- Daiichi Sankyo, Inc. (Bernards, NJ)
- …issues with regard to ways or working or resources to the Head of US Regulatory Affairs and/or Global Regulatory Lead for asset to reach ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi... global product team meetings to provide US regulatory support and guidance as needed and manage day-to-day… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical/oncology project development preferred- 1 or More Years Extensive knowledge of global CMC regulatory requirement and preferably NDA or BLA/MAA ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...of the project. The CMC Lead will support the Sr . CMC Lead on complex and/or late-stage project or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality standards and timelines and that quality of data is suitable for regulatory submission.The Associate Director will have routine interaction with key ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...and share with study team, Operations Program Lead, and Sr . Director for the compound, on regular… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Sr Director , Global Regulatory Medical...a difference with. **The opportunity** The Senior Director in Global Regulatory Medical ... marketing to meet the company's global strategic, scientific, regulatory , and commercial goals. The Senior Director will also: + offer clear leadership… more
- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson is currently seeking a Senior Director , Regulatory Affairs Global Strategy Implementation to join our team preferably located in ... At Johnson & Johnson, we all belong. The Senior Director , Regulatory Affairs Global Strategy Implementation partners with MedTech Surgery business… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …and demand integrity and respect in all we do, create and deliver. Senior Director , Intellectual Property Counsel will be an experienced biopharmaceutical IP ... origin, protected veteran status, disability or any other legally protected status. Sr . Director , Intellectual Property Counsel Salary Range: $260K - $300K… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …implementation plans to support product development or market access objectives in a global organization. The Senior Director provides expertise and guidance ... industry standards + Extensive experience in preparing and participating in global regulatory agency interactions + Demonstrate excellent collaboration,… more
- SHI (Somerset, NJ)
- …manner, providing expert insight and industry-leading knowledge. The position reports to the Global Director ITAM Services. The Senior Manager-ITAM BMO will ... **Job Summary** The Senior Manager - ITAM Business Management Office (BMO)...also have the responsibility & authority to manage the regulatory & compliance programs required by SHI and the… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to ... support global registration and commercialization of Gilead's products. This position...+ In partnership with Clinical Program Manager or Associate Director , provides guidance and daily oversight for the successful… more
- System One (Florham Park, NJ)
- …Research, review, and/or assess potential CROs and vendors in collaboration with the Director and other colleagues based on needs. + Work with Clinical Development ... other functions globally (Biometrics team (Data Management, Programming, and Statistics), Regulatory , Drug Safety, and other functions) on supporting all applicable… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Brings issues with regard to ways or working or resources to the Head of US Regulatory Affairs and/or Global Regulatory Lead for asset to reach resolution. + ... Participate in global product team meetings to provide US regulatory support and guidance as needed and manage day-to-day regulatory activities. + Continuing… more
- Sanofi Group (Morristown, NJ)
- ** Global Commercial Switch Lead** + Location: Morristown, NJ **_About the Job_** At Sanofi Consumer Healthcare, we build trusted and loved brands that connect with ... the best fast-moving consumer healthcare company in and for the world. The Global Commercial Lead for Switch is responsible for driving the pre-commercialization and… more
- Sanofi Group (Morristown, NJ)
- ** Global Commercial Switch Lead** + Location: Morristown, NJ **_About the Job_** At Sanofi Consumer Healthcare, we build trusted and loved brands that connect with ... the best fast-moving consumer healthcare company in and for the world. The Global Commercial Lead for Switch is responsible for driving the pre-commercialization and… more
- Sanofi Group (Bridgewater, NJ)
- **Job Title** : Global Director of Communications for Hemophilia **Location:** Cambridge, MA **About the Job** Sanofi is seeking a strategic, motivated, and ... experienced communications professional for the position of Global Director of Communications for Hemophilia, part of the Rare Diseases Franchise. This position… more
- System One (Florham Park, NJ)
- Job Title: Director / Senior Director , Medical Operational Excellence Lead Full time permanent position - Direct with a global pharmaceutical company ... + Minimum of 8 -10 years ( Director ) or, minimum 10-12 years ( Senior Director ) of experience in medical operations, clinical operations, or a related… more
- Sanofi Group (Bridgewater, NJ)
- **Job title** : Associate Director , Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty Care... communications programming in support of clinical data and regulatory milestones as well as pipeline; 2) supporting development… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Director , Supply Chain CBMSO Planning Lead Date: Dec 30, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... Lead is overall accountable for the effective operation, execution, deployment of global methodology and coordination of the Supply Chain Function in the segment.… more
- Bausch Health (Bridgewater, NJ)
- …it-where your skills and values drive our collective progress and impact. As a Senior Director in Health Economics and Outcomes Research (HEOR), you will be ... Join a team! We are a global diversified pharmaceutical company enriching lives through our...matrix leadership teams + Thorough understanding of industry and regulatory guidelines as they relate to HEOR and Medical… more
