- Merck (North Wales, PA)
- **Job Description** **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and ... implementation of worldwide regulatory strategy for their assigned projects in the General...functions with a high degree of independence and provides regulatory oversight for assigned products, to optimize product labeling… more
- Merck (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist ) has primary responsibility ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director… more
- Bristol Myers Squibb (Princeton, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Senior Principal Scientist - DMPK Project Representative When you ... pharmacokinetics activities of multiple projects; be responsible for preparation of regulatory dossier/responses; and assist in developing strategy for the group.… more
- RELX INC (Trenton, NJ)
- Principal Data Scientist I Are you looking to...for our customers and communities. About the Role: As a Senior Data Scientist , you will become a subject ... of RELX, is a leading global provider of legal, regulatory , and business information. We help customers increase productivity...model development Requirements: + Have substantial experience in a senior data scientist role + Have experience… more
- Endo International (Horsham, PA)
- …for talented individuals to join our team. **Job Description Summary** The Principal Scientist , Laboratory Technical Services is primarily responsible for ... company goals and initiatives and is considered an SME for these areas. The Principal Scientist is responsible for planning, designing, and execution of LTS… more
- Merck (North Wales, PA)
- …and dedicated colleagues while developing and expanding your career. The Director ( Principal Scientist ) has primary responsibility for the planning and directing ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may be… more
- Merck (West Point, PA)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** + Lead and set direction for the device… more
- J&J Family of Companies (Titusville, NJ)
- …data sources across multiple disease areas. We are looking for outstanding scientist and leader whose responsibilities include: + Be a hands-on technical leader, ... RCT analyses, observational databases, and literature reviews to support regulatory agency interactions. + Independently create study protocols, statistical analysis… more
- Merck (North Wales, PA)
- …colleagues while developing and expanding your career. **The Senior Director ( Senior Principal Scientist )** has primary responsibility for the planning ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Senior Clinical Trial Physician, (Late Clinical Development, Cell Therapy, ... Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management… more
- Novo Nordisk (Plainsboro, NJ)
- …late-stage clinical development. We are building a multi-talented team of physician scientist drug developers that works together to tackle key challenges and ... therapeutic area, help develop PRO and biomarker strategies. Relationships Reports to: Senior Director of the Liver Disease department. Work with the Clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more