Clinical Documentation Specialist - Worcester, MA

The chosen candidate will be responsible for maintaining an accurate,cGMP compliant documentation change control system. · ...

This position may have a signing bonus available and is open to applicants with experience in direct patient care, case management or utilization review. The role requires knowledge of clinical documentation practices and principles as well as the ability to interact with physici ...

+The Clinical Analyst supports clinical operations by ensuring accurate and timely management of patient orders, referrals, and clinical results within the electronic health record (EHR).++ Associate or bachelor's degree in health information management, Healthcare Administration ...

This position may have a signing bonus available and is responsible for ensuring accurate medical record documentation to reflect patient severity of illness and risk of mortality. · Works collaboratively with physicians, nurses, and other staff to ensure accurate and complete me ...

++The Clinical Analyst supports clinical operations by ensuring accurate and timely management of patient orders, referrals, and clinical results within the electronic health record (EHR). · Assisting with order closures. · Monitoring referral workflows. · ...

The Clinical Analyst supports clinical operations by ensuring accurate and timely management of patient orders, referrals, and clinical results within the electronic health record (EHR). · ...

The Clinical Analyst supports clinical operations by ensuring accurate and timely management of patient orders and medical results within the electronic health record (EHR). · Assisting with order closures · Maintaining referral workflows · Supporting audits and compliance requi ...

The Clinical Document Specialist collaborates with physicians and other team members to ensure accurate and complete medical record documentation. They review inpatient medical records, analyze clinical status, and communicate with attending physicians to validate observations. · ...

Responsible for supporting ZOLL's Quality System Documentation and the Change Control process (ECOs, ECRs, MCOs, and PDAs) activities related to the ZOLL's Product Lifecycle Management (PLM) System. · ...

We are one of the fastest-growing companies in the U.S. and this may be your opportunity to join us · Storage, retrieval, updating, and reproduction of Engineering, Manufacturing and Quality documentation for the business. · ...

The Quality Control Chemistry Laboratory is seeking a candidate to fill a QC Documentation Specialist III position. · Review assay data for completeness in accordance with SOPs, GDP, and regulatory standards. · Maintain systems for document storage and retrieval. · ...

The Quality Assurance Documentation Specialist I is a quality focused individual who ensures documentation and record keeping processes conform to approved procedures and output documents are accurate. · This role will support the organization by maintaining documents required by ...

The CDI Specialist facilitates and obtains appropriate physician documentation for any patient clinical condition or procedure to support the appropriate severity of illness, · expected risk of mortality,and complexity of care as documented in patient medical records.Completes in ...

The RN Clinical Documentation Specialist facilitates and obtains appropriate physician documentation for any patient clinical condition or procedure to support the appropriate severity of illness, expected risk of mortality, and complexity of care as documented in patient medical ...

The RN Clinical Documentation Specialist facilitates and obtains appropriate physician documentation for any patient clinical condition or procedure to support the appropriate severity of illness, expected risk of mortality, and complexity of care as documented in patient medical ...

This role involves overseeing supplier quality management and generating quality agreements under general supervision. · ...

The Quality Assurance Label Control Specialist at the Devens Cell Therapy manufacturing facility is responsible for supporting site Label Control activities in accordance with Client policies and Global current Good Manufacturing Practices (cGMPs). · Inclusive culture · Focus on ...

Bristol Myers Squibb is seeking a Documentation Specialist to support cell therapy manufacturing operations. · Author and revise Standard Operating Procedures (SOP), and associated documentation for cell therapy manufacturing in accordance with Current Good Manufacturing Practice ...

Bristol Myers Squibb is seeking a Manufacturing Specialist in Technical Documentation for their Cell Therapy Manufacturing team. · This role involves creating and revising Standard Operating Procedures (SOPs) and associated documentation for cell therapy manufacturing in accordan ...

Job summary · This is a manufacturing specialist role in cell therapy manufacturing responsible for creating technical documentation according to current good manufacturing practices. The candidate will collaborate with team members to ensure quality and regulatory compliance. · ...