- Reckitt (Parsippany, NJ)
- Regulatory and Safety Affairs Associate City: Parsippany **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition ... to grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate , Regulatory and Compliance provides regulatory … more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs ** **Description** : The ... role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply...+ Proven aptitude to analyze and interpret efficacy and safety data + Experience communicating and negotiating with OPDP/APLB… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …of our day and improving the lives of patients for generations to come. As an Associate Director, Global Regulatory Affairs , you will act as the Regional ... role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. Position will be filled in either Foster City,… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …please visit Gilead.com. We have an exciting opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical ... experience inOncologyMedicalAffairs + Industry experience with knowledge of all applicable regulatory and legal requirements for Medical Affairs activities +… more
- AbbVie (Florham Park, NJ)
- …of work may include clinical trials, patient safety , and global medical affairs . The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , or GMA) to create development strategies for… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …study team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of...sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex… more
- Ascendis Pharma (Princeton, NJ)
- … Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA safety ... for employees to grow and develop their skills. The Associate Director, ICSR Management Team reports to the Director,... regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to 20%… more
- AbbVie (Florham Park, NJ)
- …of work may include clinical trials, patient safety , and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , and GMA, etc.) to create development… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5 more}… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more