Clinical Documentation Specialist 3 - Bend, OR

This is a QA Documentation Specialist I position that involves continuous development and knowledge of GMP regulations. · ...

Support implementation and continuous improvement of Quality Systems. · ...

This role involves continuous development and knowledge of GMP regulations. · Control record management including receipt, reconciliation, scanning and verification. · ...

Continuous development and knowledge of GMP regulations. · ...

This role involves continuous development and knowledge of GMP regulations. · ...

The role ensures accurate control of records and documentation, supports audit activities, and provides guidance on GMP practices while maintaining high standards of compliance and data integrity. · ...

Maintain and continuously develop knowledge of GMP regulations. · Support the implementation and ongoing improvement of Quality Systems. · ...

We are seeking a QA Documentation Specialist I to join our team at ASK Consulting. · Continuous development and knowledge of GMP regulations · Support implementation and continuous improvement of Quality Systems · ...

The Clinical Documentation Specialist reviews and analyzes patient documentation to support accurate capture of complexity and severity of illness. Utilizes queries with medical staff for completeness. · Maintains current knowledge on Medicare's rules, conducts reviews for system ...

Maintain and continuously develop knowledge of GMP regulations. · Maintain and continuously develop knowledge of GMP regulations. · Support the implementation and ongoing improvement of Quality Systems. · ...

Continuous development and knowledge of GMP regulations. Support implementation and continuous improvement of Quality Systems. · Control record management including receipt, reconciliation, scanning and verification, record check-out/check-in and maintain scanned record back-ups ...

Dice es la plataforma líder para expertos del sector tecnológico a cada etapa de sus carreras. · Desarrollo continuo y conocimiento de las regulaciones GMP · ...

Continuous development and knowledge of GMP regulations. Support implementation and continuous improvement of Quality Systems. · ...

Continuous development and knowledge of GMP regulations. Support implementation and continuous improvement of Quality Systems. · Controlled document and record review. · Batc Record issuance. · Create and issue logbooks. · ...

· This Clinical Documentation Specialist 3 will review medical records for accuracy and completeness of patient visits. They will collaborate with physicians, mid-level providers, ancillary staff, and medical records coders. · ...

+Job summary · The Case Management Liaison supports the Case Management team to assist with the completion of required forms/documentation, coordination of care, and post-acute follow-up arrangements. · +ResponsibilitiesSupports discharge planning activities under the direction o ...

The Fixed Assets Specialist II plays a foundational role in supporting the organization's asset accounting operations by ensuring that fixed asset records are accurately maintained in accordance with company policy and accounting standards.This role offers a strong entry point in ...

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Be part of our mission to transform healthcare, improve lives and drive meaningful change with Noctrix Health. · Travel to patients homes or mutually agre ...

We're hiring a Quality Inspector / Compliance Specialist to help ensure that standard products perform flawlessly when it counts.This role is ideal for hands-on aerospace inspectors who also values documentation and traceability in regulated environments. · ...

The Medical Laboratory Scientist at St. Charles Health System performs, interprets and reports clinical laboratory testing on a variety of human biological specimen types. ...