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
Andre Choulika Director, Chief Executive Officer and Co-Founder 61 未披露 未持股 2026-03-20
David Sourdive Director, Deputy Chief Executive Officer, Executive Vice President, CMC and Manufacturing 59 未披露 未持股 2026-03-20
Donald A. Bergstrom Independent Director 54 未披露 未持股 2026-03-20
Tyrell Rivers Independent Director 53 未披露 未持股 2026-03-20
Rainer Boehm Independent Director 65 未披露 未持股 2026-03-20
André Muller Independent Director 62 未披露 未持股 2026-03-20
Cécile Chartier Independent Director 59 未披露 未持股 2026-03-20
Marc Dunoyer Independent Director 74 未披露 未持股 2026-03-20
Jean Pierre Garnier Chairman of the Board and Director 78 未披露 未持股 2026-03-20
Laurent Arthaud Independent Director 63 未披露 未持股 2026-03-20

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
Andre Choulika Director, Chief Executive Officer and Co-Founder 61 未披露 未持股 2026-03-20
David Sourdive Director, Deputy Chief Executive Officer, Executive Vice President, CMC and Manufacturing 59 未披露 未持股 2026-03-20
Philippe Duchateau Chief Scientific Officer 63 未披露 未持股 2026-03-20
Marie Bleuenn Terrier General Counsel 44 未披露 未持股 2026-03-20
Stephan Reynier Chief Regulatory & Pharmaceutical Compliance Officer 56 未披露 未持股 2026-03-20
Arthur Stril Chief Business Officer and Chief Financial Officer 37 未披露 未持股 2026-03-20
Steven Doares -- Senior Vice President of US Manufacturing 66 未披露 未持股 2026-03-20
Kyung Nam Wortman Chief Human Resources Officer 56 未披露 未持股 2026-03-20
Adrian Kilcoyne Chief Medical Officer 55 未披露 未持股 2026-03-20

董事简历

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Andre Choulika

Andre Choulika,他是Cellectis公司的创始人之一,并一直担任董事会主席兼首席执行官(2000年以来)。他一直担任Calyxt公司的总裁(2010年8月以来)。从1997年到1999年,他曾担任Boston Children’s Hospital的分子医学部门的博士后研究员,在那里他曾担任用于修改复杂基因组的大范围核酸酶分析和使用先驱。他任职于几家生物技术公司的董事会。他持有the University of Paris VI Pierre et Marie Curie的分子生物学博士学位。此后,他获得哈佛医学院的遗传学系的研究奖学金。他也曾在the HEC (Challenge +)进行管理培训。


Andre Choulika is one of the founders of Cellectis and served as Chief Executive Officer since the Company's inception in 1999. He served as Chairman of board of directors from 2011 to November 2020 and Chairman of the board of directors of Calyxt from August 2010 to July 2020. He is CEO and Chairman of Cellectis, Inc. since December 2014 and Cellectis Biologics, Inc. since January 2019. From 1997 to 1999, Dr. Choulika worked as a post doctoral fellow in the Division of Molecular Medicine at Boston Children's Hospital, where he was one of the inventors of nuclease based genome editing technologies and a pioneer in the analysis and e of meganucleases to modify complex genomes. After receiving his Ph.D. in molecular virology from the University of Paris VI (Pierre et Marie Curie), he completed a research fellowship in the Harvard Medical School Department of Genetics. His management training is from the HEC (Challenge +). Since June 2019, Dr. Choulika served at the board of directors of Institut Pasteur. André Choulika was awarded Chevalier of the Légion d'Honneur in France.
Andre Choulika,他是Cellectis公司的创始人之一,并一直担任董事会主席兼首席执行官(2000年以来)。他一直担任Calyxt公司的总裁(2010年8月以来)。从1997年到1999年,他曾担任Boston Children’s Hospital的分子医学部门的博士后研究员,在那里他曾担任用于修改复杂基因组的大范围核酸酶分析和使用先驱。他任职于几家生物技术公司的董事会。他持有the University of Paris VI Pierre et Marie Curie的分子生物学博士学位。此后,他获得哈佛医学院的遗传学系的研究奖学金。他也曾在the HEC (Challenge +)进行管理培训。
Andre Choulika is one of the founders of Cellectis and served as Chief Executive Officer since the Company's inception in 1999. He served as Chairman of board of directors from 2011 to November 2020 and Chairman of the board of directors of Calyxt from August 2010 to July 2020. He is CEO and Chairman of Cellectis, Inc. since December 2014 and Cellectis Biologics, Inc. since January 2019. From 1997 to 1999, Dr. Choulika worked as a post doctoral fellow in the Division of Molecular Medicine at Boston Children's Hospital, where he was one of the inventors of nuclease based genome editing technologies and a pioneer in the analysis and e of meganucleases to modify complex genomes. After receiving his Ph.D. in molecular virology from the University of Paris VI (Pierre et Marie Curie), he completed a research fellowship in the Harvard Medical School Department of Genetics. His management training is from the HEC (Challenge +). Since June 2019, Dr. Choulika served at the board of directors of Institut Pasteur. André Choulika was awarded Chevalier of the Légion d'Honneur in France.
David Sourdive

David Sourdive是Cellectis公司创始人之一,自2008年以来一直担任执行副总裁的职位,负责企业发展。Sourdive博士也自2000年以来成为我们的董事会的成员。从2009年到2012年他担任Ectycell SAS的总裁,自2012年起,他任职于其监督委员会。2014年2月以来Sourdive博士任职于地中海生命科学研究所董事会。之前他任职于Cellectis AB、Medicen Paris Region和 Seine Saint Denis Avenir董事会。从1998年到2000年,他指导生物技术实验室中心和法国国防部Etudes du Bouchet f。从1997年到1998年Sourdive博士在乔治亚州亚特兰大埃默里大学领先的实验室工作并研究病毒免疫学。他主要研究免疫t细胞记忆。Sourdive博士毕业于cole Polytechnique,Pasteur研究所并获得分子病毒学博士学位。他也在the HEC Challenge +。进行过管理培训。


David Sourdive is a co founder of Cellectis and holds the position of Executive Vice President, CMC and Manufacturing since 2017. Prior to that date, Dr. Sdive served as Executive Vice President, Corporate Development since 2008. Dr. Sdive is also a member of board of directors since 2000. Since June 2023 Dr. Sdive serves on the board of directors of hema.to GmbH, from October 2023, he serves at the board of directors of Aqemia SAS, and from September 2024, he serves on the board of Hephaistos S.A.S. From September 2019 to October 2025, he served on the board of directors of Exeloim S.A.S. From February 2021 to September 2025, he served on the board of directors of Cell Easy S.A.S. From February 2014 to April 2024, he served on the board of directors of Mediterranean Institute for Life Sciences (MEDILS). From 2021 to December 2023, he served on the board of directors of Mablink S.A.S. From December 2018 to December 2021, he served on the board of directors of Enobraq SAS. From October 2017 to May 2020, Dr. Sdive served on the Board of Omics SAS. Before his tenure at Cellectis, Dr. Sdive directed the biotechnologies laboratory of the Centre d'Etudes du Bouchet for the French Ministry of Defense. From 1997 to 1998, Dr. Sdive worked at one of the leading laboratories in viral immunology at Emory University in Atlanta, Georgia. His work there was foced on immunological T cell memory. Dr. Sdive graduated from the école Polytechnique and received his PhD in molecular virology at the Institut Pasteur. He also has management training from the HEC (Challenge +).
David Sourdive是Cellectis公司创始人之一,自2008年以来一直担任执行副总裁的职位,负责企业发展。Sourdive博士也自2000年以来成为我们的董事会的成员。从2009年到2012年他担任Ectycell SAS的总裁,自2012年起,他任职于其监督委员会。2014年2月以来Sourdive博士任职于地中海生命科学研究所董事会。之前他任职于Cellectis AB、Medicen Paris Region和 Seine Saint Denis Avenir董事会。从1998年到2000年,他指导生物技术实验室中心和法国国防部Etudes du Bouchet f。从1997年到1998年Sourdive博士在乔治亚州亚特兰大埃默里大学领先的实验室工作并研究病毒免疫学。他主要研究免疫t细胞记忆。Sourdive博士毕业于cole Polytechnique,Pasteur研究所并获得分子病毒学博士学位。他也在the HEC Challenge +。进行过管理培训。
David Sourdive is a co founder of Cellectis and holds the position of Executive Vice President, CMC and Manufacturing since 2017. Prior to that date, Dr. Sdive served as Executive Vice President, Corporate Development since 2008. Dr. Sdive is also a member of board of directors since 2000. Since June 2023 Dr. Sdive serves on the board of directors of hema.to GmbH, from October 2023, he serves at the board of directors of Aqemia SAS, and from September 2024, he serves on the board of Hephaistos S.A.S. From September 2019 to October 2025, he served on the board of directors of Exeloim S.A.S. From February 2021 to September 2025, he served on the board of directors of Cell Easy S.A.S. From February 2014 to April 2024, he served on the board of directors of Mediterranean Institute for Life Sciences (MEDILS). From 2021 to December 2023, he served on the board of directors of Mablink S.A.S. From December 2018 to December 2021, he served on the board of directors of Enobraq SAS. From October 2017 to May 2020, Dr. Sdive served on the Board of Omics SAS. Before his tenure at Cellectis, Dr. Sdive directed the biotechnologies laboratory of the Centre d'Etudes du Bouchet for the French Ministry of Defense. From 1997 to 1998, Dr. Sdive worked at one of the leading laboratories in viral immunology at Emory University in Atlanta, Georgia. His work there was foced on immunological T cell memory. Dr. Sdive graduated from the école Polytechnique and received his PhD in molecular virology at the Institut Pasteur. He also has management training from the HEC (Challenge +).
Donald A. Bergstrom

