Clinical Documentation Specialists are responsible and accountable for the day-to-day management and success of the Continuous Documentation Improvement Project to include all modalities, acting as a liaison with specific department staff, speaking, meeting and educating physicians, residents and mi...
Build out documentation (website). Developing process flow documentation and -pager docs providing guidance as it pertains to Search Platforms. Develop, monitor and update website documentation as needed. ...
As a Clinical Documentation Improvement Specialist, you will be responsible for improving the overall quality and completeness of clinical documentation by expediting clarification to clinical documentation. Clinical Documentation Improvement Specialist. We are seeking an experienced and detail-orie...
Responsible for reporting monthly adjustments and corrections to the Compliance Manager. ...
The Lead Technical Writer is responsible for creating, updating and maintaining Cilium documentation as a whole, the main part of it being developer and user documentation. You will be at the forefront of our users' experience for both Cilium OSS and Cilium Enterprise, making the most technically ad...
The QA Specialist III / IV will provide QA support for Quality Operations. Support the analysis and reporting of product and process quality trends, and quality system performance against internal and external guidelines, standards, and regulations. Extensive experience with Quality Assurance syste...
Performs all required applications specialist responsibilities including but not limited to: creating and maintaining formal customer training support documents; design and oversee the initial and ongoing training for Clinical Applications Specialists, as well as, continued training for new product ...
The technical writer will create and update the technical documentation associated with the following:. ...
Reporting to the Sr Manager of Global Quality Assurance for Raw Materials and Reagents Center of Excellence, you will assist with managing the activities of the Quality Assurance department and supervise quality assurance efforts to ensure conformance to Company Pharmaceutical quality standards and ...
Create a schedule for clinical staff to ensure adequate clinical support during hours of business operations. Clinical Service Supervisor role. The successful Clinical Service Supervisor candidate will be someone who has demonstrated the ability to be a self-starter and successful problem solver wit...
The Quality Assurance Specialist I plays a critical role in ensuring the quality and compliance of products and processes within the organization. This role is responsible for monitoring and evaluating quality assurance standards, conducting audits, identifying areas for improvement, and implementin...
Quality Assurance Operations Specialist II. An accountable team player who is detail and quality oriented with solid understanding of quality assurance principles, systems, and procedures. Demonstrates working knowledge of quality assurance systems, methods and procedures. Interact with contract man...
Ready to jump into the fast lane? Our client, a game-changing private equity firm in Redwood City, CA, needs a powerhouse Executive Assistant to be the right hand to their bold and visionary CEO. As the Executive Assistant, you'll be the orchestrator of the CEO’s fast-paced world, ensuring everythin...
Technical proficiencies and performance are at the experienced level of all Clinical Specialists in the region. Demonstrated advanced knowledge of cardiac pacing systems is also necessaryMust apply engineering skills and abilities to interpret and solve complex clinical problemsMust have comprehensi...
Compliance, Audit, Regulatory, NCR, ISO, Data entry, Quality assurance, Regulatory compliance, Gmp. In compliance with FDA, European MDD/MDR & ISO regulations, the Sr. Specialist will perform work under general supervision. Assist in managing compliance to the current revisions of the standards. ...
The Clinical Research Coordinator will be responsible for multiple administrative tasks related to the organization of multiple internal and external clinical Client sponsored trials including IRB submissions, along with upkeep of clinical documentation as necessary. Assist the field Clinical Develo...
Clinical Practice Quality Specialist - Hematology / Oncology / Stem Cell Transplant. Clinical Practice Quality Specialists are Registered Nurses with advanced degrees who utilize evidence-informed practice to facilitate and lead improvements in patient care and in the work environment. The Clinical ...
Clinical Nurse Specialists assess, plan, provide and evaluate specialized nursing care of patients by advancing the quality and scope of nursing practice through clinical practice, education, research, consultation, and administrative roles in the area of clinical expertise (e. Clinical Nurse Specia...
Manager / Senior Manager, Compliance & Reporting Specialist. Work with KPMG's extensive network of specialists & enjoy access to our Ignition Centers, where deep industry knowledge merges with cutting-edge technologies to create innovative tax solutions. KPMG is currently seeking a Manager / Senior ...
Attention to detail is paramount in technical writing, particularly in maintaining consistency in formatting, style, and adherence to brand guidelines. Be adept at troubleshooting and problem-solving, especially when faced with challenging technical concepts or ambiguities in requirements. ...
Under moderate supervision, the individual will be working in the Quality Systems team for providing quality oversight of the lifecycle management of GxP Facilities, Utilities, Equipment, Analytical Instruments, and Computerized Systems. Perform a wide variety of quality assurance activities to ensu...
Document Imaging specialist is also responsible work using automated workflows for point of care scanning This position is responsible for providing basic, routine maintenance of the scanning equipment The DI Specialist resolves problems with documents such as missing Medical Record Numbers, account...
Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports).Review/approval of...
You will primarily be responsible for: development, execution, evaluation and ongoing supervision of individual and project action plans in order to improve patient care outcomes; create policies and procedures; conduct independent assessment of patients and their current treatment plans; collaborat...
As the Document Control Specialist, you will be responsible for developing and maintaining document transmittals, records, and systems for our client's first commercial scale projects. Perform project document control activities such as ECN (Engineering Change Notice), managing the distribution matr...