超尘 王

超尘

Sr. Director of Program Management Office @ AnHeart Therapeutics

Country

-

City

China

Industry

Pharmaceuticals

Skill

临床试验, 制药业, 临床开发, 良好药品临床试验规范, 临床试验管理系统, 标准作业程序, 药品开发, ICH-GCP

Experience

AnHeart Therapeutics

Sr. Director of Program Management Office

AnHeart Therapeutics

LinkedIn
2021-9 - Present · 5 yrs

Boston, Massachusetts, United States

Everest Medicines

Director Program Management Office

Everest Medicines

LinkedIn
2020-9 - 2021-9 · 1 yr 1 mo

Beijing, China

IQVIA

Director of Clinical Operation

IQVIA

LinkedIn
2019-3 - 2020-9 · 1 yr 7 mos

Beijing,China

Responsible for managing of the CRA Resource manager in Beijing Core Team 1. Directly managing 9 CRAs Line managers and coach for high performance team 2. Indirectly managing over 70 CRAs to achiever annual revenue 3. Support study team to achiever study’s milestone timely with high quality 4. Ensure resource balance

IQVIA

Associate Director of Clinical Operation

IQVIA

LinkedIn
2017-4 - 2019-3 · 2 yrs

北京

Responsible for managing of the CRA Resource manager in Beijing Core Team 1. Directly managing 9 CRAs Line managers and coach for high performance team 2. Indirectly managing over 70 CRAs to achiever annual revenue 3. Support study team to achiever study’s milestone timely with high quality 4. Ensure resource balance

AstraZeneca

Senior Project Manager

AstraZeneca

LinkedIn
2013-2 - 2017-4 · 4 yrs 3 mos

Beijing

Experienced in more than 10 studies from Phase III and Phase IV, Post-market study Therapeutic experience includes Cardiovascular diseases, Diabetes, Rheumatoid Arthritis, Respiratory, Infection, Solid Tumour Canner and Immune Oncology  1. Accountable for the deliverables of the responsible studies according to KPIs  2. Conduct quality control activities to ensure study quality  3. Prepare budget plan and control budget according to KPIs  4. Communicate with all stakeholders including global/local study team, national investigator, other functions to share study status, escalate issues and get necessary supports  5. Organize investigator meetings  6. Manage the third party vendors, such as SMO and central l lab

Novartis

Clinical Study Manager

Novartis

LinkedIn
2012-6 - 2013-2 · 9 mos

Beijing, China

Working in ICRO China and responsible for the operation of phase II and phase III studies Jun 2012—Feb 2013, Clinical study manager Jul, 2010-May 2012Jul, SCRA/Lead CRA Apr 2008-Jun 2010, CRA, in pre-marketing study

Novartis

CRA&Sr. CRA

Novartis

LinkedIn
2008-4 - 2012-6 · 4 yrs 3 mos

Beijing

Working in ICRO China and responsible for the operation of phase II and phase III studies Jun 2012—Feb 2013, Clinical study manager

百诺科医学咨询公司

Clinical Research Assistant

百诺科医学咨询公司

2007-7 - 2008-4 · 10 mos

China, Beijing

翰博瑞强医学科技服务公司

Clinical Research Assistant

翰博瑞强医学科技服务公司

2006-6 - 2007-6 · 1 yr 1 mo

China, Beijing

Education

Dalian University of Foreign Languages

Dalian University of Foreign Languages

LinkedIn

英语

2004 - 2006 · 2 yrs
Chengdu University of Traditional Chinese Medicine

Chengdu University of Traditional Chinese Medicine

LinkedIn

临床医学

超尘 's Contact Information

Email

******@***.com

Phone

(**) *** ****

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