- Merck & Co. (North Wales, PA)
- …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. (Rahway, NJ)
- …- #eligibleforERP GCSCareer25 #PSCSRequired Skills: Adaptability, Change Management, Clinical Research , Cross-Functional Team Leadership, Data Analysis, ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company Research Laboratories portfolio of… more
- Merck & Co. (Rahway, NJ)
- …support to the marketing groups for key molecules/products and clinical research expertise upon request.Conducts post-marketing studies.Prepares scientific ... of GCP Good Clinical Practices guidelines.Competencies Required: Four years in clinical research or similar research role.Experience in a … 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. (MA)
- …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
- Merck & Co. (Rahway, NJ)
- … Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Company's Research and Development ... operational/executional arms within the business.- - Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and… more
- Merck & Co. (Upper Gwynedd, PA)
- …--The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director ... has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …economics, epidemiology, outcomes research , public health, health services research , biostatistics, medicine, clinical research , biomedical sciences) ... About the Department The Clinical , Medical and Regulatory (CMR) department...a minimum of 4 years of experience in similar clinical /medical/ research departments in Pharmaceutical Industry, in health… 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
- 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
- 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
- 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
- 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
- Merck & Co. (Rahway, NJ)
- …Medical, Data Coordination, Statistical Programming, Research Laboratories scientists and Regulatory staffs in designing and analyzing clinical trials and ... Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our...communicate results of clinical trials to the project team, Management, regulatory agencies, or individual… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …medical affairs, and regulatory affairs Maintain training assignments on clinical research documentation, regulatory requirements, Good Clinical ... global regulatory requirements Coordinate mandatory compliance training for clinical research staff, including GCP certification and recertification programs… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the programming standards and practices, SOPs, external/internal data standards, Good Clinical Practices (GCPs), applicable regulatory requirements, and other ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: The… more
- Merck & Co. (Rahway, NJ)
- …Algorithms, Applied Mathematics, Biostatistics, Business Process Improvements, Business Strategies, Clinical Development, Clinical Research , Clinical ... datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing… more
- Merck & Co. (Rahway, NJ)
- …in mammalian cell culture or purification process development, tech transfer of clinical or/and commercial processes, and pertinent regulatory filings. The ... The Director, Biologics Process Development (BPD) within the Biologics Process Research and Development (BPR&D) organization is responsible for designing and… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.-The position is… more
