Regulatory Submissions Jobs in Beijing

The Program Managers responsibilities include providing comprehensive support for regulatory and quality activities in China and the APAC region. This includes product submissions market initiatives and policy interactions.- Oversee regulatory submissions launch readiness design changes and medical...

Job Descriptionresponsible for study initation and clinical study conductionresponsible for clinical development plan execution and owner of clinical studies in dedicated disease areaThis individual will serve as the key interface between headquarter project development team and China R&D center. Th...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

Career CategoryRegulatoryJob DescriptionJob Summary: n Develop China registration strategy and implement regulatory submissions (China IND/CTN etc.) for products within Amgens portfolio in compliance with corporate standards and local regulatory requirements. n Develop HA communication strategy for...

Career CategoryRegulatoryJob DescriptionJob Summary: n Develop China registration strategy and implement regulatory submissions (e.g. China IND/ CTN etc.) for products within Amgens portfolio in compliance with corporate standards and local regulatory requirements. n Develop HA communication strateg...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner an...

Job DescriptionRole & ResponsibilityThis position serves as the role of clinical research physician who will be in charge of the Ph1 study in Chinese participants with hematological malignancies. The responsibility of this role is to provide strong capability to lead for study determination and prel...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeResponsibilities may include the following an...

JOB DESCRIPTION:EXPERIENCE:Over 5 years working experience in regulatory affairs or R&D for pharmaceuticals including more than 3 years in regulatory affairs.Solid registration project management skills;Effective problem solving and planning capabilities;Good knowledge of NMPA/CDE regulations and...

Job DescriptionResponsibilities:Work closely with Global colleagues to prepare dossiers and documents for product registration in China. Provide guidance and regulations required by the Chinese authorities for the documentation preparations. Independently undertake theproject.Work closely with inter...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

Job DescriptionResponsibilities:Work closely with Global colleagues to prepare dossiers and documents for product registration in China. Provide guidance and regulations required by the Chinese authorities for the documentation preparations. Independently undertake theproject.Work closely with inter...