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Maintains positive and open communications with physicians, interdisciplinary care team members, Department Head, Lead Clinical Documentation Specialist, coding management and coding staff. Collaborates with coding staff as needed to determine appropriate DRG and required documentation.
$32.64 - $65.01 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform duties related to the hazard identification and control process, safe work planning, inspection and assessment, incident investigation, hazardous materials/waste management, emergency preparedness, fire/life safety, ergonomics, industrial hygiene, training, safe work procedure development, and regulatory compliance recordkeeping and documentation.
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Authors Investigator Brochures (with support from the Medical Writer and other contributors), Clinical Development Plans or similar documents, Core Clinical Trial Protocols, including the CTP strategy and core CTP elements within a document such as Trial Design Synopsis and Paediatric Development Plans, and respective sections of regulatory documentation (CCDS, submission package, and health authority briefing documentation.
$183,000 - $280,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Director, External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process requirement support for the intake, evaluation, documentation, execution and follow-up of External Research (ER) activities, such as Investigator Initiated Studies (IIS) and External Collaborative Research (ECR.
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Applied use of standard electrical engineering analysis and documentation software (i.e. PSPICE, Hyperlynx, Matlab, Mathcad, Orcad, Allegro, and Visio) preferred. Familiarity using DOORS requirements management tool and following a rigorous requirements documentation and validation process desired.
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The TRS is responsible to provide operational expertise to trial teams and Trial Documentation Service (TDS), oversees the implementation of the TMF strategy for the trial and supports the core trial team in all aspects of TMF management, in inspections or audits and in continuous improvement projects.
$32 - $36 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collect and verify site-wide sustainability and circularity data and supporting documentation for external and internal reporting needs to maintain compliance with CSRD and other local, state, and federal reporting requirements.
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Your team, consisting of a secretary, paralegal, support specialist, will assist you in preparing necessary legal documentation, conducting depositions, investigating/researching, and evaluating cases for settlement, arbitration, and trial.
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Day-in-the-Life of a Pharmacy Technician in-Training: Enter prescription information including but not limited to: patient searches, prescriber searches, drug selection, prescription interpretation, insurance billing, and basic documentation.
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Description The Associate Director, External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process requirement support for the intake, evaluation, documentation, execution and follow-up of External Research (ER) activities, such as Investigator Initiated Studies (IIS) and External Collaborative Research (ECR.
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Applied use of standard electrical engineering analysis and documentation software (i.e. PSPICE, Hyperlynx, Matlab, Mathcad, Orcad, Allegro, Visio and CreoView) preferred. Complex analog design including simulation, system/component modeling, signal integrity analysis, component & system level power/stress analysis, servo performance and stability analysis.
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Completes all documentation required by state regulations, and CHC Behavioral Health department by laws in a timely manner, included by not limited to intake, prior authorization request, progress notes, treatment plan documentation, and discharge.
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Conduct site safety assessments and identify all safety hazards on the job site, properly generate and complete JHA, Lock Out Tag Out (LOTO), and other safety-related documentation as per OSHA and site-specific requirements.
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Audits and analyzes loan application, financial statements, credit report, home appraisal, title search, deed, certificate of title, note and other loan servicing documentation to ensure the loan approval decision followed approved policies and procedures, ownership is properly documented, and lien position is secure before proceeding with legal action.
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Transfer data from customer documentation into the DRS NPS designated business systems, which include Deltek Costpoint, Arena Empower, and others. Under direction, prepares contractual documents, including the preparation of contract terms and conditions, and assembles contract documentation packages for submittal.
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author documentation jobs in Ridgefield, CT
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