- AbbVie (Florham Park, NJ)
- …as they relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions. + Provide scientific /medical ... strategy. + Must possess excellent oral and written English communication skills. Scientific Director Qualifications: + Advanced Degree PhD or PharmD. Additional… more
- AbbVie (Florham Park, NJ)
- …internally to support business strategy. International experience is a plus. Senior Scientific Director Qualifications: + Advanced Degree PhD or PharmD. ... title will be based on qualifications listed below. Purpose: The Senior Director provides specialist medical and scientific strategic and operational input… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** Regulatory Affairs Global Labeling is a core function within Gilead's ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...Global Regulatory Affairs organization and acts as a… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …regardless of where they live or their economic status. **POSITION OVERVIEW:** As a Director , Early Oncology Global Regulatory Affairs , you will develop and ... role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. You will also help develop the TA's … more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Director , US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge, MA or Morristown, NJ **About the job** Are you ready to ... and direct reports. + In conjunction with the Sr. Director /Product Support Head, imparts senior regulatory guidance...8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record of… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …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 ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience… more
- Bausch Health (Bridgewater, NJ)
- …CCDS and USPI documents for new products. + Solid understanding of pharmaceutical regulatory affairs , global labeling regulatory requirements and industry ... skills and values drive our collective progress and impact. The Global Labeling Director provides regulatory expertise and guidance for labeling strategy, to… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …including working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...& variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + Provides scientific /medical education to investigators, clinical ... Job Title Director , Clinical Development and Medical Affairs ...with other internal stakeholders including clinical operations, statistics and regulatory . + Provides scientific and technical support… more
- Bristol Myers Squibb (Madison, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more