DonaldA.Bergstrom自2014年1月以来一直担任我们的首席医疗官。此前,从2010年到2014年,Bergstrom博士担任赛诺菲肿瘤科(Sanofi Oncology)的副Vice President兼转化与实验医学全球主管。任职Sanofi公司之前,Bergstrom博士曾任职Merck Research Labs6年,担任临床分子特征分析、肿瘤学临床研究和实验医学肿瘤学集团的多种职务。Bergstrom博士在约翰霍普金斯大学(Johns Hopkins University)获得文学学士学位,并在华盛顿大学(University of Washington)获得病理学硕士学位和博士学位。


Donald A. Bergstrom serves as a member of board of directors since 2022, after having served as observer of board of directors since November 2021. Dr. Bergstrom, currently serves as President, Research and Development at Relay Therapeutics, Inc., a public clinical stage precision medicines company. Prior to his tenure at Relay Therapeutics, from January 2014 to March 2018, Dr. Bergstrom was Chief Medical Officer at Mersana Therapeutics, where he led the advancement of two products based on Mersana's proprietary antibody drug conjugate platform through non clinical development and into Phase 1 clinical trials. Prior to Mersana, he was Global Head of Translational and Experimental Medicine at Sanofi Oncology. At Sanofi, Dr. Bergstrom held roles of increasing responsibility at Merck Research Laboratories, culminating in his role as Oncology Franchise Lead, Experimental Medicine. From 2021 to June 2024, Dr. Bergstrom has served on the board of directors at Fion Pharmaceuticals, a public biotechnologies company. Dr. Bergstrom holds an M.D. from the University of Washington, Seattle, and a Ph.D. from the Fred Hutchinson Cancer Research Center, where he also completed his post doctoral training. He was a resident in clinical pathology at the University of Washington.
DonaldA.Bergstrom自2014年1月以来一直担任我们的首席医疗官。此前,从2010年到2014年,Bergstrom博士担任赛诺菲肿瘤科(Sanofi Oncology)的副Vice President兼转化与实验医学全球主管。任职Sanofi公司之前,Bergstrom博士曾任职Merck Research Labs6年,担任临床分子特征分析、肿瘤学临床研究和实验医学肿瘤学集团的多种职务。Bergstrom博士在约翰霍普金斯大学(Johns Hopkins University)获得文学学士学位,并在华盛顿大学(University of Washington)获得病理学硕士学位和博士学位。
Donald A. Bergstrom serves as a member of board of directors since 2022, after having served as observer of board of directors since November 2021. Dr. Bergstrom, currently serves as President, Research and Development at Relay Therapeutics, Inc., a public clinical stage precision medicines company. Prior to his tenure at Relay Therapeutics, from January 2014 to March 2018, Dr. Bergstrom was Chief Medical Officer at Mersana Therapeutics, where he led the advancement of two products based on Mersana's proprietary antibody drug conjugate platform through non clinical development and into Phase 1 clinical trials. Prior to Mersana, he was Global Head of Translational and Experimental Medicine at Sanofi Oncology. At Sanofi, Dr. Bergstrom held roles of increasing responsibility at Merck Research Laboratories, culminating in his role as Oncology Franchise Lead, Experimental Medicine. From 2021 to June 2024, Dr. Bergstrom has served on the board of directors at Fion Pharmaceuticals, a public biotechnologies company. Dr. Bergstrom holds an M.D. from the University of Washington, Seattle, and a Ph.D. from the Fred Hutchinson Cancer Research Center, where he also completed his post doctoral training. He was a resident in clinical pathology at the University of Washington.
Tyrell Rivers

Tyrell Rivers自2018年2月以来一直担任我们的董事会成员。Rivers博士是阿斯利康公司(AstraZeneca&8217;)企业发展集团的执行董事,负责战略股权投资、并购和撤资,自2014年以来一直担任该职位。在担任该职位之前,Rivers博士从2009年到2014年在MedImmune Ventures任职,在那里他专门从事生物技术投资,并从2001年到2007年在默克制药公司工作,在那里他担任各种技术和商业职务,责任越来越大。Rivers博士担任ADC Therapeutics SA、Armaron Bio Ltd、Cerapedics,Inc.和Corvidia Therapeutics,Inc.以及之前的G1治疗公司和PhaseBioPharmaceuticals,Inc.的董事。Rivers博士拥有麻省理工学院(Massachusetts Institute of Technology)的化学工程学士学位,得克萨斯大学奥斯汀分校(University of Texas at Austin)的化学工程博士学位,以及纽约大学斯特恩商学院(New York University Stern School of Business)的工商管理硕士学位。


Tyrell Rivers has served as a member of our board of directors since February 2018. Dr. Rivers is an Executive Director within AstraZeneca’s Corporate Development group, having responsibility for strategic equity investments, mergers and acquisitions, and divestments and has held this position since 2014. Prior to this role, Dr. Rivers was at MedImmune Ventures from 2009 until 2014 where he specialized in biotechnology investing, and at Merck & Co., Inc. from 2001 through 2007 where he worked in various technical and business roles of increasing responsibility. Dr. Rivers serves on the board of directors for ADC Therapeutics SA, Armaron Bio Ltd, Cerapedics, Inc., and Corvidia Therapeutics, Inc. and previously G1 Therapeutics, Inc. and PhaseBio Pharmaceuticals, Inc. Dr. Rivers holds a B.S. in Chemical Engineering from the Massachusetts Institute of Technology, a Ph.D. in Chemical Engineering from University of Texas at Austin, and an M.B.A. from the New York University Stern School of Business.
Tyrell Rivers自2018年2月以来一直担任我们的董事会成员。Rivers博士是阿斯利康公司(AstraZeneca&8217;)企业发展集团的执行董事,负责战略股权投资、并购和撤资,自2014年以来一直担任该职位。在担任该职位之前,Rivers博士从2009年到2014年在MedImmune Ventures任职,在那里他专门从事生物技术投资,并从2001年到2007年在默克制药公司工作,在那里他担任各种技术和商业职务,责任越来越大。Rivers博士担任ADC Therapeutics SA、Armaron Bio Ltd、Cerapedics,Inc.和Corvidia Therapeutics,Inc.以及之前的G1治疗公司和PhaseBioPharmaceuticals,Inc.的董事。Rivers博士拥有麻省理工学院(Massachusetts Institute of Technology)的化学工程学士学位,得克萨斯大学奥斯汀分校(University of Texas at Austin)的化学工程博士学位,以及纽约大学斯特恩商学院(New York University Stern School of Business)的工商管理硕士学位。
Tyrell Rivers has served as a member of our board of directors since February 2018. Dr. Rivers is an Executive Director within AstraZeneca’s Corporate Development group, having responsibility for strategic equity investments, mergers and acquisitions, and divestments and has held this position since 2014. Prior to this role, Dr. Rivers was at MedImmune Ventures from 2009 until 2014 where he specialized in biotechnology investing, and at Merck & Co., Inc. from 2001 through 2007 where he worked in various technical and business roles of increasing responsibility. Dr. Rivers serves on the board of directors for ADC Therapeutics SA, Armaron Bio Ltd, Cerapedics, Inc., and Corvidia Therapeutics, Inc. and previously G1 Therapeutics, Inc. and PhaseBio Pharmaceuticals, Inc. Dr. Rivers holds a B.S. in Chemical Engineering from the Massachusetts Institute of Technology, a Ph.D. in Chemical Engineering from University of Texas at Austin, and an M.B.A. from the New York University Stern School of Business.
Rainer Boehm

