- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for Associate Director , RA Submissions . The position can be located on-site/hybrid in the US ... with dossier level publishing partners to achieve production of regulatory submissions that conform to regional and...equivalent experience in a related field (Pharmacy, Life Sciences, Regulatory Affairs , etc.) + A minimum of… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and Promotion ( RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... biologic products. + Significant experience leading development and execution of regulatory submissions of promotional materials for marketed prescription drug… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Strategy Princeton, NJ, USA Req #415 Wednesday, November 27, 2024 Looking for a chance to make a meaningful ... Abilities: + Ten years previous experience in global regulatory affairs and regulatory submissions for drugs, preferably experience in oncology. + Five… more
- Sumitomo Pharma (Trenton, NJ)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs ** . The ... Director is part of the Global Regulatory Affairs (GRA) team based in the...perseverance to achieve results + Experience contributing to electronic regulatory submissions and working with regulatory… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …plans. 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 ,...pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …The Associate II (A), assists with minimal guidance, the Senior Director of Regulatory Affairs Clinical/ FDA Communications.Assists the Senior ... Director of Regulatory Affairs / Clinical Affairs in...+ Assist in reviewing and ensuring standards for eCTD submissions + Manage and maintain the In Vitro Task… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 ... TAU within our Global Regulatory Affairs organization, based remotely. + Partners..., to oversee, plan and deliver GRT goals and regulatory submissions in accordance with regulatory… more