Weiss Yang

Assitant Vice President, Oncology Clinical Development @ Simcere Zaiming

About

- Good knowledge in Oncology - 3 years’ experience in hospital, and 10+ years ‘experience in multi-national and local pharmaceutical companies - Experience in clinical development in solid tumors and hematology from Phase I to Phase IV - Experience in leading a team and people development - Experience in project management and cross-functions & cross-culture communication

Country

China

City

Pudong

Industry

Pharmaceuticals

Skill

Oncology Clinical Research, Investigational New Drug Application (IND), Business Development, Oncology, Clinical Trials, Medical Affairs, Biotechnology, Pharmaceutical Industry, Clinical Development, Medicine, Clinical Research, Lifesciences, Pharmacovigilance, GCP, Drug Development, CTMS, Medical Writing, Therapeutic Areas, Hematology, Hospitals

Experience

assitant vice president

Simcere Zaiming

2023-11 - Present · 2 yrs 11 mos

Shanghai, China

be the team lead of clinical science team. be responsible for the clinical development of all oncology pipeline. support the license in/out assets.

Executive Director

Simcere Pharmaceutical Group

2022-5 - 2023-10 · 1 yr 6 mos

Shanghai, China

header of medical science team

Senior Director

Simcere Pharmaceutical Group

2020-4 - 2022-5 · 2 yrs 2 mos

Medical Director, Head of Early Phase Clinical Development

HUTCHMED

2017-7 - 2020-3 · 2 yrs 9 mos

Shanghai Suburb, China

• Accountable for early clinical phase projects (solid tumor/AML/lymphoma) • Accountable for IND filing (US & China), investigator’s brochure, protocol, medical monitoring, investigator’s meeting and project management (China & Australia) • Team leader of early phase clinical development (4-5 direct subordinates)

Associate Medical Director

HUTCHMED

2015-5 - 2017-7 · 2 yrs 3 mos

Shanghai Suburb, China

• As Clinical project leader, leading project teams to support clinical development in solid tumor and lymphoma • Accountable for clinical protocol, medical monitoring and project management of studies (China and Australia)

Clinical Scientist

Roche

2014-10 - 2015-4 · 7 mos

Shanghai City, China

• Support CDP (clinical development plan) development in China • Lead clinical study protocol/ICF development (phase III & PK) • Support CTA filing

Medical Manager

Roche

2012-5 - 2015-4 · 3 yrs

• Lead product medical strategy development; support disease area strategy and product marketing strategy development; support new indication (gastric cancer) launch in China • Design/exctute phase IV registry study and support Investigator initiated studies (IIS) • Organise large scale(1000+ KOLs) medical eduction activities for data communication; organise the Advisor Board meeting for consulting • Co-lead the KOL profiling and national KOL communication

Medical Advisor

Pfizer

2011-11 - 2012-4 · 6 mos

Shanghai City, China

• Provide medical support for 3 oncology products in gastrointestinal cancer /lung cancer/AML in China • Support the product marketing strategy • Support investigator initiate study in China • Preparation for new indication (GEP-NET) launch

Regional Medical Advisor

Pfizer

2010-8 - 2011-11 · 1 yr 4 mos

Shanghai City, China

• Provide medical support for 5 oncology products in 6 therapeutic areas in local • Collect, analyze and report local customer medical insights to assist business decision making • Prepare new product launch • Provide internal training for commercial team

Resident Physician

Shanghai No.6 People's Hospital Affiliated to Shanghai Jiaotong University

2007-8 - 2010-7 · 3 yrs

Shanghai City, China

• Resident under supervision of director • Design IIS and take part in industry sponsored studies (ChiCTR-TRC-09000569) • Design and conduct in vitro and in vivo animal studies