- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical ... existing and pipeline products to produce safe, effective, innovative medicine.The Clinical Director is responsible for protocol development and medical/ scientific… 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 our company ... Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (MA)
- … and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications .Providing clinical ... regarding safety and efficacy as well as new drug applications , clinical study reports, or publication; andParticipation...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Boston, MA)
- …clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications ;Developing ... regarding safety and efficacy as well as new drug applications , clinical study reports, or publicationParticipation in...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (North Wales, PA)
- …clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications ;Developing clinical ... regarding safety and efficacy as well as new drug applications , clinical study reports, or publication;Participation in...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Upper Gwynedd, PA)
- …to support decisions regarding safety and efficacy as well as new drug applications , clinical study reports, or publication; and participating in internal and ... report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… 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's Research and Development Division portfolio of clinical trials.- GCS is accountable for the planning, sourcing, labeling, packaging and delivery of … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their...###. This contact is for accommodation requests only and cannot be used to inquire about the status of applications… more
- Merck & Co. (Rahway, NJ)
- …and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of ... the candidate be responsible for the conduct of Good Clinical Practice (GCP) studies, and occasionally Good Laboratory Practice...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… 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 ... Research & Development Division portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Rahway, NJ)
- …Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers into clinical development across all therapeutic areas and all phases of ... clinical development at our Research & Development Division ....click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Genmab (NJ)
- …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 ... reporting and analysis standards, change control management and related tools/ applications Creates quality control processes, metrics and other measures to… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …and medical aspects of new respiratory medicines, including new drug or 505(b)(2) applications . This role involves strategic leadership in clinical trials, ... Regulatory Compliance: Ensure adherence to FDA guidelines for 505(b)(2) applications and other regulatory standards.Addressing medical/ clinical queries from… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with the Medical Monitor ... and cross functional teams. This individual will provide scientific support to clinical development and operations, regulatory and quality assurance teams, as well… more
- ALPCO (Denver, CO)
- …travel is required to install and maintain instrumentation, provide scientific applications support, train customers, and ensure clinical and research ... resource, providing insight into assay performance, diagnostic utility, and emerging applications in research and clinical diagnostics Support internal teams… more
- Aequor (Pearl River, LA)
- …in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities ... the world.ROLE SUMMARY We are seeking a highly motivated full-stack web application developer (contract) with exceptional programming skills to join Vaccines R&D in… more
- Lyra Health Inc (Jackson, MS)
- …North Carolina, Tennessee, Texas, and Washington. We will continue to welcome applications from all other states, and sponsor cross-licensure across selected states ... live video, maintaining a caseload of diverse and varied clinical needs. You'll assign digital lessons, videos, and assessments...time off with pay. *Please note that although our application mentions a cover letter, we do not require… more
- Merck & Co. (Rahway, NJ)
- …management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions.This position involves… more
- Merck & Co. (North Wales, PA)
- …to help us shape the vision and strategy of our software products in the clinical domain.The Product Manager in this role should be able to define product strategy, ... high value product solutions that improve how we run clinical trials and regulatory submission for our patients, partners,...externally to business and other stakeholders of our IT applications . You will work side by side with Product… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... a detail-oriented and passionate Training Manager to join our Clinical , Medical, Regulatory (CMR) group at Novo Nordisk. This...###. This contact is for accommodation requests only and cannot be used to inquire about the status of applications… more
