- Merck & Co. (Rahway, NJ)
- … (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...percent of the time to manage future or ongoing clinical research projects.Qualifications Education MD or MD/Ph.D.Required… more
- Merck & Co. (Rahway, NJ)
- … (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the ... about twenty (20) percent of the time to manage future or ongoing clinical research projects.Education:M.D or MD/Ph.D.Required Experience and Skills:Minimum of 3… 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)
- …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)
- …Material(s):Required Skills:Adaptability, Adaptability, Business, Business Risks, Change Management, Clinical Development, Clinical Research , ... (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company Research... clinical supply chain across the full company Research Laboratories portfolio of clinical trials.- GCS… more
- Merck & Co. (Rahway, NJ)
- …clinical development across all therapeutic areas and all phases of clinical development at our company's Research Laboratories. Translational Molecular ... clinical implementation and advancing digital pathology within our company's clinical therapeutic pipeline.The Principal Scientist ( Director ) will have the… more
- Merck & Co. (Rahway, NJ)
- …of TMS is to provide statistical support for the pharmacology components of all clinical trials in our Company's Research Laboratories clinical development ... Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our...prior to an asset's potential advancement to late stage clinical development are proof of biology/concept clinical … more
- Merck & Co. (Rahway, NJ)
- …and statistical/survival analysis models to extract meaningful insights and outcome research evidence. Unstructured Clinical Data: Utilize transfer learning, ... as statistics, biostatistics, data science, biomedical informatics, health informatics, clinical informatics, epidemiology, health economics, biometrics, operations research… 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)
- …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)
- …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 DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... resolve manufacturing challenges and minimize supply disruptions. Collaborate with Research Laboratories groups during New Product Introductions/Technical Transfers and… 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)
- Job DescriptionThe Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a ... curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology...sci e ntis ts to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and… 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
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... write or facilitate the writing of key documents, with an emphasis on clinical development related documents within the Research & Development department. This… more
- Merck & Co. (Rahway, NJ)
- …global lawmakers on industry best practices and requirements for effective global clinical research .Co-lead our network of 250+ Global Privacy Stewards who ... Material(s):N/ARequired Skills:Business, Business, Business Consultations, Business Relationship Management (BRM), Clinical Judgment, Clinical Research , Compliance… more
- Merck & Co. (Rahway, NJ)
- …Data Modeling Tools, Data Visualization, Drug Development, Pharmacology Research , Pharmacometrics, Regulatory DocumentsPreferred Skills:C (Programming Language), ... Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Director , Quantitative Systems Pharmacology (QSP) . QP2-IO team is...(QSP) . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...the PositionAs Formation Bio's dedicated IP Counsel at the Director level, you will own the IP function for… more
