As a Senior Director of Regulatory Affairs, you will manage a team of regulatory professionals who analyze new regulatory requirements, work closely with the business to understand the impact and obli...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

Under direction of the Chief Quality Officer of the facility, the Director of Regulatory Affairs oversees the daily operations of the Regulatory Affairs Department across the health care setting and e...

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...

This role resides in the Global Development area of Regulatory Affairs, Global Patient Safety and Development Quality (RA, GPS and DQ) and the Director of Strategy Planning and Operations role will wo...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

This role resides in the Global Development area of Regulatory Affairs, Global Patient Safety and Development Quality (RA, GPS and DQ) and the Director of Strategy Planning and Operations role will wo...

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...

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 regulator...

Under direction of the Chief Quality Officer of the facility, the Director of Regulatory Affairs oversees the daily operations of the Regulatory Affairs Department across the health care setting and e...

Associate Director, CMC Regulatory Affairs. MannKind Corporation has an opening for an Associate Director, CMC Regulatory Affairs in Danbury, CT. Degree in Regulatory Affairs, Life Sciences, or a rela...

We are seeking an experienced and highly motivated Associate Director, Regulatory Affairs to support our expanding portfolio in the oncology area. Minimum of 5 years of regulatory affairs experience i...

The Executive Director, Global Regulatory Affairs Therapeutic Area Leader- GTAL provides strategic oversight and direction for regulatory activities on a global and/or regional scale across one or mor...

MannKind Corporation has an opening for an Associate Director, CMC Regulatory Affairs in Danbury, CT. Associate Director, CMC Regulatory Affairs. Degree in Regulatory Affairs, Life Sciences, or a rela...

The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide...

The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide...

The Executive Director, Global Regulatory Affairs Therapeutic Area Leader- GTAL provides strategic oversight and direction for regulatory activities on a global and/or regional scale across one or mor...

We are seeking an experienced and highly motivated Associate Director, Regulatory Affairs to support our expanding portfolio in the oncology area. Minimum of 5 years of regulatory affairs experience i...

More Years in regulatory affairs; experience in US regulatory affairs from IND through NDA/BLA required. This role will be accountable for ensuring consistent and transparent ways of working across th...

More Years in regulatory affairs; experience in US regulatory affairs from IND through NDA/BLA required. This role will be accountable for ensuring consistent and transparent ways of working across th...

Regulatory Advertising & Promotion Policy, Adpromo, Ad Promo, Regulatory Affairs, RAC, PharmD, Scientist, Technical Writer, Labeling, RA, Reg. Associate Director of Regulatory Affairs - Ad Promo. Soli...

Solid foundation in ad/promo regulatory affairs, with a total of 7 years in Pharma Regulatory. Regulatory Advertising & Promotion Policy, Adpromo, Ad Promo, Regulatory Affairs, RAC, PharmD, Scientist,...

The Executive Director, Regulatory Affairs will provide leadership and direction for the global regulatory aspects of Eisai's products under development and post approval research, including the devel...

The Executive Director, Regulatory Affairs will provide leadership and direction for the global regulatory aspects of Eisai's products under development and post approval research, including the devel...

The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executes multidivisi...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

As our project portfolio at Genmab continues to grow, we are expanding our team and seeking a Team Lead, Associate Director to join the Regulatory Affairs CMC (RA CMC) team. We offer an exciting and c...

As our project portfolio at Genmab continues to grow, we are expanding our team and seeking a Team Lead, Associate Director to join the Regulatory Affairs CMC (RA CMC) team. We offer an exciting and c...

Responsibilities include developing and implementing regulatory global strategy, driving regulatory submissions, fostering collaboration with regional colleagues, regulatory authorities and shaping/dr...

Responsibilities include developing and implementing regulatory global strategy, driving regulatory submissions, fostering collaboration with regional colleagues, regulatory authorities and shaping/dr...

Extensive hands-on experience in the development of key regulatory submissions, including NDAs, BLAs, MAAs, and INDs, as well as interacting with regulatory authorities and supporting site/sponsor reg...

Regulatory Affairs Certified is a plus. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. BS/BA in Life Sciences i...

Regulatory Affairs Certified is a plus. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. BS/BA in Life Sciences i...

Extensive hands-on experience in the development of key regulatory submissions, including NDAs, BLAs, MAAs, and INDs, as well as interacting with regulatory authorities and supporting site/sponsor reg...

Coordinates developing and implementing regulatory strategies for promotion and advertising plans, and is a leader in the Medical, Legal, and Regulatory Review process to support approval and dissemin...

Targeting 10 years of progressively responsible Regulatory Affairs experience focusing on advertising and promotional regulations. Coordinates developing and implementing regulatory strategies for pro...

More Years in regulatory affairs; experience in US regulatory affairs from IND through NDA/BLA required. This role will be accountable for ensuring consistent and transparent ways of working across th...

More Years in regulatory affairs; experience in US regulatory affairs from IND through NDA/BLA required. This role will be accountable for ensuring consistent and transparent ways of working across th...

Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Dem...