The Clinical Documentation Specialist facilitates clarification of clinical documentation through concurrent and retrospective interaction with physicians and other members of the health care team to support the capture of appropriate clinical complexity for the level of service rendered to all pati...
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...
Under the direct supervision of the Human Resource Department, this position provides administrative support for the HR staff. ...
Under the direct supervision of the Human Resource Department, this position provides administrative support for the HR staff. ...
Technical WriterDevelop comprehensive documentation that meets organizational standards. ...
Required Licenses/Certifications: Registered Cardiovascular Invasive Specialist. ...
Client is looking for consultant who can join Risk, Compliance & Integrity organization and can brings together critical compliance, assurance, risk and governance functions across and help the company meet compliance needs and enable our businesses to innovate. Assess and advise stakeholders on com...
Responsible for reporting monthly adjustments and corrections to the Compliance Manager. ...
The Compliance Specialist will collaborate with the Compliance Team and Quality/Compliance Manager to develop procedures, policies, and best practices that ensure the company operates within legal and ethical guidelines. Additionally, they will work with the Compliance team to handle customer survey...
This is an opportunity to develop new quality practices that aim to improve quality across our Open World titles. Lead Quality Analyst - Open World Specialist. EA is looking for a Lead Quality Analyst to join one of our teams testing Open World experiences. You will have the end-to-end ownership of ...
The individual will also assist in quality operations area, such as batch record and quality control data review, line clearances, AQL inspection, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs. Quality Assurance Specialist II. The ...
USDS Financial Crime Compliance is responsible for overseeing and operationalizing all aspects related to Anti-Money Laundering (AML) and Sanctions Compliance activities related to TikTok USDS's operations. As a Financial Crimes Compliance Specialist, you will be responsible for risk mitigation acro...
Vaxcyte is looking for a talented Document Specialist, who will be responsible for managing manufacturing documents in a GXP compliant environment. Perform document specialist functions in QA, including managing the lifecycle of GMP documents in Veeva, including creation, revision, approval, distrib...
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Develops and conducts specialized education and public information classes in their area of specialty; responsible for the clinical investigation of assigned new drugs in the specialty. Consults on pharmacokinetic and pharmacogenomics and potential effects concerning the use of new drugs, those in i...
Ensures the correct and timely implementation of document requests in editing of controlled documentation. Document storage and retrieval may require lifting boxes of documents, carrying documents from one place to another and storing boxes on shelves or in file cabinets. Processes document workflow...
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. Neonatal Clinical Nur...
This unique position requires strong administrative abilities, outstanding customer service, and proficiencies in logistics. ...
As a Global Patient Safety (GPS) Trial Master File (TMF) Specialist, you will be the GPS TMF lead in the cross-functional management of TMF for Company’s clinical studies. Serve as the GPS TMF lead in the cross-functional management of TMFs for all clinical studies. Adhere to applicable Standard Ope...
Vaxcyte is looking for a talented Document Specialist, who will be responsible for managing manufacturing documents in a GXP compliant environment. Perform document specialist functions in QA, including managing the lifecycle of GMP documents in Veeva, including creation, revision, approval, distrib...
Quality Assurance Specialist / Customer Support (US). Review design plans, process procedures, test procedures, and quality manuals to understand the problem's scope, requirements, and function. Ensure that products meet the organization's and customers' quality and product integrity requirements. A...
This is an excellent opportunity for a person that has strong experience in audit best practices and previous experience in designing and adhering to processes for R&D compliance. Consult closely with senior leadership within the QIAGEN Digital Insights organization to evaluate and prioritize re...
Mytra's Systems Engineering team is looking for a Technical Writer Lead to build and own our technical documentation infrastructure. As Technical Writer Lead, you will work across disciplines to distill interdisciplinary information for system-level components into documentation for internal and ext...
An accountable team player who is detail and quality oriented with solid understanding of quality assurance principles, systems, and procedures. Interact with contract manufacturers to resolve quality issues with minimal supervision. Participates in developing Standard Operating Procedures (SOPs) to...
The Document Control Specialist or ECO Analyst is responsible for overseeing and maintaining accuracy within the change management system. ...