- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. ... clinical study reports, or publication;Participation in internal and joint internal/external research project teams relevant to the development of new… more
- Merck & Co. (Boston, MA)
- …(Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... clinical study reports, or publicationParticipation in internal and joint internal/external research project teams relevant to the development of new… more
- Merck & Co. (South San Francisco, CA)
- …Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. ... study reports, or publication; andParticipation in internal and joint internal/external research project teams relevant to the development of new compoundsThe… more
- Eisai, Inc (Nutley, NJ)
- …years of pharmaceutical industry related experience as a Clinical Pharmacology Project Lead.A thorough understanding of global regulatory requirements on the ... the experience and conviction to provide sound input on Clinical Pharmacology activities to a variety of project...data as it relates to safety and efficacy.Contributes to Clinical Pharmacology expertise and content to regulatory … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory , Project Management, Biostatistics, Pharmacology, and other ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Under the Group's… 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 ... responsibility you will provide strategic input to and monitor the execution of clinical studies as a project physician.Your ability to understand and navigate… more
- Genmab (NJ)
- …using R to support clinical trial preferred Demonstrated knowledge of clinical research , metadata management, industry standards (CDISC), FDA & ICH, GCP, ... Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and integrity of Study Data… more
- Eisai, Inc (Nutley, NJ)
- …on clinical quality topics.Build and manage overall relationships with regulatory bodies to address emerging needs and issues.Manage and retain talent within ... 15 or more years significant clinical pharmaceutical experience (ie, clinical development or operations, regulatory compliance).Substantial experience in … more
- Insmed Incorporated (NJ)
- …Analytical Development, Quality Assurance, and Regulatory , with input from Commercial, Research , and Clinical .Prepare and manage detailed project plans ... key functional areas throughout all stages of product development, including Research , Preclinical, Clinical , Regulatory , Operations, Quality… more
- BeOne Medicines (San Mateo, CA)
- …the Pharma R&D value chain. By collaborating with stakeholders across Research , Clinical , Safety, Regulatory , Portfolio & Project Management and other ... data products that address critical R&D use cases (eg, portfolio insights, clinical trial optimization, regulatory intelligence). + Establish best practices for… more
