- Bristol Myers Squibb (Princeton, NJ)
- …of high-quality scientific publications in relevant fields The starting compensation for Senior Scientist is a range from $112,000- $140,000, plus incentive ... facilitates the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage translational… more
- Merck (Rahway, NJ)
- …PK modeling and simulation stakeholders spanning all therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the required ... or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, Life… more
- Taiho Oncology (Princeton, NJ)
- …to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist , you will play a pivotal ... at the forefront of cancer research. Position Summary: The Senior Manager, Clinical Research Scientist ...in design, execution and reporting of current and future clinical oncology trials ranging from phase 1… more
- Bristol Myers Squibb (Princeton, NJ)
- …facilitates the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage translational ... the development, and maximize the potential, of BMS's therapies post- clinical proof-of-concept, including registrations and life-cycle management. Translational disease… more
- Merck (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist ) has primary ... responsibility for the planning and directing clinical research activities involving new Oncology medicines...medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck (Rahway, NJ)
- …and PK/PD Modeling and Simulation spanning all therapeutic areas except early oncology . + Gather and interpret user requirements for programming requests, retrieve ... field plus 3 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 5 years SAS programming experience in a clinical trial environment. **Minimum requirement:** + Must have experience… more
- Merck (Rahway, NJ)
- …execute statistical analysis and reporting deliverables under the guidance of a senior -level programmer supporting early-phase oncology clinical trials. ... well as stakeholders in data management, medical writing, and clinical operations to gather and document requirements for statistical...and complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate… more
- Merck (Rahway, NJ)
- …company's innovations and improve patient health outcomes. Under the guidance of a senior leader, this individual will support the V&I, Outcomes Research teams in ... market access in collaboration with internal teams, and provide input into clinical , payer/access, marketing and value evidence generation strategies and programs. +… more
- J&J Family of Companies (Titusville, NJ)
- …team within Johnson and Johnson Innovative Medicines is looking for an outstanding scientist and leader who provides cross therapeutic area RWE expertise and whose ... from data feasibility, study design and analysis, to final presentation to senior cross-functional leaders. + Partner with the Data Science Therapeutic Area leaders… more