- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... risk identification and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start-up activities with clinical … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … deliverables across NACD. This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that ... US and CA warehouses operations for US and CA Clinical Trial sites. Accountable for overall performance...projects for NACD & Novo Nordisk (eg Investigators and site staff, vendors etc.). Establish and manage senior level… more
- Bristol Myers Squibb (Trenton, NJ)
- …RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director Clinical Site Operations provides strategic oversight, ... leadership and management of clinical trial execution, including oversight of site management...and other applicable federal (FDA) and state regulations. The Associate Director Clinical Site Operations… more
- Merck (Trenton, NJ)
- …The position will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area, to proactively ... and maintain GCP inspection procedures and guidelines within Global Clinical Trial Operations (GCTO). + Contribute to...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- WuXi AppTec (Cranbury, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Bristol Myers Squibb (Trenton, NJ)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge ... insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on...in their geography + Ensures FM team's execution of clinical trial support activities (as per established… more
- Merck (Trenton, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Merck (Trenton, NJ)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas....seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
- Virtua Health (Marlton, NJ)
- …as required by protocol to ensure the submission of accurate information to clinical trial sponsors and regulatory agencies.* Responsible for submitting all ... Marlton, NJ Additional Locations: Job Information: Summary:Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a… more
- Bristol Myers Squibb (Trenton, NJ)
- …PMP or similar professional certification highly desirable + At least 2 years clinical trial operations experience is required + Comprehensive understanding of ... clinical drug development process + Fluency with Clinical Trial Management System (CTMS) + Strong...out the highest potential of each of our colleagues. **On- site Protocol** BMS has a diverse occupancy structure that… more
- University of Pennsylvania (Philadelphia, PA)
- …the ACC Budget Specialist, Billing Compliance staff, and Finance office to develop clinical trial budgets. Communicating any specialized study budget needs to ... (CRU)- Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work… more
