... are currently seeking full-time, Regulatory Submissions Technical Advisors to join ... at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory advice to support clinical trial ...
... Biotechnology2+ years of experience in regulatory affairs within the pharmaceutical industryGeneral understanding of the pharmaceutical industry and regulatory environment in drug development and ...
... years of relevant experience in regulatory affairs and pharmaceutical industry Understanding of the pharmaceutical industry, and regulatory processes related to license maintenance ...
... audits to assess compliance with regulatory standards. Identify areas of non- ... 4 years of experience in regulatory compliance in the international environment. ... to interpret and apply complex regulatory requirements to business operations. Excellent ...
... and changing local and European regulatory legislation Managing a team of Regulatory Affairs ( x2) Participating in bid defense ...
... we are looking for a Regulatory Affairs Quality Analyst 3 to join ...
... systemsOur requirements Relevant experience in regulatory affairs, pharmaceutical industry (familiarity with post-approval CMC regulatory procedures and ICH CTD documentation) ...
... Specific Requirements (MSRs) across Global Regulatory Affairs (GRA) across the lifecycle in support of regulatory submissions for Pharma and Vaccines ... 5 + Relevant experience (in regulatory affairs, pharmaceutical industry, life sciences research, ...
... . Support cross CEE BU Corporate Affairs initiatives, incl. executive board members ... closely with CEE CA Corporate Affairs Manager, HR Team members, as ... either end-to-end Corporate Affairs professional or acting as external ...
... a key member of the Regulatory & Medical Affairs department, you will provide strategic direction and leadership across a broad range of medical affairs activities, ensuring the highest quality ...