Rainer Boehm自2017年以来一直担任Cellectis的董事会成员。此外,Boehm先生自2018年起担任Humanigen,Inc.和Nordic Nanovector ASA董事会成员。自2019年以来,他一直担任Biocopy AG的董事会成员。Boehm先生在诺华(Novartis)工作了29年,在市场营销&销售和医疗事务方面建立了自己的职业生涯后,在当地,区域和全球担任各种高级管理职位。他领导所有新兴市场地区以及美国和加拿大,无论是肿瘤学还是制药部门。他最近的职务是Novartis Pharma的全球首席商业和医疗事务官,以及临时首席执行官和部门主管Pharma。Rainer在他的职业生涯中推出并监督了许多品牌的商业化,其中包括Femara,Zometa和Glivec,以及Cosentyx和Entresto。Rainer拥有德国the University of Ulm医学学位,以及法国Schiller University工商管理硕士学位。


Rainer Boehm serves as a member of Cellectis' board of directors since 2017. In addition, Mr. Boehm is the founder and owner of Rainer Boehm GmbH and is currently serving on the board of directors of BioCopy AG since February 2020, and Berlin Cure AG since January 2022. From Septembr 2022 to March 2025, Mr. Boehm served on the board of directors of Omega Therapeutics. From 2018 to 2022, Mr. Boehm served on the board of directors of Nordic Nanoverctor SA, and of Humanigen Inc from 2018 to February 2024. Mr. Boehm spent 29 years at Novartis, working locally, regionally and globally in vario senior management roles, after building his career in Marketing & Sales and Medical Affairs. At Novartis, he led all emerging markets regions as ll as the United States and Canada, either for Oncology or the Pharmaceuticals division. His most recent assignments re Chief Commercial and Medical Affairs Officer globally for Novartis Pharma from 2010 to 2017, as ll as ad interim Chief Executive Officer and Division Head Pharma. Rainer launched and oversaw the commercialization of many brands during his career, amongst them Femara, Zometa and Glivec, as ll as Cosentyx and Entresto. Rainer has a medical degree from the University of Ulm in Germany, and a Master of Biness Administration from Schiller University in France.
Rainer Boehm自2017年以来一直担任Cellectis的董事会成员。此外,Boehm先生自2018年起担任Humanigen,Inc.和Nordic Nanovector ASA董事会成员。自2019年以来,他一直担任Biocopy AG的董事会成员。Boehm先生在诺华(Novartis)工作了29年,在市场营销&销售和医疗事务方面建立了自己的职业生涯后,在当地,区域和全球担任各种高级管理职位。他领导所有新兴市场地区以及美国和加拿大,无论是肿瘤学还是制药部门。他最近的职务是Novartis Pharma的全球首席商业和医疗事务官,以及临时首席执行官和部门主管Pharma。Rainer在他的职业生涯中推出并监督了许多品牌的商业化,其中包括Femara,Zometa和Glivec,以及Cosentyx和Entresto。Rainer拥有德国the University of Ulm医学学位,以及法国Schiller University工商管理硕士学位。
Rainer Boehm serves as a member of Cellectis' board of directors since 2017. In addition, Mr. Boehm is the founder and owner of Rainer Boehm GmbH and is currently serving on the board of directors of BioCopy AG since February 2020, and Berlin Cure AG since January 2022. From Septembr 2022 to March 2025, Mr. Boehm served on the board of directors of Omega Therapeutics. From 2018 to 2022, Mr. Boehm served on the board of directors of Nordic Nanoverctor SA, and of Humanigen Inc from 2018 to February 2024. Mr. Boehm spent 29 years at Novartis, working locally, regionally and globally in vario senior management roles, after building his career in Marketing & Sales and Medical Affairs. At Novartis, he led all emerging markets regions as ll as the United States and Canada, either for Oncology or the Pharmaceuticals division. His most recent assignments re Chief Commercial and Medical Affairs Officer globally for Novartis Pharma from 2010 to 2017, as ll as ad interim Chief Executive Officer and Division Head Pharma. Rainer launched and oversaw the commercialization of many brands during his career, amongst them Femara, Zometa and Glivec, as ll as Cosentyx and Entresto. Rainer has a medical degree from the University of Ulm in Germany, and a Master of Biness Administration from Schiller University in France.
André Muller

Andr é Muller自2025年6月起担任董事会成员。Muller先生自2025年起担任Idorsia Pharmaceuticals Ltd.的董事会顾问和首席执行官,并担任Chiron Investment AG的董事。Muller Previoly先生于2024年6月至2025年6月担任Idorsia Pharmaceuticals Ltd的首席执行官,并于2017年6月至2024年6月担任Idorsia Pharmaceuticals Ltd的首席财务官。Muller先生拥有法国里昂EMLYON Biness School的Biness行政管理硕士学位。


André Muller serves as a member of board of directors since June 2025. Mr. Muller serves as advisor to the board of directors and to the chief executive officer of Idorsia Pharmaceuticals Ltd., since 2025, and as director of Chiron Investment AG. Mr. Muller previoly served as chief executive officer of Idorsia Pharmaceuticals Ltd from June 2024 to June 2025 and was chief financial officer of Idorsia Pharmaceuticals Ltd from June 2017 to June 2024. Mr. Muller holds a master's degree in biness administration from EMLYON Biness School, Lyon, France.
Andr é Muller自2025年6月起担任董事会成员。Muller先生自2025年起担任Idorsia Pharmaceuticals Ltd.的董事会顾问和首席执行官,并担任Chiron Investment AG的董事。Muller Previoly先生于2024年6月至2025年6月担任Idorsia Pharmaceuticals Ltd的首席执行官,并于2017年6月至2024年6月担任Idorsia Pharmaceuticals Ltd的首席财务官。Muller先生拥有法国里昂EMLYON Biness School的Biness行政管理硕士学位。
André Muller serves as a member of board of directors since June 2025. Mr. Muller serves as advisor to the board of directors and to the chief executive officer of Idorsia Pharmaceuticals Ltd., since 2025, and as director of Chiron Investment AG. Mr. Muller previoly served as chief executive officer of Idorsia Pharmaceuticals Ltd from June 2024 to June 2025 and was chief financial officer of Idorsia Pharmaceuticals Ltd from June 2017 to June 2024. Mr. Muller holds a master's degree in biness administration from EMLYON Biness School, Lyon, France.
Cécile Chartier

C é cile Chartier自2023年起担任董事会成员。Chartier博士担任CTRL Therapeutics的科学顾问委员会成员。2022年至2024年12月,她担任NextVivo,Inc.的首席科学官。在任职于NextVivo之前,Chartier博士于2017年至2021年担任Iovance Biotherapeutics Inc.的研究副总裁,在那里她通过研究到早期临床试验,领导了下一代肿瘤浸润淋巴细胞(TIL)疗法的开发。在任职于Iovance Biotherapeutics, Inc.之前,她在OncoMed Pharmaceuticals工作了12年,担任靶点验证高级总监,领导多个抗体治疗项目团队从研发到IND备案。她还曾在Shering(Berlex)和Transgene(法国)工作,专注于基因治疗。Chartier博士还于2022年创立了Chartier Consulting。Chartier博士在法国Strasbg的Louis Pasteur大学获得分子生物学博士学位,并在哈佛医学院完成博士后培训。


