- Genmab (NJ)
- …feel like a fit? 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 Tabulation Model (SDTM) standards, perform sponsor oversight...of future strategies and technology-enabled processes and tools for clinical trials standards, change control management and the exchange… more
- Insmed Incorporated (NJ)
- …for patients with serious diseases. In this role, you'll be reporting to the Sr . Manager , Clinical Supply Chain & Logistics.The Insmed Summer Internship ... contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for...scenarios within the fieldAssist supply chain colleagues in the clinical study startup processes such as demand… more
- Parexel (Trenton, NJ)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... **CRA and Sr CRA positions- Remote - Need for SE...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …SummaryThe Study Delivery Lead (SDL) leads the cross functional core and extended clinical study team in end-to end delivery of the clinical trial ... with elements of insourcing. This includes global operational execution and delivery of clinical studies across multiple geographic regions, in adherence to Good… more
- Parexel (Trenton, NJ)
- **Job Purpose:** The Senior Clinical Research Associate I ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) +… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in ... for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international… more
- Parexel (Trenton, NJ)
- …management activities **CSR Narratives (as applicable)** + Performing medical review of Clinical study report narratives according to the client's guidelines and ... and sign off adverse events report for accuracy and clinical importance, relationship to the study drug...processing cycle + Provide input as necessary to Feasibility Studies , Data Monitoring Committees (DMCs), Clinical Endpoint… more
- Parexel (Trenton, NJ)
- …of clinical trial samples + Provides support for sample related matters to clinical study teams + Works with Informed Consent Form (ICF) Specialist and ... Parexel FSP has an exciting opportunity for a Senior Precision Medicine Associate. This role works closely...trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** ** Study … more
- Parexel (Trenton, NJ)
- …assigned project/ study . + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), ... Supporting Activities - Medical Support / Medical Monitoring for projects and studies contracted to Parexel - Deliver all medical support required for successful… more
- Taiho Oncology (Princeton, NJ)
- …to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager , Clinical Research Scientist, you will play a pivotal ... at the forefront of cancer research. Position Summary: The Senior Manager , Clinical Research Scientist...conferences and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr .… more
