- Merck (Trenton, NJ)
- …and Clinical Safety (GRACS) and external to GRACS. **Key functions:** + Reports to Senior Principal Scientist ( Senior Director) and/or Distinguished ... **Job Description** The Director/ Principal Scientist , Regulatory Affairs Liaison, is responsible for the development and implementation of worldwide regulatory… more
- Insight Global (Lower Gwynedd, PA)
- Job Description Our large pharmaceutical client is seeking a Sr . Principal Scientist , Cellular & Mechanistic Pharmacology to join as a direct FTE in Spring ... from target identification to clinical development. We're looking for a talented scientist with an immunology background, deep expertise in disease biology and… more
- Merck (North Wales, PA)
- **Job Description** The Senior Director ( Senior Principal Scientist ) has primary responsibility for the planning and directing clinical research ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development, including… more
- J&J Family of Companies (Titusville, NJ)
- …of America **Job Description:** We are searching for the best talent for a ** Senior Principal Scientist , Technology Innovation, Commercial Data Science** to ... be in Titusville, NJ. Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in… 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 ... for model development Requirements: + Have substantial experience in a senior data scientist role + Have experience in leading complex projects and customer… more
- Bristol Myers Squibb (Princeton, NJ)
- …cancer biology, human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr . Principal Level (and minimum of 8 years Post-PhD experience for AD ... Level), with demonstrated scientific leadership in integrating, analyzing, and interpreting multimodal biological data in an academic and/or industry setting. + Strong background in human genetics/genomics, cellular biology, immunology or immuno-oncology, with… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Develops and executes translational disease strategy in the pancreatic cancer (PC) area with deep disease expertise + Leads and oversees execution of disease ... strategy including but not limited to various aspects of patient selection strategies + Serves as scientific expert in generating novel hypotheses for actionable biology based on novel discoveries integrating disease work with literature and deep expertise in… more
- Merck (West Point, PA)
- …regulatory submissions. Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with internal and ... external partners, this person will support mid-late stage and commercial cell bank-related projects for large molecule programs. The person will be responsible for commercialization activities on late-stage pipeline and/ or post-market commercial… more
- Merck (North Wales, PA)
- **Job Description** **Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility ... for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. + Types of studies executed… more
- Bristol Myers Squibb (Princeton, NJ)
- …Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management ... non-significant deviations etc.) + Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to… more
- Bristol Myers Squibb (Princeton, NJ)
- …acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more
- Bristol Myers Squibb (Princeton, NJ)
- …on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... lifecycle + Manages site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)… more