Regulatory Submissions Jobs in Beijing

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAtThermoFisher Scientificyoulldiscover 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 healthiercleane...

Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products in Kazakhstan while taking a step further in your professional career.Office-based in AlmatyYou will:Prepare clinical trial sub...

Accounting Manager ChinaLocation: BeijingIf youre ready to have an impact in a career that makes a difference Mölnlycke could be your next step. Youll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And youll be developing yourself in a glo...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 co...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Regulatory Affairs Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acro...

Job SummaryCollaborate with departmental and cross-functional colleagues (eg. G-CMC WSR WRO and PGS) to leverage and share both technical & regulatory knowledge align expectations and manage planning and monitoring activities to mitigate risks contribute to global regulatory strategies deliver exped...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

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At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Principal Medical Writing - Make an Impact at the Forefront of InnovationAs a Principal Medical Writer you will serve as the primary author by writing and providing input on routine documents such as clinical st...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummary of Essential Functions:Prepares reviews and coordinates local regulatory submissions (MoH EC additional special national local applications if applicable e.g. gene therapy approvals viral safety dossiers import licen...

Coordinate prepare or review regulatory submissions for domestic or international projects.ResponsibilitiesList up to 10 main responsibilities for the job. Include information about the accountability and scope.Provide technical review of data or reports that will be incorporated into regulatory sub...