- Community Health Systems (Fort Wayne, IN)
- … Specialist or ICD-10 certification or trainer designation required or Certified Clinical Documentation Specialist (CCDS) required RHIA - Registered ... Job Summary The Clinical Documentation Improvement (CDI) Specialist Lead provides advanced support for CDI activities within the facility, ensuring the… more
- Elevance Health (Washington, DC)
- …Health Information Technician (RHIT), Registered Health Information Administrator (RHIA), Certified Clinical Documentation Specialist (CCDS), Certified ... Validation Auditor-RN is responsible for auditing inpatient medical records to ensure clinical documentation supports the conditions and DRGs billed and… more
- Christus Health (Wake Village, TX)
- …home, etc. Verify patient allergy information and ensure complete documentation (ie, substance, allergy category, reaction description). Utilizes available resources ... process with the pharmacist. SECONDARY JOB FUNCTIONS Use good clinical judgment skills to determine the accuracy of medication...Department setting Ability to log on to an electronic clinical data base to determine if a medication list… more
- Banner Health (Phoenix, AZ)
- …knowledge through education, research, and innovation. As an Emergency Department Clinical Pharmacy Specialist at Banner University Medical Center Phoenix ... you will be responsible for developing and maintaining a high-level clinical pharmacy practice in Emergency Medicine. Patient care responsibilities include ensuring… more
- Community Health Systems (Franklin, TN)
- Job Summary The Clinical Utilization Review Specialist is responsible for evaluating the necessity, appropriateness, and efficiency of hospital services to ... collaborates with healthcare providers to facilitate efficient patient care. The Clinical Utilization Review Specialist monitors adherence to hospital… more
- GE HealthCare (Lansing, MI)
- Job Description Summary The Clinical Application Specialist (CAS) will deliver clinical and operational expertise by providing excellent education and ... training support within a specific modality (CT) or product portfolio to clinical end-users. These clinical experts will facilitate evidence-based practice and… more
- GE HealthCare (Sacramento, CA)
- …makes a difference, and every difference builds a healthier world. As a Clinical Applications Specialist (CAS) supporting the GE Healthcare imaging applications ... team you will deliver clinical , technical and operational expertise by providing excellent adult education and training supporting the PET modality. As a clinical… more
- GE HealthCare (Boston, MA)
- Job Description Summary The Clinical Applications Specialist (CAS) delivers Life Care Solutions (LCS) clinical and operational expertise by providing ... education and training support for the monitoring product portfolio to clinical end-users. These clinical experts will facilitate evidence-based practice… more
- Edwards Lifesciences (Kansas City, KS)
- …you'll make an impact: Field monitoring of studies and data collection for clinical trials, assess all data documentation , reports, records, transcripts, exam ... results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as… more
- Bristol Myers Squibb (Devens, MA)
- …with our Cell Therapy team. BMS Cell Therapy Manufacturing is seeking a Specialist , Lead Clinical Manufacturing Associate, Cell Therapy that bring enthusiasm, ... manufacturing operations for Cell Therapy. This role is key to start up of Clinical Trials at Devens in a multi-product Cell Therapy Facility. Shifts Available: TBD… more
- Stanford Health Care (Newark, CA)
- …- 08 Hour (United States of America) Job Description The Patient Administrative Specialist is a flexibly staffed career ladder consists of five levels. Individuals ... job tasks. Meet/Exceed organizational and department service standards. Answers non- clinical CRMs, escalating where appropriate. Answers non- clinical patient… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III 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)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Specialist , QA Process Excellence as part of the Quality team based in Raritan, ... NJ.Role OverviewThe QA Process Excellence Specialist III role is an exempt level position with...within a cell therapy manufacturing plant 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 Document Control Specialist as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Document Control Specialist role is an exempt level position with responsibilities...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 QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Validation Specialist role is an exempt level position with responsibilities...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- ALPCO (CA)
- …Applications Specialist will serve as a trusted advisor to clinical , academic, and pharmaceutical customers, functioning as both a technical problem-solver and ... research and medical diagnostic industries. Customer segments include routine clinical laboratories, biotech and pharmaceutical R&D groups, CROs, and academic… more
- Merck & Co. (Rahway, NJ)
- …to create a frictionless flow of data from source systems to regulatory documentation .- - - Under the guidance of dCMC Regulatory Authoring Leadership, the Senior ... Specialist , Regulatory Authoring Business Analyst,-will optimize regulatory authoring processes...capabilities to ensure effective digital solution integration and adoption. Documentation and Project Management Support: The analyst will create… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with...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 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)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner… more
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