Cécile Chartier serves as a member of board of directors since 2023. Dr Chartier serves as at the Scientific Board of Advisors of CTRL Therapeutics. From 2022 until December 2024, she was Chief Scientific Officer at NextVivo, Inc. Prior to her tenure at NextVivo, Dr. Chartier was Vice President of Research at Iovance Biotherapeutics Inc. from 2017 to 2021 where she led the development of next generation of tumor infiltrating lymphocytes (TIL) therapies through research to early stage clinical trials. Prior to her time at Iovance Biotherapeutics, Inc., she spent 12 years at OncoMed Pharmaceuticals, where she served as Senior Director of Target Validation and led multiple antibody therapeutics project teams through Research and Development to IND filing. She also worked at Shering ( Berlex) and Transgene (France), where she focused on gene therapy. Dr. Chartier also founded Chartier Consulting in 2022. Dr Chartier obtained her Ph.D. in molecular biology from the Université Louis Pasteur in Strasbg, France and completed post doctoral training at Harvard Medical School.
C é cile Chartier自2023年起担任董事会成员。Chartier博士担任CTRL Therapeutics的科学顾问委员会成员。2022年至2024年12月,她担任NextVivo,Inc.的首席科学官。在任职于NextVivo之前,Chartier博士于2017年至2021年担任Iovance Biotherapeutics Inc.的研究副总裁,在那里她通过研究到早期临床试验,领导了下一代肿瘤浸润淋巴细胞(TIL)疗法的开发。在任职于Iovance Biotherapeutics, Inc.之前,她在OncoMed Pharmaceuticals工作了12年,担任靶点验证高级总监,领导多个抗体治疗项目团队从研发到IND备案。她还曾在Shering(Berlex)和Transgene(法国)工作,专注于基因治疗。Chartier博士还于2022年创立了Chartier Consulting。Chartier博士在法国Strasbg的Louis Pasteur大学获得分子生物学博士学位,并在哈佛医学院完成博士后培训。
Cécile Chartier serves as a member of board of directors since 2023. Dr Chartier serves as at the Scientific Board of Advisors of CTRL Therapeutics. From 2022 until December 2024, she was Chief Scientific Officer at NextVivo, Inc. Prior to her tenure at NextVivo, Dr. Chartier was Vice President of Research at Iovance Biotherapeutics Inc. from 2017 to 2021 where she led the development of next generation of tumor infiltrating lymphocytes (TIL) therapies through research to early stage clinical trials. Prior to her time at Iovance Biotherapeutics, Inc., she spent 12 years at OncoMed Pharmaceuticals, where she served as Senior Director of Target Validation and led multiple antibody therapeutics project teams through Research and Development to IND filing. She also worked at Shering ( Berlex) and Transgene (France), where she focused on gene therapy. Dr. Chartier also founded Chartier Consulting in 2022. Dr Chartier obtained her Ph.D. in molecular biology from the Université Louis Pasteur in Strasbg, France and completed post doctoral training at Harvard Medical School.
Marc Dunoyer

Marc Dunoyer,Marc于2010年1月被任命为葛兰素史克日本地区的主席,于2010年2月开始领导葛兰素史克罕见疾病业务的研发与商业化。他于1999年加入集团,在这之前,从2000年1月到2008年5月担任日本制药部(Pharmaceuticals Japan)的总裁。他从2008年5月到2010年7月担任亚太地区与日本制药部(Pharmaceuticals Asia Pacific/ Japan)的总裁。


Marc Dunoyer's pharmaceutical career includes periods with Roussel Uclaf, Hoechst Marion Roussel and GSK, which has given him extensive industry experience in: finance and accounting; corporate strategy and planning; research and development; sales and marketing; business reorganisation; and business development. Marc is a qualified accountant and joined AstraZeneca in 2013 serving as Executive Vice-President, Global Product and Portfolio Strategy GPPS from June-October 2013. Previously, he served as Global Head of Rare Diseases at GSK and concurrently Chairman, GSK Japan. He holds an MBA from HEC Paris and a Bachelor of Law degree from Paris University. Marc is a Director of Orchard Therapeutics Plc.
Marc Dunoyer,Marc于2010年1月被任命为葛兰素史克日本地区的主席,于2010年2月开始领导葛兰素史克罕见疾病业务的研发与商业化。他于1999年加入集团,在这之前,从2000年1月到2008年5月担任日本制药部(Pharmaceuticals Japan)的总裁。他从2008年5月到2010年7月担任亚太地区与日本制药部(Pharmaceuticals Asia Pacific/ Japan)的总裁。
Marc Dunoyer's pharmaceutical career includes periods with Roussel Uclaf, Hoechst Marion Roussel and GSK, which has given him extensive industry experience in: finance and accounting; corporate strategy and planning; research and development; sales and marketing; business reorganisation; and business development. Marc is a qualified accountant and joined AstraZeneca in 2013 serving as Executive Vice-President, Global Product and Portfolio Strategy GPPS from June-October 2013. Previously, he served as Global Head of Rare Diseases at GSK and concurrently Chairman, GSK Japan. He holds an MBA from HEC Paris and a Bachelor of Law degree from Paris University. Marc is a Director of Orchard Therapeutics Plc.
Jean Pierre Garnier

Jean Pierre Garnier担任Actelion生物制药有限公司的主席,Advent国际(全球私募股权)的经营合伙人。此前,2008至2010年,他曾担任皮埃尔法布尔SA的首席执行官。2000至2008年担任葛兰素史克公司董事会执行委员和首席执行官。2000年担任史克必成有限公司的行政总裁。从1996年到2000年担任史克必成有限公司董事局执行委员和首席营运官。他也是雷诺汽车公司董事和Cerenis治疗(生物制药发展公司)的主席。 2009年,他获大英帝国颁发的骑士司令员。2007年,他从骑士晋升为法国荣誉军团Officer de la。 2006年,他被Best Practice Institute任命为排名前20位的首席执行官。2010至2011年曾任NormOxys公司董事长,斯坦福大学顾问委员会负责学科生物科学的董事,威尔康乃尔医学院和迪拜国际资本顾问委员会的董事会成员。他是保罗-纽曼基金会的董事会成员。


Jean Pierre Garnier serves as a member and Chairman of board of directors since November 2020. Since September 2024, he has served as chairman of the board of directors of BioAge Labs, Inc. From 2019, Dr. Garnier has served as director of the board of directors of Carrier Global Corp., a public company. From 2016 to 2022, Dr. Garnier has served as director of the board of directors of Radi Therapuetic, and from 2018 to 2022, he served as Chairman of the board of directors of Carmat, a public company based in France. From 2018 to 2020, Dr. Garnier was Chairman of Idorsia, a public bio technology company based in Switzerland and listed on the Swiss Stock Exchange (SIX), which was spun off of Actelion LTD with a billion dollar investment from Johnson & Johnson (J&J). Previo to his tenure at Idorsia, he was Chairman of Actelion Ltd., a Swiss pharmaceuticals and bio technology company, sold for $30 billion to Johnson & Johnson. From 2008 to 2010, Dr. Garnier served as Chief Executive Officer of Pierre Fabre, from 2000 to 2008 he served as Chief Executive Officer and Executive Member of the board of directors of GlaxoSmithKline plc, and in 2000, he was Chief Executive Officer of SmithKline Beecham plc. Dr. Garnier has served as board member of Renault S.A., from 2008 to 2016, United Technologies Corporation from 1997 to 2019, and Max Planck Institute from 2013 to 2019. Dr. Garnier holds an MS in pharmaceutical science and a Ph.D. in pharmacology from the Louis Pasteur University of Strasbg, France. He subsequently earned his MBA at Stanford University, California, as a Fulbright Scholar. He was recently promoted from Chevalier to Officier de la Légion d'Honneur of France.
Jean Pierre Garnier担任Actelion生物制药有限公司的主席,Advent国际(全球私募股权)的经营合伙人。此前,2008至2010年,他曾担任皮埃尔法布尔SA的首席执行官。2000至2008年担任葛兰素史克公司董事会执行委员和首席执行官。2000年担任史克必成有限公司的行政总裁。从1996年到2000年担任史克必成有限公司董事局执行委员和首席营运官。他也是雷诺汽车公司董事和Cerenis治疗(生物制药发展公司)的主席。 2009年,他获大英帝国颁发的骑士司令员。2007年,他从骑士晋升为法国荣誉军团Officer de la。 2006年,他被Best Practice Institute任命为排名前20位的首席执行官。2010至2011年曾任NormOxys公司董事长,斯坦福大学顾问委员会负责学科生物科学的董事,威尔康乃尔医学院和迪拜国际资本顾问委员会的董事会成员。他是保罗-纽曼基金会的董事会成员。
Jean Pierre Garnier serves as a member and Chairman of board of directors since November 2020. Since September 2024, he has served as chairman of the board of directors of BioAge Labs, Inc. From 2019, Dr. Garnier has served as director of the board of directors of Carrier Global Corp., a public company. From 2016 to 2022, Dr. Garnier has served as director of the board of directors of Radi Therapuetic, and from 2018 to 2022, he served as Chairman of the board of directors of Carmat, a public company based in France. From 2018 to 2020, Dr. Garnier was Chairman of Idorsia, a public bio technology company based in Switzerland and listed on the Swiss Stock Exchange (SIX), which was spun off of Actelion LTD with a billion dollar investment from Johnson & Johnson (J&J). Previo to his tenure at Idorsia, he was Chairman of Actelion Ltd., a Swiss pharmaceuticals and bio technology company, sold for $30 billion to Johnson & Johnson. From 2008 to 2010, Dr. Garnier served as Chief Executive Officer of Pierre Fabre, from 2000 to 2008 he served as Chief Executive Officer and Executive Member of the board of directors of GlaxoSmithKline plc, and in 2000, he was Chief Executive Officer of SmithKline Beecham plc. Dr. Garnier has served as board member of Renault S.A., from 2008 to 2016, United Technologies Corporation from 1997 to 2019, and Max Planck Institute from 2013 to 2019. Dr. Garnier holds an MS in pharmaceutical science and a Ph.D. in pharmacology from the Louis Pasteur University of Strasbg, France. He subsequently earned his MBA at Stanford University, California, as a Fulbright Scholar. He was recently promoted from Chevalier to Officier de la Légion d'Honneur of France.
Laurent Arthaud

