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Call Whether it s dock-to-dock delivery, our customers know that there is one name to trust with the logistics of their high value products and we need the BEST. CDL A Driver Out 3 Weeks We are a rapidly expanding company based in Cincinnati, OH and...
Reporting to a Vice President of Regulatory Affairs, the Manager will support day-to-day regulatory activities of assigned projects. These include support of preparation and compilation of submissions for regulatory agencies, assigned clinical studies,...
BridgeBio ultimately exists to help patients. Millions worldwide are afflicted with genetic diseases, but small patient populations and industry reluctance to conduct early-stage development means that for many, treatments have not been forthcoming. We...
Associate/Associate Director of Asset Acquisition This position will help set the culture and business development for BridgeBio, will be the face of the organization, and will be a critically important player in building and maintaining BridgeBio's...
The Senior Clinical Scientist will play a supportive role in clinical development of infigratinib for oncology and potentially non-oncology indications. Working in collaboration with Clinical Development, the position is responsible for various aspects...
Manager/Senior Manager, Regulatory Affairs The candidate will have demonstrated the ability to work independently or with limited oversight. Furthermore, the candidate will have demonstrated knowledge of regulatory requirements and guidelines and the...
This experienced regulatory professional will develop and implement regulatory strategy for internal development programs. In addition, the individual will implement and manage internal regulatory processes, prepare documents for regulatory submissions...
We are looking for two Medical Science Liaisons (MSLs) to serve one of two territories: (East and West). The Eidos MSL is responsible for liaising with a variety of internal and external customers and providing medical and scientific information on the...
The Senior Medical Writer develops, writes, and edits clinical/regulatory documents (such as clinical study reports [CSRs], clinical protocols, investigator brochures, regulatory briefing documents, and CTD Module 2 summaries), both independently and...
The Medical Director, Pharmacovigilance serves as the product safety lead for assigned study/product, and are accountable for executing the safety and risk management activities of assigned clinical development projects/marketed product to enable the...