Job Closed

This listing is no longer active.

Memorial Hermann Health System logo
Memorial Hermann Health System

More than a century of patient-centered care. At Memorial Hermann, we are all about advancing health.

Clinical Documentation Specialist

Medical writerMedical writerFull TimeRemoteSeniorTeam 10,001+H1B SponsorCompany SiteLinkedIn

Location

Texas

Posted

5 days ago

Salary

0

Seniority

Senior

Bachelor Degree5 yrs expEnglish

Job Description

Clinical Documentation Specialist

Memorial Hermann Health System

• This position is responsible for concurrent review of inpatient medical records in order to identify opportunities for improving the quality of physician documentation • Facilitates modifications to clinical documentation through concurrent interaction with physicians (face-to-face and electronically) and other members of the health care team • The goal of this position is to achieve a complete medical record in order to support complete, accurate and timely coding • Communicates with physicians, case managers, coders, and other healthcare team members to facilitate comprehensive medical record documentation to reflect clinical treatment, decisions, and diagnoses for inpatients • Utilizes the hospital’s designated clinical documentation system to identify opportunities for physician and hospital outcomes • Provides or coordinates education to all internal customers related to compliance, coding, and clinical documentation issues and acts as a consultant to coders when additional information or documentation is needed to assign the correct DRG • Responsible for the day-to-day evaluation of documentation by the medical staff and healthcare team in accordance with the hospital’s designated clinical documentation system • Gathers and analyzes information pertinent to documentation findings and outcomes • Contributes to a positive working environment and performs other duties as assigned or directed to enhance the overall efforts of the organization • Develops physician education strategies to promote complete and accurate clinical documentation and correct negative trends • Identifies patterns, trends variances and opportunities to improve documentation review and process • Researches literature and stays abreast of CMS rules and regulations, incorporating changes to daily practice for overall documentation enhancement • Assists in the development and reporting of performance measures to the medical staff and other departments and prepares physician specific data information • Conferences with key physicians to review outcome information (including physician profile data if relevant) as it relates to documentation clarity, completeness, and correct DRG designation • Coaches physicians to improve their documentation so it more accurately reflects intensity of services and severity of illness • Documents conference and results • Attends various hospital service line meetings, reviewing outcome information, and educating physicians on service line specific improvement opportunities • Complies with HIPAA and Code of Conduct policies • Assists with special projects as needed • Demonstrates competency for individual performance and development in the following areas: Customer Service, Job Skills, Resource Management, Teamwork, and Innovation • Ensures safe care to patients, staff and visitors; adheres to all Memorial Hermann policies, procedures, and standards within budgetary specifications including time management, supply management, productivity and quality of service • Promotes individual professional growth and development by meeting requirements for mandatory/continuing education and skills competency; supports department-based goals which contribute to the success of the organization; serves as preceptor, mentor and resource to less experienced staff

Job Requirements

  • Bachelor of Nursing required
  • Current State of Texas license or temporary/compact license to practice professional nursing
  • Must be an RN with a BSN or MSN
  • Prefer an RN candidate with Clinical Documentation experience
  • Must have at least 5yrs of recent RN bedside experience in an acute hospital setting
  • Must have critical care, ICU nursing experience to be considered
  • Requires excellent observation skills, analytical thinking, problem solving, plus good verbal and written communication
  • Possesses a working knowledge of many areas of adult medicine
  • Able to assess, evaluate, and teach
  • Proficiency in organization and planning
  • Proficiency in computer usage including database and spreadsheet analysis, presentation programs, word processing and Internet searching
  • Ability and willingness to seek out and accept change
  • Demonstrates adaptability, flexibility, and self-motivation, and an ability to work independently
  • Knowledge of federal, state and private payer regulations preferred

Benefits

  • Health insurance
  • 401(k) matching
  • Paid time off
  • Professional development opportunities

Related Categories

Related Job Pages

More Medical writer Jobs

Full TimeRemoteTeam 10,001+H1B Sponsor

• Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and the client authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. • Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations. • Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents. • Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate. • Participate in cross-functional process improvement initiatives. • Participate in defining and writing standard operating procedures and best practices for an efficient preparation of quality documents. • Manage internal and contract medical writing resources as required to ensure timely completion of assigned projects. • Mentor more junior medical writing staff.

Arizona + 4 moreAll locations: Arizona | Maine | New Jersey | Ohio | Rhode Island
$95K - $210.9K / year
Full TimeRemoteTeam 10,001+H1B Sponsor

• The Principal Medical Writer I is responsible for the development of clinical documents for submissions to regulatory authorities globally. • Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents accurately and consistently present key data-driven clinical messages. • Writes or provides direction and leadership to other writers to ensure the timely delivery of high-quality documents that are scientifically rigorous, logically organized, and have accurate data presentation and interpretation. • Oversees the medical writing activities of multiple compounds and serves as lead writer for individual summary documents. • Manage medical writing projects, including developing timelines and communication with cross-functional team members to maintain awareness of review cycles and expectations. • Review other documents associated with the assigned project(s) as appropriate. • Participate in cross-functional process improvement initiatives.

Poland
Full TimeRemoteTeam 10,001+H1B No Sponsor

• The Medical Writer supports client engagements and internal requests, projects, and business development efforts by doing the necessary research, data collection, analysis, and interpretation. • Development of value messages, dossiers, reports and other written deliverables, modeling, educational materials. • Conducting stakeholder and market access research; working with programming and design; and presenting to clients as needed. • Draft content in line with the outline/approach required, in an appropriate style for the deliverable. • Accurate markup references and implementation of directive changes with minimal supervision.

India
Job Closed
Full TimeRemoteTeam 10,001+Since 1956H1B Sponsor

• Serve as primary author for routine documents like clinical study reports and study protocols. • Summarize data from clinical studies. • Assist with more complex clinical and scientific documents. • Ensure compliance with quality processes and requirements. • Assist in program management activities, including timelines, budgets, and forecasts. • Represent the department at project launch and review meetings.

Netherlands