- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist -Engineering position will report to the Associate Director, Engineering and ... interfacing with scientists who are manufacturing drug substance to support early clinical studies, scaling up new chemistries, and exploring new technologies. -… more
- Merck & Co. (Rahway, NJ)
- …At our company, we're shaping the future of health. We're seeking a Clinical Database Developer who will be instrumental in creating and developing clinical ... Core Responsibilities Your primary role will be to create and develop clinical databases and data transfer files, ensuring they align with written specifications.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials ... for the quality review of the URS and UAT deliverablesDevelop UAT documentation consisting of: test plans and scripts, pre, post, specification reviewer and… more
- Merck & Co. (Rahway, NJ)
- …or other tools.Organize, store, archive, and retrieve contracts, payment documentation and other relevant documents.Coordinate records management practices and ... Skills & Experience Education:High School Diploma and minimum of 7 years of clinical payment experience.Associates or Bachelor's Degree and minimum of 3 years of … 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... tools, SOPs, NNI-GS Agreements, FDA safety reporting guidelines and Good Clinical Practice (GCP) to ensure adherence/compliance Plan, oversee, coordinate , conduct… 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)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Warehouse Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Warehouse 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)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role ... OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP… 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New ... be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift. This… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... Quality Assurance Document Control Specialist role is an exempt position responsible for supporting...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QC Microbiology Specialist , Lentivirus CAR-T Manufacturing as part of the Quality team based in ... The current openings are on the third shift.Role OverviewThe QC Microbiology Specialist , Lentivirus Vector (LVV) CAR-T Manufacturing is an exempt level position with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Technical Equipment Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/systems required to...of the CAR-T Equipment team in support of on-going clinical and commercial manufacturing as well as facility expansions… more
- Penn Medicine (Plainsboro, NJ)
- …Our employees shape our future each day. Are you living your life's work? **HIM Clinical Documentation Specialist ** Job Summary: + The Clinical ... the clinical care teams and the Corporate HIM teams, the Clinical Documentation Specialist will educate and utilize compliant questions and tools toward… 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
- WMCHealth (Valhalla, NY)
- Clinical Documentation Specialist Company: NorthEast Provider Solutions Inc. City/State: Valhalla, NY Category: Professional/Non- Clinical Department: ... CDIP: Clinical Documentation Improvement Practitioner . CCDS: Certified Clinical Documentation Specialist . CCS: Certified Coding Specialist , or… more
- BronxCare Health System (Bronx, NY)
- Overview The Clinical Documentation Specialist will work with Senior Director in physician education regarding documentation that meets severity of ... Responsibilities + Provides concurrent and retrospective review of the clinical documentation in the medical record; review...Hospital Center - Concourse Max USD $94,000.00/Yr. Shift Varies Department : Name Clinical Doc Specialist Depart… more
- Catholic Health Services (Rockville Centre, NY)
- Overview Clinical Documentation Specialist Rockville Centre, NY Explore a career with Mercy Hospital, a 375-bed not-for-profit hospital and member of ... require additional physician input. Facilitates and secures clarification of accurate clinical documentation to ensure that appropriate reimbursement is received… 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
