- Merck & Co. (Rahway, NJ)
- … products.Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and ... characterization such that the process is scalable without compromising stability, safety , efficacy, and delivery. During development, we leverage smart experimental… more
- Merck & Co. (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career.-- Director ( Principal Scientist ) has primary responsibility for the planning and ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal… more
- Merck & Co. (Rahway, NJ)
- …vaccines for the benefit of patients and global human health. The Associate Principal Scientist , Clinical Trial Analysis and Reporting leads the statistical ... programming activities for multiple and/or large/complex late stage drug /vaccine clinical development projects.- Accountability predominantly includes the development… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in… more
- Merck & Co. (Rahway, NJ)
- …and breadth of scientific and technical experience to lead small molecule drug substance process development teams to develop safe, robust and productive processes, ... suppliers.-- The engineer will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices… more
- Merck & Co. (Rahway, NJ)
- …suppliers.-- The engineer will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices ... management skillsPreferred Experience and Skills: Direct experience with pharmaceutical drug substance developmentFamiliarity with concepts and application of cGMP… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Director ( Principal Scientist ) has primary responsibility for planning and directing clinical research activities involving ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal… more
- Merck (Rahway, NJ)
- …products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and ... characterization such that the process is scalable without compromising stability, safety , efficacy, and delivery. During development, we leverage smart experimental… more
- Merck (Rahway, NJ)
- …colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publication; and +… more
- Merck (Rahway, NJ)
- …vaccines for the benefit of patients and global human health. The Associate Principal Scientist , Clinical Trial Analysis and Reporting leads the statistical ... programming activities for multiple and/or large/complex late stage drug /vaccine clinical development projects. Accountability predominantly includes the development… more
- Merck (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career. Director ( Principal Scientist ) has primary responsibility for the planning and ... the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug... safety and efficacy as well as new drug applications, clinical study reports, or publication + Participation… more
- Merck (Rahway, NJ)
- …and breadth of scientific and technical experience to lead small molecule drug substance process development teams to develop safe, robust and productive processes, ... suppliers. The engineer will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices… more
- Merck (Rahway, NJ)
- …statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. Accountability predominantly includes the development ... and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of which range from… more
- Merck (Rahway, NJ)
- …suppliers. The engineer will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices ... skills **Preferred Experience and Skills:** + Direct experience with pharmaceutical drug substance development + Familiarity with concepts and application of cGMP… more
- Fresenius Medical Center (Rockleigh, NJ)
- …patient results in collaboration with the Lead, Supervisor or Manager. ** PRINCIPAL DUTIES AND RESPONSIBILITIES:** + Under close supervision acquires job skills ... + Resolves instrumentation and methodology issues. + Complies with all laboratory safety protocols, including, but not limited to, the use of personal protective… more
- Pfizer (Pearl River, NY)
- …clinical components of documents (eg, Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy ... expertise to steer clinician medical monitors, clinician clinical scientists, clinical scientist leads, and other clinical staff members. The clinician medical… more
- Pfizer (Pearl River, NY)
- …approval for a compound or group of compounds. **ROLE RESPONSIBILITIES** **Accountable for safety across the study:** + Provide study team with medical advice for ... and mitigation planning to enable quality, compliance and patient safety at the trial, site and patient level. +...monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of… more
- Pfizer (Pearl River, NY)
- …delivery and reporting of one or more clinical studies and to ensure patient safety . + The clinician medical monitor may be required to design a development strategy ... accountability and level of judgment required. **ROLE RESPONSIBILITIES** **Accountable for safety across the study:** + Provide study team with medical advice… more
- Bristol Myers Squibb (Madison, NJ)
- …the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) + Holds responsibility for assessment of key safety ... organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution,… more