- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex- ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and transparent ways of working across the Alliance within US regulatory affairs and will work closely… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Qualifications7 or More Years in the pharmaceutical industry4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA Travel Ability to travel up to 30%… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... into the Oncology drug development preferred.Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including CCDS and US /EU labeling experience ... pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experienceExperience with ex- US… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including CCDS and US /EU labeling experience ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services, ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...the business functions of Daiichi Sankyo (DS) in the US , EU, Japan, and other global sites. These business… more
- Bayer (Whippany, NJ)
- …diverse minds to make a real difference, there's only one choice.** **Associate Medical Director , US Medical Affairs Oncology, Prostate Cancer** As a ... primary responsibilities of this role, Associate Medical Director , US Medical Affairs...to verify identity and eligibility to work in the United States and to complete the required… more
- Bayer (Whippany, NJ)
- …and diverse minds to make a real difference, there's only one choice.** ** Medical Director , US Medical Affairs Oncology, NUBEQA** As a key member ... of the US Medical Affairs Oncology team, the Medical Director...to verify identity and eligibility to work in the United States and to complete the required… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …possible, together. **Job Description** The Director of Business Intelligence, for Medical Affairs will serve as a player/coach to lead the development ... analytics, and field operations, with a strong understanding of medical affairs in the life sciences industry....conditions of the applicable plans. **For jobs in the United States :** As an equal opportunity employer,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …, Global R&D and Business Development Date: Jan 15, 2025 Location: Parsippany, United States , New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 60132 ... to make a difference with. **The opportunity** The Senior Director , Head of Corporate Affairs , Global R&D...and influence of Head of Global R&D and Chief Medical Officer, Head of Business Development and senior R&D… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and transparent ways of working across the Alliance within US regulatory affairs and will work closely… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …to the terms and conditions of the applicable plans. **For jobs in the United States :** As an equal opportunity employer, Gilead Sciences Inc. is committed ... 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… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory...industry required. + 8 or More Years in regulatory affairs + Experience in providing regulatory strategic input into… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory...industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... 7 or More Years in the pharmaceutical industry + 4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA **Travel** Ability to travel up to 30% In-house… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience with ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs + Knowledge of IND, NDA/BLA submission experience + Experience with… more