Laurent Arthaud,2007年4月以来,他成为我们董事会的成员。2006年以来,他担任Bpifrance Investissement(原CDC Entreprises,巴黎的在生物技术领域的投资的私人股本公司)的总合伙人。从2004年到2006年,他曾是Pharmavent Partners(总部在巴黎)的管理合伙人。从1999年到2004年,他管理 Aventis的风险投资活动和管理风险资本基金 F.C.P.R.Genavent。他的事业始于1986年在法国国家统计局(INSEE)然后是the Forecasts Department of the French Ministry of Finances。1995年他加入法国总理 Alain Juppéas的技术顾问内阁管理劳动力和失业问题。他于1997年加入Rhne-Poulenc部门并担任科学委员会秘书长。他是巴里理工学院(the Ecole Polytechnique of Paris)和 Ecole Nationale de la Statistique et de l’Administration Economique的毕业生。


Laurent Arthaud serves as a member of board of directors since 2011. Mr. Arthaud is the Managing Director of Life Sciences and Ecotechnologies for Bpifrance Investissement since 2012. He currently serves on the boards of directors of Kurma Life Sciences, Sparingvision, Aledia, and Enyo Pharma. Mr. Arthaud served at the board of directors of Calyxt from 2020 to May 2023, serving as a director designated by Cellectis. He previoly served at the Calyxt's board of directors from July 2017 to May 2019. From 2018 to 2025, Mr. Arthaud served on the board of directors of Ribogenics, Inc. He served on the board of directors of Adocia from 2009 to 2022. From 2006 to 2012, Mr. Arthaud held the position of Deputy CEO at CDC Entreprises. Since 2009 Mr. Arthaud has also directed InnoBio, an investment fund managed by Bpifrance Investissement as part of the FSI France Investissement program. From 1999 to 2004 he served as Vice President of Aventis Capital, an investment subsidiary of the pharmaceuticals group Aventis, and as President of Pharmavent Partners from 2004 to 2006. Mr. Arthaud is a graduate of the cole Polytechnique and the cole Nationale de Statistique et d'Administration conomique.
Laurent Arthaud,2007年4月以来,他成为我们董事会的成员。2006年以来,他担任Bpifrance Investissement(原CDC Entreprises,巴黎的在生物技术领域的投资的私人股本公司)的总合伙人。从2004年到2006年,他曾是Pharmavent Partners(总部在巴黎)的管理合伙人。从1999年到2004年,他管理 Aventis的风险投资活动和管理风险资本基金 F.C.P.R.Genavent。他的事业始于1986年在法国国家统计局(INSEE)然后是the Forecasts Department of the French Ministry of Finances。1995年他加入法国总理 Alain Juppéas的技术顾问内阁管理劳动力和失业问题。他于1997年加入Rhne-Poulenc部门并担任科学委员会秘书长。他是巴里理工学院(the Ecole Polytechnique of Paris)和 Ecole Nationale de la Statistique et de l’Administration Economique的毕业生。
Laurent Arthaud serves as a member of board of directors since 2011. Mr. Arthaud is the Managing Director of Life Sciences and Ecotechnologies for Bpifrance Investissement since 2012. He currently serves on the boards of directors of Kurma Life Sciences, Sparingvision, Aledia, and Enyo Pharma. Mr. Arthaud served at the board of directors of Calyxt from 2020 to May 2023, serving as a director designated by Cellectis. He previoly served at the Calyxt's board of directors from July 2017 to May 2019. From 2018 to 2025, Mr. Arthaud served on the board of directors of Ribogenics, Inc. He served on the board of directors of Adocia from 2009 to 2022. From 2006 to 2012, Mr. Arthaud held the position of Deputy CEO at CDC Entreprises. Since 2009 Mr. Arthaud has also directed InnoBio, an investment fund managed by Bpifrance Investissement as part of the FSI France Investissement program. From 1999 to 2004 he served as Vice President of Aventis Capital, an investment subsidiary of the pharmaceuticals group Aventis, and as President of Pharmavent Partners from 2004 to 2006. Mr. Arthaud is a graduate of the cole Polytechnique and the cole Nationale de Statistique et d'Administration conomique.

高管简历

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Andre Choulika

Andre Choulika,他是Cellectis公司的创始人之一,并一直担任董事会主席兼首席执行官(2000年以来)。他一直担任Calyxt公司的总裁(2010年8月以来)。从1997年到1999年,他曾担任Boston Children’s Hospital的分子医学部门的博士后研究员,在那里他曾担任用于修改复杂基因组的大范围核酸酶分析和使用先驱。他任职于几家生物技术公司的董事会。他持有the University of Paris VI Pierre et Marie Curie的分子生物学博士学位。此后,他获得哈佛医学院的遗传学系的研究奖学金。他也曾在the HEC (Challenge +)进行管理培训。


Andre Choulika is one of the founders of Cellectis and served as Chief Executive Officer since the Company's inception in 1999. He served as Chairman of board of directors from 2011 to November 2020 and Chairman of the board of directors of Calyxt from August 2010 to July 2020. He is CEO and Chairman of Cellectis, Inc. since December 2014 and Cellectis Biologics, Inc. since January 2019. From 1997 to 1999, Dr. Choulika worked as a post doctoral fellow in the Division of Molecular Medicine at Boston Children's Hospital, where he was one of the inventors of nuclease based genome editing technologies and a pioneer in the analysis and e of meganucleases to modify complex genomes. After receiving his Ph.D. in molecular virology from the University of Paris VI (Pierre et Marie Curie), he completed a research fellowship in the Harvard Medical School Department of Genetics. His management training is from the HEC (Challenge +). Since June 2019, Dr. Choulika served at the board of directors of Institut Pasteur. André Choulika was awarded Chevalier of the Légion d'Honneur in France.
Andre Choulika,他是Cellectis公司的创始人之一,并一直担任董事会主席兼首席执行官(2000年以来)。他一直担任Calyxt公司的总裁(2010年8月以来)。从1997年到1999年,他曾担任Boston Children’s Hospital的分子医学部门的博士后研究员,在那里他曾担任用于修改复杂基因组的大范围核酸酶分析和使用先驱。他任职于几家生物技术公司的董事会。他持有the University of Paris VI Pierre et Marie Curie的分子生物学博士学位。此后,他获得哈佛医学院的遗传学系的研究奖学金。他也曾在the HEC (Challenge +)进行管理培训。
Andre Choulika is one of the founders of Cellectis and served as Chief Executive Officer since the Company's inception in 1999. He served as Chairman of board of directors from 2011 to November 2020 and Chairman of the board of directors of Calyxt from August 2010 to July 2020. He is CEO and Chairman of Cellectis, Inc. since December 2014 and Cellectis Biologics, Inc. since January 2019. From 1997 to 1999, Dr. Choulika worked as a post doctoral fellow in the Division of Molecular Medicine at Boston Children's Hospital, where he was one of the inventors of nuclease based genome editing technologies and a pioneer in the analysis and e of meganucleases to modify complex genomes. After receiving his Ph.D. in molecular virology from the University of Paris VI (Pierre et Marie Curie), he completed a research fellowship in the Harvard Medical School Department of Genetics. His management training is from the HEC (Challenge +). Since June 2019, Dr. Choulika served at the board of directors of Institut Pasteur. André Choulika was awarded Chevalier of the Légion d'Honneur in France.
David Sourdive

