... initial annual sales target for regulatory-specific work (outside of clinical ... therapies. Expertise in preparing complex regulatory documents including INDs, milestone briefing ... in its interpretation for global regulatory positions and strategy. Ability to ...
... . We are looking for a Regulatory Affairs Specialist Manager who will ... per week from home. This regulatory position has European responsibilities on ... . Collaborate in regional and global regulatory projects and act as a ...
... and in collaboration with the Regulatory Operations.Ensure regulatory compliance and maintenance of all ... Collaborate in regional and global regulatory projects and act as a ... of the network of regulatory consultants, including coordination with procurement ...
... teams on European regulatory requirements and changes in the regulatory landscape. Leads process improvement initiatives ... of experience in Regulatory Experience in the preparation submission of regulatory documentation to support clinical trials ...
... to market maturity). The Global Regulatory Centre in Poland is creating ... in Global Supply Chain, Global Regulatory Groups and GSK Local Operating ... industry, drug development environment, and regulatory processes Attention to detail with ...
... the wider business. OUR IMPACT Regulatory QA Reporting Intelligence Our team ... a team setting standards for regulatory reporting requirements implementation within the ...
... responsible Manager. Within the EMEA Regulatory Affairs organization, the main objectives ... successful business goals by supporting regulatory activities linked to pre- and ... in the area of quality, regulatory affairs or R&D. You ...
... 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 ...
... 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 ...
... .11. Provide day-to-day regulatory support, training, and assistance during ... .2. 3–5 years of Regulatory Affairs experience in an international ... detail.6. Ability to assess regulatory impact and formulate actionable strategies. ...