- 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's ... Research Laboratories portfolio of clinical trials. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to … 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 of our ... Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical … more
- Merck & Co. (Rahway, NJ)
- …technical solutions with the highest value, that improves the way we run our clinical trials for our patients, our partners, and our employees.Candidate will have a ... and innovation to:Invest in data that fuel innovationModernize our current state clinical technology and business processes by implementing a new unified clinical… more
- RWJBarnabas Health (Oceanport, NJ)
- Clinical Document Specialist ( Hybrid )Req #:0000175115 Category:Clerical / Administrative Support Status:Full-Time Shift:Day Facility:RWJBarnabas Health ... 2 Crescent Place, Oceanport, NJ 07757 Job Overview: A clinical documentation specialist (CDS) reviews a patient...Jersey Licensed Registered Nurse Scheduling Requirements: + Working Hours: Hybrid - four days onsite, one day remote +… more
- Merck (Rahway, NJ)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our ... Company's Research Laboratories portfolio of clinical trials. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical … more
- Merck (Rahway, NJ)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... of our Research & Development Division portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical … more
- Merck (Rahway, NJ)
- …technical solutions with the highest value, that improves the way we run our clinical trials for our patients, our partners, and our employees. Candidate will have a ... to: + Invest in data that fuel innovation + Modernize our current state clinical technology and business processes by implementing a new unified clinical … more
- Bristol Myers Squibb (New Brunswick, NJ)
- …the Quality Narrative at the study and/or ASSET and TA levels to document end-to-end RBQM for critical to quality (CtQ) data, processes, and vendors, demonstrating ... and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a...at a study and/or ASSET and TA level, to document the end-to-end risk-based quality management for CtQ data,… more
- Weill Cornell Medical College (New York, NY)
- Title: Web Operations and Support Specialist Location: Midtown Org Unit: Web Operations Work Days: Weekly Hours: 35.00 Exemption Status: Exempt Salary Range: ... Hired for NYC Offices **Position Summary** The Web Operations and Support Specialist is responsible for managing daily operations and providing technical support for… more
- Bristol Myers Squibb (Summit, NJ)
- …the ability to help patients are incredible. **The Position:** The Operations Specialist , Scheduling and Cell Logistics will be responsible for monitoring patient ... treatment schedules for the manufacturing of BMS's clinical and commercial autologous cellular immunotherapy products. They will resolve real-time operational issues… more
- Amgen (New York, NY)
- …and transform the lives of patients while transforming your career. **Field Reimbursement Specialist Senior Manager - East** **What you will do** Let's do this. ... through field visits and virtual meetings + Develop and document workflows and procedures and ensure FRS are informed...arena or pharmaceutical industry in sales, managed care, or clinical support OR Master's degree AND 4 years of… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …the Quality Narrative at the study and/or ASSET and TA levels to document end-to-end RBQM for critical to quality (CtQ) data, processes, and vendors, demonstrating ... and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a...at a study and/or ASSET and TA level, to document the end-to-end risk-based quality management for CtQ data,… more
- Deloitte (New York, NY)
- …in a collaborative environment? As an experienced Epic Pharmacy & Willow Project Delivery Specialist you will have the ability to share new ideas and collaborate on ... complex changes and test builds/enhancements, new releases etc. and document all outcomes of testing and serve as the...by harnessing deep sector knowledge, scaling the power of hybrid services and products, and unlocking the power of… more
- NYU Rory Meyers College of Nursing (New York, NY)
- …determine resolutions, and provide solutions; report on findings; recommend and document solutions. Assess, initiate, plan, and manage incident tracking database ... base pay only and excludes any additional items such as incentives, bonuses, clinical compensation, or other items. NYU aims to be among the greenest urban… more
- Robert Half Legal (New York, NY)
- Description Robert Half is seeking a Procurement Specialist with experience in managing outsourced services related to our company's clinical trials and ... to the development pipeline. This role requires an individual with proven clinical trial outsourcing experience and a strong understanding of the drug development… more
