The Clinical Documentation Improvement Specialist (CDS) is responsible for reviewing the medical record for technical accuracy, specificity, and completeness of provider clinical documentation. The CDS is responsible for initiating and completing the query process to ensure complete documentation. C...
Reporting to the Senior Director, Quality Engineering, the Quality Specialist is responsible for managing and supporting the creation, maintenance, and closure of Device Quality Management System (QMS) records. The Quality Specialist will perform tasks that will uphold and improve the product qualit...
Job Title: Specialist - Documentation (Mid Level). Bachelor's degree and 3-5 years experience or equivalent The Documentation Coordinator I is responsible for the control of Quality Management System (QMS) and quality specific GMP critical documentation. Develops, produces, and maintains a variety o...
The loan processor performs a variety of activities to support the underwriters and ensures loans are processed and closed within departmental policy and compliance regulations. Reviews and issues the Loan Estimate and initial application package using the loan origination system; verifies all infor...
...
May train/coordinate work for new administrative assistants. Responsible for all administrative functions of the Quality Assurance department: answering phones, calendar management, scheduling travel, managing correspondence and scheduling couriers, processing expense reports, meeting/event planning...
About the job Remote Clinical Business Operations Specialist. Remote Clinical Business Operations Specialist needs systems savvy resource with good communication skills. Remote Clinical Business Operations Specialist requires:. Clinical Operations, Project Management, Clinical Outsourcing, and/or CR...
The successful candidate will work with the existing Division Administrative Assistant on a wide variety of administrative support tasks, and co-lead the Group Administrative Assistant team to promote best practices and triage any issues that may arise. The Engineering Division is seeking an Adminis...
Respond to internal requests for regulatory and clinical research input, and clinical documentation to support commercial license/approval submissions, publications and technical presentations, and collaborate with clinical and other departments regarding global clinical regulatory requirements (EU ...
Execute duties associated with controlled documents; review, edit, format master documents according to approved procedures and templates, maintains document properties (metadata), monitor document status and approval notifications, distributions, and archiving. Implement, maintain, and continuously...
The Technical Writer will create, test and maintain the structured content templates and deployment materials leveraging Amazon and industry standards for effective information sharing. The technical writer will also be required to work effectively with customers and internal partners to understand ...
The Security Compliance Specialist is responsible for managing security compliance for BCG's software and data offerings in alignment with industry standards. The Security Compliance Specialist will work closely with product and engineering, security, and IT teams. The ideal candidate must have a st...
The Document Imaging Specialist ensures health record documents are accurately entered into the patient electronic health record in a timely basis. We are currently hiring a Document Imaging Specialist based in Worcester. Including scanning and filing paper documents and uploading and filing electro...
The loan processor performs a variety of activities to support the underwriters and ensures loans are processed and closed within departmental policy and compliance regulations. Reviews and issues the Loan Estimate and initial application package using the loan origination system; verifies all infor...
Communicate and share project and technical information willingly across project teams and within the Waters technical writing community. Technical Writer, DITA, HTML, XML, science, instrument, hardware, engineer, chemistry, laboratory, publishing, content development, user documentation, AI, editin...
We are currently looking for PRN Medical Office Administrative Assistant to work as needed at our Occupational Health and Wellness center located in Andover, MA. In this role you will provide PTO coverage for 3-5 fulltime Assistants as needed. This position provides administrative support with the d...
Clinical Specialist**Requisition Number **2769**Location **US - Marlborough, MA**State/Territory **Massachusetts****Company Overview:**Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio and a global distribution footprint. Keep up to date with the...
The Clinical Training Specialist will be a subject matter expert on Boston Scientific's Electrophysiology product portfolio, including but not limited to the VersaCross RF Transseptal Solution and FARAPULSE Pulsed Field Ablation System. The Clinical Training Specialist will partner with professional...
We currently have a great opportunity for a Clinical Applications Specialist I. The Clinical Applications Specialist (CAS) is part of a multidisciplinary team that supports the equipment and middleware integration process from order to go-live in the laboratory environment. Our agile, resourceful te...
The Principal Clinical Quality Assurance Specialist assists with internal quality assurance program for the assigned business area. Serves as clinical QA representative on clinical project teams and conducts internal and external quality audits to assure that BSC clinical trials comply with all appl...
The Lead Compliance Specialist will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The successful candidate will foster compliance across a broad range of Quality Assurance areas and will work closely with ta...
Oversee multiple projects concurrently, ensuring that quality standards are consistently achieved. Analyze and review test packets, creating detailed test logs to track quality assurance. Address quality issues promptly and develop effective solutions. Create or update procedures for capturing, inve...
Actively participates in continuous improvement opportunities to identify efficiencies and compliance improvements to benefit department operations or the organization at large. Authors (or assists in authoring) new or revised standard operating procedures (SOPs) for the QA department to satisfy new...
Executive Administrative Assistant. Orion Group is seeking an Executive Administrative Assistant to work onsite for our pharmaceutical client in Worcester, MA. Minimum 3 years of administrative assistant related experience. Responsibilities include all administrative functions of the department: ans...
Compliance Specialist – Rate Filing. Be sure to include your preferred contact information as one of our Qualification Specialists will connect with you promptly. ...