- Merck & Co. (Rahway, NJ)
- …& Disclosure Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in ... documents for clinical studies in all therapeutic areas. - The Specialist will be responsible for: Authoring scientifically valid clinical trial registration… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... OverviewThe Operations Support Specialist will be part of the Technical Operations team...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist I as part of the Technical Operations team based in Raritan, NJ. ... for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Inventory Control Specialist as part of the Technical Operations team based in Raritan, New ... Jersey. Role OverviewThe Operations Inventory Control Specialist will be part of the Raritan CAR-T Operations team responsible for building operations activity area… more
- Hackensack Meridian Health (Edison, NJ)
- **Overview** The ** Clinical Documentation Specialist RN** facilitates improvement in the overall quality, completeness and accuracy of medical record ... to the unit. **Responsibilities** A day in the life of a ** Clinical Documentation Specialist RN** at Hackensack Meridian Health includes: + Facilitates… more
- Mount Sinai Health System (New York, NY)
- **Job Description** MSHP seeks a Clinical Documentation Specialist who will support efforts to improve the overall quality and completeness of clinical ... or more of the following, required: o Certified Coding Specialist (CCS) o Certified Risk Adjustment Coder (CRC) o...and past medical history to identify potential gaps in clinical documentation related to outpatient encounters, with… more
- Mount Sinai Health System (New York, NY)
- **Job Description** MSHP seeks a Clinical Documentation Specialist who will support efforts to improve the overall quality and completeness of clinical ... or more of the following, required: + Certified Coding Specialist (CCS) + Certified Risk Adjustment Coder (CRC) +...and past medical history to identify potential gaps in clinical documentation related to outpatient encounters, with… more
- RWJBarnabas Health (Livingston, NJ)
- …/ 7:30a 3:30p / 8a-4p + 37.5 hrs weekly Essential Functions: The Clinical Documentation Specialist (CDS) responsibilities include assisting in clarifying ... Clinical Document Specialist , Clinical Documentation ManagementReq #:0000148777 Category:Nursing Status:Full-Time Shift:Day Facility:Cooperman Barnabas… more
- Hackensack Meridian Health (Hackensack, NJ)
- …(CDMP) chart reviews for accuracy and compliance when there is a discrepancy in the Clinical Documentation Specialist and Coder DRG and coaching of the CDMP ... missing, conflicting, documentation . + Extensively reviews all physician and clinical documentation , lab results, diagnostic information and treatment plans… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The FPA Facility Fee Coding Specialist reviews clinical documentation and diagnostic results to extract data and apply appropriate ICD-10 ... surgical and non-surgical procedures for facility services rendered. Assesses support documentation . + Provides written reports to supervisor or manager with audit… more
- Abbott (New York, NY)
- …of care. **What You'll Work On** The job purpose and scope of the Structural Heart Clinical Lead Specialist (CLS) is an integrated part of clinical trials ... the training & sales department to be an extension for field preceptorship initiatives. The Clinical Lead Specialist is to support Abbott TAVI US clinical … more
- Bristol Myers Squibb (New Brunswick, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . Our Clinical Supply Operations is responsible for the supply of drug product ... administered to patients in clinical studies worldwide. In Global Product Development and Supply...preconditioned as necessary. + Prepare accurate transportation and customs documentation by collecti ng and compiling relevant shipment details… more
- Abbott (New York, NY)
- …enable outcomes that advance the standard of care. The job purpose and scope of the Clinical Sales Specialist (CSS) role is to provide TAVI clinical trial ... accounts within a defined region. In this role, the Clinical Sales Specialist will be an integrated...inventory & acquisition and field trunk stock + Provide documentation as required for quality assurance initiatives + Co-develop… more
- Medtronic (New York, NY)
- …more connected, compassionate world. **A Day in the Life** At Medtronic, the Clinical Specialist , supports the Neuromodulation Pain and Target Drug Delivery ... of normal business hours and at the discretion of Clinical Specialist Manager * Adheres to company...company policies and complies with required event reporting and documentation , utilizing Medtronic technology tools * Responsible for managing… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …and become your best self. Become a **maker of possible** with us. The **Sr. Clinical Quality Specialist ** is responsible for supporting the Global Clinical ... integrity are maintained while also encouraging innovative research solutions. Partners with clinical study teams in a way that fosters open and trusting dialogues.… more
- VNS Health (Manhattan, NY)
- …benchmarks for patient outcomes, satisfaction cost and regulatory requirement. + Conducts clinical reviews with primary care providers or specialist to address ... interdepartmental quality improvement activities such as development and engagement, clinical review, clinical risk management, and patient satisfaction.… more
- Merck (Rahway, NJ)
- …(Bulk Drug Product and Clinical Finished Goods). + Responsible for authoring clinical supply documentation in support of labeling and packaging activities as ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...well as supply chain documentation to support critical CMC activities. + Responsible for… more
- Abbott (New York, NY)
- …department in education/training of new employees in the region (sales reps, clinical specialists, field clinical engineers, etc.). + Provides sales support ... during or following cases such as completing the necessary documentation (for example: implant registration, temporary id cards, packing list) and is able to execute… more
- VNS Health (Manhattan, NY)
- …case reviews requested by enrollees, including preparing and submitting documentation according to regulatory requirements and tracking external reviews throughout ... the process. External reviewers include New York State (Fair Hearings), Centers for Medicare and Medicaid Services (CMS), Independent Review Entities and Quality Improvement Organizations. + Collaborates with professionals, health plan departments such as… more
- The Center for Great Expectations (East Orange, NJ)
- …recovery meetings. + Participate in planning and delivery of social support and clinical groups. GENERAL DUTIES: + Provide timely documentation for all ... Peer Recovery Specialist , START Program East Orange, NJ (http://maps.google.com/maps?q=7+Glenwood+Avenue+East+Orange+NJ+USA+07017) Job Type Full-time Description… more
