... tool Monitoring and reporting of regulatory change status against an agreed ... assigns a priority based on regulatory authority and publication type Determines ... the disputes with consideration from Regulatory Change Team (‘’RCT’’) Our Ideal ...
... responsible Manager. Within the EMEA Regulatory Affairs organization, the main objectives of ... . Key Responsibilities: As a Senior Regulatory Affairs Specialist, you will partner with ... in the area of quality, regulatory affairs or R&D. You have ...
... .Join us The Senior Director, Regulatory Affairs is a leader, who provides ... the drug development process and regulatory submission and approval process required. • Experience working in a regulatory affairs leadership role with sole responsibility ...
... responsible Manager. Within the EMEA Regulatory Affairs organization, the main objectives of ... . You will also support the Regulatory Affairs team and other functions with ... in the area of quality, regulatory affairs or R&D. You have ...
... to the VP, Global Regulatory Affairs, the Manager, Regulatory Affairs will key part in guiding and executing regulatory strategies to advance our innovative ... 7 years of experience in regulatory affairs within pharmaceutical or biotechnology industry. ...
... to the VP, Global Regulatory Affairs, the Manager, Regulatory Affairs will key part in guiding and executing regulatory strategies to advance our innovative ... 7 years of experience in regulatory affairs within pharmaceutical or biotechnology industry. ...
... .Join us The Senior Director, Regulatory Affairs is a leader, who provides ... the drug development process and regulatory submission and approval process required. •Experience working in a regulatory affairs leadership role with sole responsibility ...
... (RAPD) The Regulatory Affairs Project Director (RAPD) is an experienced regulatory specialist with strong project management capabilities who takes on critical leadership roles for particularly complex and high priority global regulatory projects and ...
... 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 ...
... 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 ...