Title: Manager, Global Regulatory Affairs Company: Ipsen Innovation (SAS) Job Description: Purpose of the... of professional experience in the pharmaceutical industry, including in Global Drug Development Regulatory Affairs. Good written...
, Global Regulatory Affairs (GRA) Manager’s Job Title: VP, Global Regulatory Affairs, Oncology Ipsen Job Profile...Title: Director, Global Regulatory Affairs, Oncology Precision Medicine Company: Ipsen Innovation (SAS...
for humanity. Learn more at governmental affairs manager Location: Franc e, Issy Les Moulineaux Contract: full-time..., permanent The governmental affairs manager within the External Affairs team is tasked with building an institutional...
Manager, CMC Regulatory Strategy Division / Function: Global Regulatory Affairs (GRA) Prepare throughout the different... with Global Regulatory Affairs Therapeutic Area leads to integrate the CMC regulatory strategy to the overall regulatory strategy...
expected and actual timelines for submissions, approvals from Local Regulatory Affairs (LRA) monitor new launches...: Minimum 10 years’ experience in CMC regulatory affairs field in a management role Ideal: Significant depth of change management...
) Job Description: Job Title: Sr Director CMC Regulatory Strategy – Small molecules Division / Function: Global Regulatory Affairs (GRA... regulatory community and particularly with Ipsen Global Regulatory Affairs Therapeutic Area leads to integrate the CMC regulatory...
Medical Aairs, Global Regulatory Affairs, Clinical, Biostatistics, Public Affairs, Marketing etc. Stay abreast of the... and credible collaborations with partners in Medical Affairs, Clinical, Market Access, Regulatory and other groups, as well...
pharmaceutical industry worldwide. Your mission We are recruiting a System QA Manager, under the direct supervision of the.... Department product coverage: The functions within the scope work on all the Group's products, whatever their regulatory status...
-monitoring the assigned international Phase I to III clinical studies in accordance with regulatory requirements, Good Clinical..., such as regulatory and ethics committee documents for submission, oversee site Clinical Trial Agreements preparation and control...