Found Related Results: 20

Director, Key External Expert (KEE) Liaison

Director, Key External Expert (KEE) Liaison Job Title: Director, Key External Expert (KEE) Liaison Location: Florham Park, NJ Primary Function The Director, Key External Expert (KEE) Liaison will be part of the HUTCHMED US Commercial org

Commercialization, USA | 2021-09-13

Sr. Brand Director, Colorectal Cancer

Job Title: Sr. Brand Director, Colorectal Cancer Location: Florham Park, NJ Primary Function As an integral member of the US Marketing Team and the International Product Team, the Sr. Brand Director, Colorectal Cancer, will lead the pre

Commercialization, USA | 2021-09-13

Director, New Products Marketing

Job Title: Director, New Products Marketing Location: Florham Park, NJ Primary Function The Director of New Products is an integral member of both the US Marketing Team and the cross-functional International Product Development Tea

Clinical Operations and Regulatory Affairs, Commercialization, Research and Development, USA | 2021-09-01

Associate Director/Director, Pharmaceutical Program Management

Associate Director/Director, Pharmaceutical Program Management Primary Functions This role will be responsible for ensuring that timelines, milestones, deliverables and budgets are met and executed with excellence. Partnering with multi-functional

Commercialization, USA | 2021-09-01

Oncology Account Manager (Launch Excellence Team)

Job Title: Oncology Account Manager- Launch Excellence Team - Job Category: Exempt/Non-Exempt Department/Group: Commercial/Sales Travel Required: 50% Location: Remote Base-City Locations Position Type: Field Sales Primary Function

Commercialization, USA | 2021-09-01

Director, Digital Marketing

Job Title: Director, Digital Marketing Job Category: Exempt/Non-Exempt Department/Group: Marketing Travel Required: Location: Florham Park, NJ Position Type: Primary Functions This position is a highly valued member of the Ma

Commercialization, USA | 2021-09-01

Director, US Field Market Access (Remote, WEST)

Job Title: Director, US Field Market Access Job Category: Exempt/Non-Exempt Department/Group: US Market Access Travel Required: up to 50% Location: Remote, WEST Position Type: Market Access Primary Functions The Director of US Fiel

Clinical Operations and Regulatory Affairs, Hong Kong | 2021-08-09

Senior Manager, Medical Safety/ Pharmacovigilance

Job Title: Senior Manager, Medical Safety /Pharmacovigilance Directly report to: Director, Medical Affairs Primary Responsibilities Provide medical and safety expertise as the Medical Safety and Pharmacovigilance representative i

Commercialization, Hong Kong | 2021-07-22

Director, Medical Affairs

Key Responsibilities: Be the scientific expert on the assigned therapy area, disease area, clinical practice and competitor landscape; Handling pre-launching, providing professional medical advice in clinical aspect, and medical affairs activiti

Commercialization, USA | 2021-06-22

Principal Medical Science Liaison – Location Flexible

Primary Function:The Principal Medical Science Liaison (P-MSL) is responsible for providing fair balanced, objective, scientific information to health care professionals (HCPs), payers, advocacy groups and internal partners. The P-MSL provides s

General and Administration, USA | 2021-06-22

Paralegal/Contracts Manager

Job Title: Paralegal/Contracts Manager Job Category: Exempt/Non-Exempt Department/Group: Legal Travel Required: Location: Florham Park, NJ Position Type: Contract to Hire Level/Salary Range: Hiring Manager S

Manufacturing, USA | 2021-06-22

Associate Director/Director, GDP Quality Operations

Job Title: Associate Director/Director, GDP Quality Operations Job Category: Exempt/Non-Exempt Department/Group: Quality Assurance Travel Required: Yes, 25% Location: Florham Park, NJ Position Type:

Clinical Operations and Regulatory Affairs, USA | 2021-03-31

Director/Senior Director, Medical Safety Officer, Product Safety & Pharmacovigilance

Job Title: Director/Senior Director, Medical Safety Officer, Product Safety & Pharmacovigilance Directly report to: Vice President, Product Safety & Pharmacovigilance Department: Hutchison MediPharma International Primary

Clinical Operations and Regulatory Affairs, USA | 2021-02-24

Associate Director-Director, Biostatistics

Job Title: Associate Director-Director, Biostatistics Job Category: Exempt/Non-Exempt Department/Group: Biometrics Travel Required: NA Location: Florham Park, NJ Position Type: Full Time Level/Salary Range: Mid-Level Hiring Manager: Sr. D

Research and Development, Shanghai | 2020-05-21

Associate Scientist/ Scientist, Process R&D

Responsibilities Prepare process R&D related documents and reports to support IND and NDA. Update technical documents and effectively communicate with process R&D team. Support process R&D team to provide documentation for IND, NDA, I

Clinical Operations and Regulatory Affairs, Shanghai | 2020-05-11

Medical Marketing Manager

Responsibilities Provide medical input to marketing product team in product positioning and develop publication plan and clinical research proposal for the defined therapeutic areas Provide medical inputs in developing training program on disease

Clinical Operations and Regulatory Affairs, Shanghai | 2020-05-11

Clinical Project Manager

Primary Duties Management of clinical research project. Vendor (CRO, Lab, drug storage, etc.) supervision and management. Liaison with KOLs. Support IND and NDA filing. Quality control of the clinical research projects, such as co-monitoring.

Clinical Operations and Regulatory Affairs, Shanghai | 2020-05-11

Statistical Programmer

Primary Function The Statistical programmer/Senior Statistical Programmer is responsible for all statistical programming aspects at project level. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-developmen

Research and Development, Shanghai | 2020-05-11

Toxicologist, Director

Responsibilities: High profile discovery-and-development toxicology leadership role for design, implementation, interpretation and reporting safety profiles for small molecule therapeutics, including IND- and Phase III-enabling toxicology studies

Beijing, Clinical Operations and Regulatory Affairs | 2020-05-11

Senior Manager, Regulatory Affairs

Responsibilities Review product registration dossier and relevant documents Obtain IND & NDA approval as well as product registration license renewal as planed Coordinate with each function within HMPL from registration pathway Establish and