- Taiho Oncology (Princeton, NJ)
- …and Abilities: + 7-10 years combined experience in academic and/or industry oncology clinical research and drug development, including experience as medical ... (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents,... studies . + Review and sign off on clinical documents related to clinical studies… more
- Merck (Rahway, NJ)
- …MD or MD/Ph.D. with a minimum of 10 years' experience in oncology biomarker studies and translational clinical research **Required Experience and Skills:** + ... Biomarker Development, Biomarker Research , Clinical Development, Clinical Research , Diagnostics Development, Drug Development, Immuno-Oncology,… more
- Parexel (Trenton, NJ)
- …a sound business strategy. **Knowledge and Experience** : + Demonstrated understanding of clinical research , the drug development process, and industry ... Writer will research , create, and edit all documents associated with clinical research . Responsibilities also include: acting as primary client contact for… more
- Atlantic Health System (Morristown, NJ)
- …files. Documents subject progress according to good clinical practices in research records. Maintains study drug /device accountability records as ... per regulatory requirements, sponsor requirements and policies and procedures. + Writes study drug prescriptions for trial subjects in accordance with applicable… more
- Parexel (Trenton, NJ)
- …compliance and audit requirements in a GxP environment. + Demonstrated understanding of clinical research , the drug development process, and industry ... we are dedicated to improving patient lives through innovative clinical research and regulatory solutions. As a...ICH-GCP. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study … more
- Parexel (Trenton, NJ)
- …a sound business strategy. **Knowledge and Experience** : + Demonstrated understanding of clinical research , the drug development process, and applicable ... Medical Writer will research , create, and edit all documents associated with clinical research . The Senior Medical Writer may operate as the project lead… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …changes for internal and external studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and ... role applies to internally sourced studies and studies out-sourced to Clinical Research ...of vendor contracts, budget, TMF, and study drug accountability + Contributes to clinical … more
- Regeneron Pharmaceuticals (Warren, NJ)
- … trial delivery. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance ... sites may be required to assist with monitoring clinical studies . **A typical day in this... study + Oversees and provides input to study drug and clinical supplies… more
- Taiho Oncology (Princeton, NJ)
- …Plan. The Senior Study Manager (SSM) is responsible for ensuring assigned clinical studies are delivered within timelines, budget, and quality. A critical ... establish and monitor trial milestones as well as overall day-to-day operations of clinical studies , ensuring study information and timelines are accurate… more
- Vitalief (Newark, NJ)
- …to $50,000 (commensurate with experience). RESPONSIBILITIES: + Under the direction of the Clinical Research Study Site Leader, support the planning, ... concurrent Medical Oncology interventional studies (Phase II-III). Studies are largely drug and biologic trials...surgical components. + Independently manage day-to-day clinical research activities across the full study lifecycle,… more