David Sourdive是Cellectis公司创始人之一,自2008年以来一直担任执行副总裁的职位,负责企业发展。Sourdive博士也自2000年以来成为我们的董事会的成员。从2009年到2012年他担任Ectycell SAS的总裁,自2012年起,他任职于其监督委员会。2014年2月以来Sourdive博士任职于地中海生命科学研究所董事会。之前他任职于Cellectis AB、Medicen Paris Region和 Seine Saint Denis Avenir董事会。从1998年到2000年,他指导生物技术实验室中心和法国国防部Etudes du Bouchet f。从1997年到1998年Sourdive博士在乔治亚州亚特兰大埃默里大学领先的实验室工作并研究病毒免疫学。他主要研究免疫t细胞记忆。Sourdive博士毕业于cole Polytechnique,Pasteur研究所并获得分子病毒学博士学位。他也在the HEC Challenge +。进行过管理培训。


David Sourdive is a co founder of Cellectis and holds the position of Executive Vice President, CMC and Manufacturing since 2017. Prior to that date, Dr. Sdive served as Executive Vice President, Corporate Development since 2008. Dr. Sdive is also a member of board of directors since 2000. Since June 2023 Dr. Sdive serves on the board of directors of hema.to GmbH, from October 2023, he serves at the board of directors of Aqemia SAS, and from September 2024, he serves on the board of Hephaistos S.A.S. From September 2019 to October 2025, he served on the board of directors of Exeloim S.A.S. From February 2021 to September 2025, he served on the board of directors of Cell Easy S.A.S. From February 2014 to April 2024, he served on the board of directors of Mediterranean Institute for Life Sciences (MEDILS). From 2021 to December 2023, he served on the board of directors of Mablink S.A.S. From December 2018 to December 2021, he served on the board of directors of Enobraq SAS. From October 2017 to May 2020, Dr. Sdive served on the Board of Omics SAS. Before his tenure at Cellectis, Dr. Sdive directed the biotechnologies laboratory of the Centre d'Etudes du Bouchet for the French Ministry of Defense. From 1997 to 1998, Dr. Sdive worked at one of the leading laboratories in viral immunology at Emory University in Atlanta, Georgia. His work there was foced on immunological T cell memory. Dr. Sdive graduated from the école Polytechnique and received his PhD in molecular virology at the Institut Pasteur. He also has management training from the HEC (Challenge +).
David Sourdive是Cellectis公司创始人之一,自2008年以来一直担任执行副总裁的职位,负责企业发展。Sourdive博士也自2000年以来成为我们的董事会的成员。从2009年到2012年他担任Ectycell SAS的总裁,自2012年起,他任职于其监督委员会。2014年2月以来Sourdive博士任职于地中海生命科学研究所董事会。之前他任职于Cellectis AB、Medicen Paris Region和 Seine Saint Denis Avenir董事会。从1998年到2000年,他指导生物技术实验室中心和法国国防部Etudes du Bouchet f。从1997年到1998年Sourdive博士在乔治亚州亚特兰大埃默里大学领先的实验室工作并研究病毒免疫学。他主要研究免疫t细胞记忆。Sourdive博士毕业于cole Polytechnique,Pasteur研究所并获得分子病毒学博士学位。他也在the HEC Challenge +。进行过管理培训。
David Sourdive is a co founder of Cellectis and holds the position of Executive Vice President, CMC and Manufacturing since 2017. Prior to that date, Dr. Sdive served as Executive Vice President, Corporate Development since 2008. Dr. Sdive is also a member of board of directors since 2000. Since June 2023 Dr. Sdive serves on the board of directors of hema.to GmbH, from October 2023, he serves at the board of directors of Aqemia SAS, and from September 2024, he serves on the board of Hephaistos S.A.S. From September 2019 to October 2025, he served on the board of directors of Exeloim S.A.S. From February 2021 to September 2025, he served on the board of directors of Cell Easy S.A.S. From February 2014 to April 2024, he served on the board of directors of Mediterranean Institute for Life Sciences (MEDILS). From 2021 to December 2023, he served on the board of directors of Mablink S.A.S. From December 2018 to December 2021, he served on the board of directors of Enobraq SAS. From October 2017 to May 2020, Dr. Sdive served on the Board of Omics SAS. Before his tenure at Cellectis, Dr. Sdive directed the biotechnologies laboratory of the Centre d'Etudes du Bouchet for the French Ministry of Defense. From 1997 to 1998, Dr. Sdive worked at one of the leading laboratories in viral immunology at Emory University in Atlanta, Georgia. His work there was foced on immunological T cell memory. Dr. Sdive graduated from the école Polytechnique and received his PhD in molecular virology at the Institut Pasteur. He also has management training from the HEC (Challenge +).
Philippe Duchateau

Philippe Duchateau于2001年加入Cellectis负责开发基因组工程领域。1993年在法国Pasteur Lille研究所获得生物化学和分子生物学博士学位之后,从1993年到2001年在金山(美国)加州大学心血管研究所他完成了一个研究奖学金。他是核酸酶和基因工程领域多项专利的合作发明者和50多个科学出版物的合作者,合作编辑一本题为Site-directed Insertion of Transgenes的书。自从2004年以来,作为ellectis研究部门的领导者,他帮助Cellectis技术的发展。自2012年以来Philippe Duchateau一直担任首席科学家。


Philippe Duchateau joined Cellectis in 2001 to pioneer the field of genome engineering and has served as Chief Scientific Officer since 2012. After receiving his Ph.D. in 1993 in biochemistry and molecular biology at the Institut Pasteur (Lille, France), he completed a research fellowship from 1993 to 2001 at the University of California, San Francisco (United States) within the Cardiovascular Research Institute. He is co inventor of numero patents in the field of nucleases and genome engineering and co author on more than 50 scientific publications and co editor of one book entitled "Site directed Insertion of Transgenes." As head of Cellectis's Research department since 2004, he helped to the development of the key Cellectis technologies.
Philippe Duchateau于2001年加入Cellectis负责开发基因组工程领域。1993年在法国Pasteur Lille研究所获得生物化学和分子生物学博士学位之后,从1993年到2001年在金山(美国)加州大学心血管研究所他完成了一个研究奖学金。他是核酸酶和基因工程领域多项专利的合作发明者和50多个科学出版物的合作者,合作编辑一本题为Site-directed Insertion of Transgenes的书。自从2004年以来,作为ellectis研究部门的领导者,他帮助Cellectis技术的发展。自2012年以来Philippe Duchateau一直担任首席科学家。
Philippe Duchateau joined Cellectis in 2001 to pioneer the field of genome engineering and has served as Chief Scientific Officer since 2012. After receiving his Ph.D. in 1993 in biochemistry and molecular biology at the Institut Pasteur (Lille, France), he completed a research fellowship from 1993 to 2001 at the University of California, San Francisco (United States) within the Cardiovascular Research Institute. He is co inventor of numero patents in the field of nucleases and genome engineering and co author on more than 50 scientific publications and co editor of one book entitled "Site directed Insertion of Transgenes." As head of Cellectis's Research department since 2004, he helped to the development of the key Cellectis technologies.
Marie Bleuenn Terrier

Marie Bleuenn Terrier,她于2008年加入Cellectis公司,担任法律顾问,并于2013年被任命为总法律顾问。加入Cellectis公司之前,她曾担任Pfizer公司(2004年至2006年)、Boehringer公司(从2006年到2008年)的法律顾问。她曾一直担任我们的董事会秘书(2015年以来)。她持有the Panthéon La Sorbonne University(位于巴黎)的法律硕士学位。


Marie Bleuenn Terrier joined Cellectis as Legal Counsel in 2008, and was appointed General Counsel in 2013. Prior to joining Cellectis, she worked as Legal Counsel for Pfizer from 2004 to 2006, and for Boehringer Ingelheim from 2006 to 2008. Marie Bleuenn Terrier also serves as Secretary of board of directors since 2015. From July 2020 to September 2022, Mrs. Terrier served as president of Standing Ovation S.A.S. She holds a Master's degree in Law from the Panthéon La Sorbonne University in Paris.
Marie Bleuenn Terrier,她于2008年加入Cellectis公司,担任法律顾问,并于2013年被任命为总法律顾问。加入Cellectis公司之前,她曾担任Pfizer公司(2004年至2006年)、Boehringer公司(从2006年到2008年)的法律顾问。她曾一直担任我们的董事会秘书(2015年以来)。她持有the Panthéon La Sorbonne University(位于巴黎)的法律硕士学位。
Marie Bleuenn Terrier joined Cellectis as Legal Counsel in 2008, and was appointed General Counsel in 2013. Prior to joining Cellectis, she worked as Legal Counsel for Pfizer from 2004 to 2006, and for Boehringer Ingelheim from 2006 to 2008. Marie Bleuenn Terrier also serves as Secretary of board of directors since 2015. From July 2020 to September 2022, Mrs. Terrier served as president of Standing Ovation S.A.S. She holds a Master's degree in Law from the Panthéon La Sorbonne University in Paris.
Stephan Reynier

