivery systems in animals and humans.Dr. Young is an expert in small molecule and protein non-clinical and clinical drug development. He has served on FDA Advisory Committees, was Co-Principal Investigator on an FDA-funded Clinical Pharmacology contract, was responsible for the analytical and pharmacokinetic evaluation of all oral products manufactured in the UMAB-FDA contract which led to the Scale-up and Post-Approval Changes (SUPAC) and in-vitro in-vivo correlation (IVIVC) FDA Guidance, taught FDA reviewers as part of the UMAB-FDA contract for five years, has served on National Institutes of Health (NIH) grant review committees, and was Co-Principal Investigator on a National Cancer Institute contract to evaluate new oncology drugs. Dr. Young has met with the FDA over 100 times on more than 50 drug products and has been a key team member on more than 30 NDA/supplemental NDA approvals. Dr. Young has more than 150 presentations-authored publications-book chapters, including formal presentations to the FDA, FDA Advisory Committees, and numerous invited presentations at both scientific and investment meetings. Dr. Young received his B.S. in Physiology from the University of California at Berkeley, his M.S. in Medical Physics from the University of Wisconsin at Madison, and his Pharm.D. - Ph.D. with emphasis in Pharmacokinetics and Pharmaceutical Sciences from the University of Southern California.