- Eisai, Inc (Nutley, NJ)
- …May provide training on GCP and current regulations for those undertaking clinical studies.Job SummaryThe Associate Director , GCP Quality Assurance works within ... 25%)Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Quality Assurance is from :159,500-209,400Under current… more
- Merck & Co. (Rahway, NJ)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire ... execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...the PositionAs Formation Bio's dedicated IP Counsel at the Director level, you will own the IP function for… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The… more
- Merck & Co. (Rahway, NJ)
- …and will interact externally with key opinion leaders.-Specifically, the Executive Director may be responsible for:Evaluating pre- clinical and translational work ... opportunities.Managing other Directors and/or Senior Directors responsible for Atherosclerosis clinical development projectsThe Executive Director may supervise… more
- Daiichi Sankyo, Inc. (New York, NY)
- …company in a positive and professional manner. Reporting to the Regional Business Director , oversee the promotion of the assigned products consistent with the FDA ... hospitals, and community practices).Demonstrate understanding of current or pending clinical pathways in assigned accounts, and how they influence patient… more
- Merck & Co. (Rahway, NJ)
- … clinical implementation and advancing digital pathology within our company's clinical therapeutic pipeline.The Principal Scientist ( Director ) will have the ... Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
- Merck & Co. (Rahway, NJ)
- …is to provide statistical support for the pharmacology components of all clinical trials in our Company's Research Laboratories clinical development pipeline. ... in scope prior to an asset's potential advancement to late stage clinical development are proof of biology/concept clinical trials, experimental/discovery… more
- Merck & Co. (Rahway, NJ)
- …the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical ... Job DescriptionJob Description Director -QP2-IO We are seeking an experienced talented scientist to join the - Quantitative Pharmacology and Pharmacometrics - -… more
- Merck & Co. (Rahway, NJ)
- …drive pipeline impact and lead a talented group of pharmacometricians.This Senior Director is expected to be an experienced pharmacometrician with a strong, ... to strengthen our pharmacometrics capabilities on a continuous basis. The Senior Director will be accountable for directing a team of pharmacometricians with diverse… more
- Merck & Co. (Rahway, NJ)
- …role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with… more
- Merck & Co. (Rahway, NJ)
- …at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director / Principal Scientist, Regulatory Affairs Liaison , is responsible for the development and implementation of worldwide regulatory strategy ... regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Key functions:Reports to Senior… more
- Merck & Co. (Rahway, NJ)
- …the guidance of a senior leader, an Associate Principal Scientist/Associate Director , has primary responsibility for planning/managing real world and economic ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- …are seeking a highly skilled and motivated Associate Principal Scientist/Associate Director with expertise in conducting outcome researching using real world data, ... models to extract meaningful insights and outcome research evidence. Unstructured Clinical Data: Utilize transfer learning, fine tuning, GAN, transformer, attention,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... Systems, Business, Capital Project Management, Change Management, Chemical Manufacturing, Clinical Manufacturing, Compliance Reviews, Data Analysis, Decision Making, Drug… more
- Merck & Co. (Rahway, NJ)
- …SummaryUnder the guidance of a senior leader, a Principal Scientist/ Director , has primary responsibility for developing value evidence strategies, and ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting to the Executive Director , RIIM , this role will be accountable to ensure a holistic Regulatory centric D ata M anagement ( R DM) capability ... for GRACS and other critical stakeholder areas including PV, Clinical and Supply Chain to ensure that datasets are...c ross functional Leaders is critical. Th e Senior Director should have strong managerial experience, a high-level strategic… more