Stephan Reynier于2011年4月加入Cellectis。他从2011年4月到2014年担任Ectycell(Cellectis的前子公司)的项目主管,负责管理和协调内部和外部合作项目,随后担任首席监管和合规官。作为首席监管和合规官,Reynier先生负责通过与EMA和FDA等监管机构建立密切互动来确保UCART产品系列的快速和成功开发,同时确保遵守适用的法规,监管指南和质量保证标准。Reynier先生拥有丰富的经验,从他之前在Voisin Consulting Life Sciences担任高级总监和在Gilead Sciences担任欧洲副总监医疗事务,在药物和生物制剂开发的监管策略的设计和实施方面,专注于细胞和基因治疗。Reynier先生毕业于法国农业工程师,并在加拿大多伦多大学(University of Toronto,Canada)获得化学工程理学硕士学位。


Stephan Reynier joined Cellectis in April 2011. He serves as Chief Regulatory and Pharmaceutical Compliance Officer. Mr. Reynier has extensive experience, from his previo positions as Senior Director at Voisin Consulting Life Sciences and European Associate Director Medical Affairs at Gilead Sciences, in the design and implementation of regulatory strategies for the development of drugs and biologics, with a strong foc on cell and gene therapy. Mr Reynier graduated as Agro Engineer in France and received a Master of Science in Chemical Engineering from the University of Toronto, Canada.
Stephan Reynier于2011年4月加入Cellectis。他从2011年4月到2014年担任Ectycell(Cellectis的前子公司)的项目主管,负责管理和协调内部和外部合作项目,随后担任首席监管和合规官。作为首席监管和合规官,Reynier先生负责通过与EMA和FDA等监管机构建立密切互动来确保UCART产品系列的快速和成功开发,同时确保遵守适用的法规,监管指南和质量保证标准。Reynier先生拥有丰富的经验,从他之前在Voisin Consulting Life Sciences担任高级总监和在Gilead Sciences担任欧洲副总监医疗事务,在药物和生物制剂开发的监管策略的设计和实施方面,专注于细胞和基因治疗。Reynier先生毕业于法国农业工程师,并在加拿大多伦多大学(University of Toronto,Canada)获得化学工程理学硕士学位。
Stephan Reynier joined Cellectis in April 2011. He serves as Chief Regulatory and Pharmaceutical Compliance Officer. Mr. Reynier has extensive experience, from his previo positions as Senior Director at Voisin Consulting Life Sciences and European Associate Director Medical Affairs at Gilead Sciences, in the design and implementation of regulatory strategies for the development of drugs and biologics, with a strong foc on cell and gene therapy. Mr Reynier graduated as Agro Engineer in France and received a Master of Science in Chemical Engineering from the University of Toronto, Canada.
Arthur Stril

Arthur Stril于2018年7月加入Cellectis,担任Vice President,负责企业发展,并负责项目管理,战略和业务发展。Arthur的职业生涯始于the European Commission&8217;s Directorate for Competition,控制全球制药合并。后来,他成为法国卫生部医院融资部门的负责人。Stril先生毕业于the&201;Cole Normale Sup&233;Rieure,Paris&Cambridge University,并持有the Universit&233;Paris-Descartes免疫治疗文凭。Stril先生也是the French Corps des Mines的成员。


Arthur Stril joined Cellectis in 2018 as Vice President, Corporate Development. He was appointed Chief Biness Officer in 2020 and Chief Biness Officer and Interim Chief Financial Officer in 2024. He currently serves as Chief Financial Officer and Chief Biness Officer since January 2025. Mr. Stril serves on the board of directors of Primera Therapeutics, Inc. since 2023, serving as a director designated by Cellectis. Mr. Stril began his career at the European Commission's Directorate General for Competition, controlling global pharmaceutical mergers. He later became Head of the Hospital Financing Unit at the French Ministry of Health. Mr. Stril graduated from the cole Normale Supérieure, Paris and Cambridge University, and holds a diploma in Immunotherapy from the Université Paris Descartes. Mr. Stril is also a member of the French Corps des Mines and is a member of the advisory board of Life Science Cares, a not for profit organisation.
Arthur Stril于2018年7月加入Cellectis,担任Vice President,负责企业发展,并负责项目管理,战略和业务发展。Arthur的职业生涯始于the European Commission&8217;s Directorate for Competition,控制全球制药合并。后来,他成为法国卫生部医院融资部门的负责人。Stril先生毕业于the&201;Cole Normale Sup&233;Rieure,Paris&Cambridge University,并持有the Universit&233;Paris-Descartes免疫治疗文凭。Stril先生也是the French Corps des Mines的成员。
Arthur Stril joined Cellectis in 2018 as Vice President, Corporate Development. He was appointed Chief Biness Officer in 2020 and Chief Biness Officer and Interim Chief Financial Officer in 2024. He currently serves as Chief Financial Officer and Chief Biness Officer since January 2025. Mr. Stril serves on the board of directors of Primera Therapeutics, Inc. since 2023, serving as a director designated by Cellectis. Mr. Stril began his career at the European Commission's Directorate General for Competition, controlling global pharmaceutical mergers. He later became Head of the Hospital Financing Unit at the French Ministry of Health. Mr. Stril graduated from the cole Normale Supérieure, Paris and Cambridge University, and holds a diploma in Immunotherapy from the Université Paris Descartes. Mr. Stril is also a member of the French Corps des Mines and is a member of the advisory board of Life Science Cares, a not for profit organisation.
Steven Doares

Steven Doares于2020年7月加入Cellectis,担任美国制造高级副总裁和北卡罗来纳州罗利制造工厂场长。Doares博士负责在罗利部署Cellectis’;制造设施,为Cellectis’;目前的免疫肿瘤UCART候选产品提供临床和商业供应。加入Cellectis之前,2010年至2020年,Doares博士在Biogen,Inc.工作,最近担任全球制造科学副总裁,负责从临床到商业化阶段的流程的CGMP制造技术转移,包括Biogen’;S治疗产品组合的内部和外部。Doares博士拥有乔治亚大学生物化学博士学位。


Steven Doares joined Cellectis in July 2020 as Senior Vice President, Manufacturing and Site Head of the Raleigh, North Carolina manufacturing facility. Dr. Doares is responsible for the deployment of Cellectis' manufacturing facility in Raleigh, for clinical and commercial supplies of the Cellectis' current immuno oncology UCART product candidates. Prior joining Cellectis, Dr. Doares worked at Biogen, Inc. from 2010 to 2020, most recently serving as Vice President, Global Manufacturing Sciences, responsible for technology transfer into cGMP manufacturing of processes from clinical through commercialization stages for Biogen's therapeutic product portfolio, both internally and externally. Dr. Doares holds a Ph.D. in Biochemistry from the University of Georgia.
Steven Doares于2020年7月加入Cellectis,担任美国制造高级副总裁和北卡罗来纳州罗利制造工厂场长。Doares博士负责在罗利部署Cellectis’;制造设施,为Cellectis’;目前的免疫肿瘤UCART候选产品提供临床和商业供应。加入Cellectis之前,2010年至2020年,Doares博士在Biogen,Inc.工作,最近担任全球制造科学副总裁,负责从临床到商业化阶段的流程的CGMP制造技术转移,包括Biogen’;S治疗产品组合的内部和外部。Doares博士拥有乔治亚大学生物化学博士学位。
Steven Doares joined Cellectis in July 2020 as Senior Vice President, Manufacturing and Site Head of the Raleigh, North Carolina manufacturing facility. Dr. Doares is responsible for the deployment of Cellectis' manufacturing facility in Raleigh, for clinical and commercial supplies of the Cellectis' current immuno oncology UCART product candidates. Prior joining Cellectis, Dr. Doares worked at Biogen, Inc. from 2010 to 2020, most recently serving as Vice President, Global Manufacturing Sciences, responsible for technology transfer into cGMP manufacturing of processes from clinical through commercialization stages for Biogen's therapeutic product portfolio, both internally and externally. Dr. Doares holds a Ph.D. in Biochemistry from the University of Georgia.
Kyung Nam Wortman

