- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist will represent Regulatory Affairs within the Worldwide Infusion Preparation and Delivery ... MDR, and other global regulatory filings. + Evaluate medical device regulations and lead the development of global regulatory strategies to bring products to market.… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or ... activities for all assigned projects in alignment with the Global Regulatory Lead . Translates complex pertinent global requirements and provides an assessment of the… more
- Axtria, Inc. (Berkeley Heights, NJ)
- …and evidence synthesis strategies that inform client objectives-including market access and clinical decision-making. Key Responsibilities + Lead and support the ... About Axtria Axtria is a global leader in cloud software and data analytics for...and Generative AI (GenAI) tools that automate complex forecasting, clinical reporting, and patient segmentation with unprecedented speed and… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Senior Manager, EHSS Systems Implementation is accountable for operational ... EHSS Performance & Systems Innovation and cross-functional partners, the Senior Manager supports EHSS systems governance activities, continuous improvement,… more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... Us link on all NNI websites and the CC Outlook box + Project management- Coordinates department-wide projects and provides up to date information ensuring key… more
- Oracle (Trenton, NJ)
- **Job Description** As a Senior Software Engineer, you will work with Product/Design during the design phase, author a technical approach to building the features, ... technologies * Self-driven, able to work independently on a project even while the design is evolving * Strong...distributed teams * Experience in the healthcare industry and clinical applications is a plus Disclaimer: **Certain US customer… more
- Bristol Myers Squibb (Princeton, NJ)
- …and mastery in senior level competencies. + Experience in drug development project management at both the individual project level and across a portfolio ... largest BMS development portfolio including several priority assets. The ED PM Portfolio Lead is accountable for PM team member delivery per defined roles and… more
- Merck (Rahway, NJ)
- …concepts as applied to drug/vaccine development within the pharmaceutical industry; + A project leader ; completes tasks independently at a project level, ... determines approach and ensures consistency, manages timelines; ability to communicate clearly to key stakeholders + Ability to extend existing or develop new programming algorithms + Ability to quickly and effectively learn new program techniques and data… more
- Bristol Myers Squibb (Princeton, NJ)
- …of the organization. + In depth knowledge of overall project planning and project management of clinical trials + Proven ability to partner effectively with ... more: careers.bms.com/working-with-us . **Position Summary** The Medical Evidence Generation (MEG) Lead in Immunology & Neuroscience at Bristol Myers Squibb oversees… more
- Ascendis Pharma (Princeton, NJ)
- …compliance with regulatory standards. 2. Training Facilitation and Trainer Certification + Lead live and virtual training sessions for global Medical Affairs teams, ... 6. Cross-Functional Collaboration + Partner with cross-functional teams including Clinical Development, Regulatory Affairs, and Commercial to align training… more