- Merck & Co. (Rahway, NJ)
- …acts as primary site contact and site manager-throughout all phases of a clinical research study, taking responsibility of allocated sites.Develops strong site ... to present technical information with support.Good understanding and working knowledge of clinical research , phases of clinical -trials, current GCP/ICH &… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...percent of the time to manage future or ongoing clinical research projects. Qualifications Education MD, DO,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary:This position ... will be a member of the Risk Management Center of Excellence office who will help manage risk management initiatives and activities defined by leadership. Individual will provide strategic advice, teachings, and support related to risk management planning,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThis position supports ... safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director, Clinical Operations may act as the Study Team ... methods and processes in industry setting. required Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical… more
- Merck & Co. (Rahway, NJ)
- …maintenance of statistical databases that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The ... Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug/vaccine clinical … more
- Merck & Co. (Rahway, NJ)
- …scientists to ship samples both domestically and internationally in support of various research programs.The Associate Specialist will also be expected to lead ... Job Description Position Description: Associate Specialist - Operations Support The Enabling Facilities...The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …operations methods and processes in industry setting required.Experience considered relevant includes clinical or basic research in a pharmaceutical company, a ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThis is an ... projects and/or identification of issues which may compromise patient dosing or safety . Basic understanding of professional working environment as well as Quality… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary This position… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …scientific journalsAssess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease ... strategy for assigned products. Collaborate with epidemiology colleagues and Product Safety Lead to identify research gaps, develop protocols, conduct… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The purpose ... develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual ... and project management responsibility. The Specialist -Engineering position will report to the Associate Director, Engineering and will be a member of the EF Team at… more
- Merck & Co. (Rahway, NJ)
- …regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Primary activities include, ... but are not limited to:Reports to Executive Director or Associate Vice President, Therapeutic Area Lead.Develops worldwide product regulatory strategy to optimize… more
- The Mount Sinai Health System (New York, NY)
- The Clinical Research Associate is an...all safety aspects of clinical research trial(s). Under guidance of the Associate Director ... for collecting, assessing and processing Adverse Events (SAE) for safety reporting, CEC and DSMB of clinical ...in all aspects of patient care delivery, education, and research to promote policies and practices to allow opportunities… more
- Merck (Rahway, NJ)
- …acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. + Develops strong ... site are complete, accurate and unbiased o Subjects' right, safety and well-being are protected + Conducts site visits...with support. + Good understanding and working knowledge of clinical research , phases of clinical … more
- Pfizer (Pearl River, NY)
- …EudraCT, or Pfizer.com) + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with ... Program team, interfaces with discovery, safety sciences, statistics, clinical pharmacology, commercial, regulatory, outcomes research , Global Product… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... mission to transform healthcare and serve as a leader ofpositive change. The Clinical Research Nurse is responsible for coordinating and overseeing clinical… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The Clinical Research Nurse is responsible for coordinating...Together with the principal investigator, reviews and processes all Safety Reports (INDs, SUGARs) as per institutional policies and… more
- L'Oreal USA (Clark, NJ)
- … Associate Principal Scientist, Advertising Claims Substantiation, L'Oreal Research & Innovation Clark, NJ, New Jersey Apply now ... Substantiation to join our Claims Substantiation team in our Clark, New Jersey Research facility. As an Associate Principal Scientist in our Claims… more