Kyung Nam Wortman于2020年11月加入Cellectis,担任执行副总裁兼首席人力资源官,负责确保公司通过招聘和留住顶尖人才来推进其路线图。她还致力于进一步发展和提升Cellectis’;充满活力和包容性的文化,同时优化公司的人力资源职能。加入Cellectis之前,Nam-Wortman女士自2014年10月起担任Achillion的高级副总裁、人力资源主管、信息技术、设施和内部沟通主管,该公司最近于2020年1月被Alexion收购。在Achillion任职之前,Nam-Wortman女士是Zoetis的副总裁兼全球人才和组织能力主管,她支持辉瑞公司的动物健康业务部门通过首次公开募股(IPO)分拆上市,并负责Zoetis公司的全球人才管理职能,以支持该公司在全球的发展。她还担任Pfizer’;的业务单元、部门和职能部门的各种人力资源领导职务,负责区域和全球事务。除了在生物技术/生物制药领域的经验,Nam-Wortman女士在咨询行业拥有14年的经验,专注于Delta Consulting Group和IBM的战略和组织变革管理。她在纽约大学斯特恩商学院(New York University Stern School of Business)获得营销学士学位,在新的社会研究学院(New School of Social Research)获得人力资源管理/组织发展硕士学位。


Kyung Nam Wortman joined Cellectis in November 2020 as Executive Vice President, Chief Human Resces Officer. Before joining Cellectis, Ms. Nam Wortman was Senior Vice President, Head of Human Resces, Head of Information Technology, Facilities and Internal Communications at Achillion (acquired by Alexion in January 2020) since October 2014. Prior to her tenure at Achillion, Ms. Nam Wortman was Vice President and Head of Global Talent and Organization Capability at Zoetis, where she supported the spin off of Pfizer's animal health biness unit through its IPO and was responsible for the stand up of Zoetis' global talent management function to support the company's growth worldwide. She also held vario human resce leadership roles for Pfizer's biness units, divisions, and functions with regional and global accountabilities. In addition to her experience in biotech/biopharma, Ms. Nam Wortman has significant experience in the consulting indtry foced on strategic and organization change management from Delta Consulting Group and IBM. She received her bachelor's degree in marketing from New York University Stern School of Biness and MS in human resces management and organization development from the New School of Social Research.
Kyung Nam Wortman于2020年11月加入Cellectis,担任执行副总裁兼首席人力资源官,负责确保公司通过招聘和留住顶尖人才来推进其路线图。她还致力于进一步发展和提升Cellectis’;充满活力和包容性的文化,同时优化公司的人力资源职能。加入Cellectis之前,Nam-Wortman女士自2014年10月起担任Achillion的高级副总裁、人力资源主管、信息技术、设施和内部沟通主管,该公司最近于2020年1月被Alexion收购。在Achillion任职之前,Nam-Wortman女士是Zoetis的副总裁兼全球人才和组织能力主管,她支持辉瑞公司的动物健康业务部门通过首次公开募股(IPO)分拆上市,并负责Zoetis公司的全球人才管理职能,以支持该公司在全球的发展。她还担任Pfizer’;的业务单元、部门和职能部门的各种人力资源领导职务,负责区域和全球事务。除了在生物技术/生物制药领域的经验,Nam-Wortman女士在咨询行业拥有14年的经验,专注于Delta Consulting Group和IBM的战略和组织变革管理。她在纽约大学斯特恩商学院(New York University Stern School of Business)获得营销学士学位,在新的社会研究学院(New School of Social Research)获得人力资源管理/组织发展硕士学位。
Kyung Nam Wortman joined Cellectis in November 2020 as Executive Vice President, Chief Human Resces Officer. Before joining Cellectis, Ms. Nam Wortman was Senior Vice President, Head of Human Resces, Head of Information Technology, Facilities and Internal Communications at Achillion (acquired by Alexion in January 2020) since October 2014. Prior to her tenure at Achillion, Ms. Nam Wortman was Vice President and Head of Global Talent and Organization Capability at Zoetis, where she supported the spin off of Pfizer's animal health biness unit through its IPO and was responsible for the stand up of Zoetis' global talent management function to support the company's growth worldwide. She also held vario human resce leadership roles for Pfizer's biness units, divisions, and functions with regional and global accountabilities. In addition to her experience in biotech/biopharma, Ms. Nam Wortman has significant experience in the consulting indtry foced on strategic and organization change management from Delta Consulting Group and IBM. She received her bachelor's degree in marketing from New York University Stern School of Biness and MS in human resces management and organization development from the New School of Social Research.
Adrian Kilcoyne

Adrian Kilcoyne,自2022年10月起担任Celularity Inc.执行副总裁兼首席医疗官。在加入Celularity Inc.公司之前,他于2021年4月至2022年9月担任Humanigen的首席医疗官,负责构建其肿瘤学和免疫学产品组合,重点关注细胞因子途径、CAR-T治疗相关毒性以及实体瘤中的抗体药物偶联物。从2019年6月到2021年4月,Kilcoyne博士在阿斯利康担任执行团队不可或缺的成员,从2020年5月开始担任全球肿瘤学证据生成和外部联盟副总裁,并从2019年6月开始担任副总裁、美国医疗事务主管和肿瘤学HEOR。在阿斯利康任职期间,他负责制定、开发和交付完全集成的全球证据战略。从2013年11月到2019年6月,Kilcoyne博士在Celgene担任过各种职务。Kilcoyne博士拥有都柏林三一学院的医学博士学位、伦敦大学的医学硕士学位和华威商学院的工商管理硕士学位。除了在同行评审期刊上发表多篇文章外,他还与人合著了《牛津医药医学专家手册》。


Adrian Kilcoyne,has served as Celularity Inc. Executive Vice President and Chief Medical Officer since October 2022. Prior to joining Celularity Inc. company, he served as the Chief Medical Officer of Humanigen from April 2021 to September 2022, where he was responsible for building its oncology and immunology portfolio focused on the cytokine pathway, CAR-T therapy related toxicity, and antibody drug conjugates in solid tumors. From June 2019 to April 2021 Dr. Kilcoyne served as an integral member of the executive team at AstraZeneca as the Vice President of Global Oncology Evidence Generation and External Alliances beginning May 2020, and from June 2019 until then as Vice President, Head of U.S. Medical Affairs and HEOR, Oncology. During his time at AstraZeneca, he was responsible for the creation, development, and delivery of the fully integrated global evidence strategy. From November 2013 to June 2019, Dr. Kilcoyne held various roles at Celgene. Dr. Kilcoyne holds an M.D. from Trinity College in Dublin, an M.P.H. from the University of London, and an M.B.A. from Warwick Business School. Along with multiple publications in peer review journals, he co-authored the Oxford Specialist Handbook of Pharmaceutical Medicine.
Adrian Kilcoyne,自2022年10月起担任Celularity Inc.执行副总裁兼首席医疗官。在加入Celularity Inc.公司之前,他于2021年4月至2022年9月担任Humanigen的首席医疗官,负责构建其肿瘤学和免疫学产品组合,重点关注细胞因子途径、CAR-T治疗相关毒性以及实体瘤中的抗体药物偶联物。从2019年6月到2021年4月,Kilcoyne博士在阿斯利康担任执行团队不可或缺的成员,从2020年5月开始担任全球肿瘤学证据生成和外部联盟副总裁,并从2019年6月开始担任副总裁、美国医疗事务主管和肿瘤学HEOR。在阿斯利康任职期间,他负责制定、开发和交付完全集成的全球证据战略。从2013年11月到2019年6月,Kilcoyne博士在Celgene担任过各种职务。Kilcoyne博士拥有都柏林三一学院的医学博士学位、伦敦大学的医学硕士学位和华威商学院的工商管理硕士学位。除了在同行评审期刊上发表多篇文章外,他还与人合著了《牛津医药医学专家手册》。
Adrian Kilcoyne,has served as Celularity Inc. Executive Vice President and Chief Medical Officer since October 2022. Prior to joining Celularity Inc. company, he served as the Chief Medical Officer of Humanigen from April 2021 to September 2022, where he was responsible for building its oncology and immunology portfolio focused on the cytokine pathway, CAR-T therapy related toxicity, and antibody drug conjugates in solid tumors. From June 2019 to April 2021 Dr. Kilcoyne served as an integral member of the executive team at AstraZeneca as the Vice President of Global Oncology Evidence Generation and External Alliances beginning May 2020, and from June 2019 until then as Vice President, Head of U.S. Medical Affairs and HEOR, Oncology. During his time at AstraZeneca, he was responsible for the creation, development, and delivery of the fully integrated global evidence strategy. From November 2013 to June 2019, Dr. Kilcoyne held various roles at Celgene. Dr. Kilcoyne holds an M.D. from Trinity College in Dublin, an M.P.H. from the University of London, and an M.B.A. from Warwick Business School. Along with multiple publications in peer review journals, he co-authored the Oxford Specialist Handbook of Pharmaceutical Medicine.