Our client, an exciting and growing Biotech Company, is seeking a Regulatory Affairs professional at the Senior Director level. Launch the company's regulatory strategy having leadership over all regulatory activities. This role will lead the North America regulatory strategy and work extremely clos...
The Director, Regulatory Affairs should have an advanced degree, preferably in the sciences, and have demonstrated application of regulatory expertise by at least 8+ years pharmaceutical industry experience. The Director, Regulatory Affairs is required to have excellent written and oral communicatio...
Associate Director/Director, Regulatory Affairs (Oncology). They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP of Regulatory Affairs and will be serving as the Lead for a US Phase III Oncology program. Serve as SM...
Executive Director Regulatory Affairs - Companion Diagnostics amp Precision Medicine. Significant experience in regulatory affairs and diagnostic related development (e. Experience with communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leaders...
Keeps current with latest Health Authority guidelines and provides Regulatory advice to members within Regulatory, and various associated departments within the Company. More Years of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs. Responsible for leadin...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
Director, Regulatory Affairs page is loaded. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submiss...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
Executive Director - Regulatory Affairs Team Leader - Precision Medicine. Application for : Executive Director - Regulatory Affairs Team Leader - Precision Medicine. Significant experience in regulatory affairs and diagnostic related development (e. Experience with communicating the regulatory strat...
The Senior Director, Regulatory Affairs - Clinical (Early Development), may be called upon to guide a team of Clinical Regulatory Affairs professionals providing strategic regulatory guidance to cross-functional project teams and responsible for product development and post marketing commitments. Th...
May represent the regulatory affairs function on Global Project Teams and be responsible for developing and implementing regulatory strategy (US and/or global) to achieve regulatory approvals and competitive product labels. Develop and direct implementation of global regulatory strategy for assigned...
Director, US Regulatory Affairs Strategy page is loaded. Director, US Regulatory Affairs Strategy. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that ...
Support the Regulatory Affairs Therapeutic Area Head for IN&F in this strategic leadership position responsible for leading and developing the global regulatory strategies, overseeing health authority interactions and for providing oversight for the preparation, review and evaluation of submission d...
Regulatory Affairs (2) Regulatory Affairs (4). Responsible for day-to-day Quality and Regulatory Operations for the company including the development and maintenance of a Quality Management System (QMS) supporting business operations and assuring compliance with existing and new...
The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review process and leadi...
Reporting to the Vice President of Global Regulatory Affairs (GRA), the Director of Chemical and Biological Regulatory Affairs will be responsible for setting the strategy for and leading the Chemical/Biological Regulatory Affairs team within the Global Regulatory Affairs organization. Assists in th...
As the Associate Director, Regulatory Affairs you will be responsible for leading the development and execution of US regulatory strategy for projects within an assigned Therapeutic Area (“TA”). Lead the development and execution of US regulatory strategy in conjunction with Global Regulatory Lead (...
Lead regulatory affairs activities, including the preparation of regulatory submissions and interactions with regulatory authorities. New Quality Assurance Regulatory Affairs Opportunity!. We are seeking Quality Assurance & Regulatory Affairs Manager to join our dynamic team. The successful candidat...
Lead regulatory affairs activities, including the preparation of regulatory submissions and interactions with regulatory authorities. We are seeking Quality Assurance & Regulatory Affairs Manager to join our dynamic team. The successful candidate will be responsible for overseeing all aspects of qua...
The Associate Director/Director plays a key role in developing and executing regulatory strategies and ensuring compliance with regulatory requirements that govern the development, registration and commercialization of livestock and poultry products (primarily medicated feed additives and water-solu...