- Bristol Myers Squibb (Summit, NJ)
- …issues or for continuous improvement programs. + Develop and deliver against project plans that support technical transfers, APS, new equipment installations. + ... errors within their WCT. **Process Expertise** + Supports Material Review Board (MRB) data collection and provides process expertise when required to support the MRB… more
- Bristol Myers Squibb (Princeton, NJ)
- …and approved by the 340B Working Group and Executive Committee, drive the project from ideation to execution. + Engages with internal and external stakeholders to ... the 340B working group and affiliated leadership updates and tracks cross-functional project activity across MAx, Legal and USPGA. + Leads the cross-functional… more
- J&J Family of Companies (Titusville, NJ)
- …Manager** **/Associate Director** , **Regulatory Medical Writing** within our Integrated Data Analytics & Reporting (IDAR) business. This role will support one ... of TA). + Preparing and finalizing all types of clinical documents, taking a proactive or lead role in...PhD preferred. + At least 10 years of relevant pharmaceutical /scientific experience; at least 8 years of relevant Medical… more
- AbbVie (Jersey City, NJ)
- …The Manager of Statistical Programming must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. ... team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for leading the statistical… more
- Sanofi Group (Morristown, NJ)
- …Real-World Evidence (RWE) that address critical evidence gaps and support clinical decision-making using existing platforms and through novel studies + **Translate ... equivalent advanced medical degree. **Work Experience** : + 5+ years of pharmaceutical industry experience in Medical Affairs + Demonstrated expertise in dermatology… more
- Bristol Myers Squibb (Princeton, NJ)
- …Coordinate with matrix team partners and conducts follow-ups as necessary to ensure project timelines are on track and milestones are being met + Proactively ... not required. + Minimum 5 years of relevant commercial experience in pharmaceutical or healthcare related industry required. + Position requires demonstrated … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …communicate data gaps, and work collaboratively with research teams ( Clinical Development, Medical Affairs Research, Value and Access Health Economic and ... a field PAQ MS external engagement strategy with US payers/HCDMs and clinical pathways/Oncology Care Management organizations to accomplish PAQ goals and objectives… more
- Taiho Oncology (Princeton, NJ)
- …complex data and support strategic decision-making. + Strong organizational, project , and time management skills, with the ability to prioritize, meet deadlines, ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ BA/BS required; MBA preferred + At least 5 - 7 years' pharmaceutical industry or related consulting experience in marketing and US market access area, ... effectively in complex, rapidly changing environments + Significant experience with strong project and process management skills, along with the ability to work on… more
- WTW (Short Hills, NJ)
- …of the life science landscape and the unique risks faced by pharmaceutical , biotech, and medical device companies. The CA will manage client relationships, ... comfortable working collaboratively across internal teams to deliver innovative, data -driven solutions. Note: Employment-based non-immigrant visa sponsorship and/or assistance… more