20 Best Director Of Regulatory Affairs jobs (Hiring Now!)

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Assistant Director, Science , Regulatory and Advocacy
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Director of Policy and Regulatory Affairs
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Director of Government and External Affairs
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Government Affairs Director
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Director of Credentialing
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17h

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Medical Staff Quality Specialist

Charleston Area Medical Center (CAMC) - Charleston, WV

Quick Apply

Job Details

Full-time Estimated: $60.5K - $76.6K a year

Qualifications

Nursing
Medicine
RN License
5 years
Microsoft Office
Compliance management
Bachelor's degree
Senior level
Documentation review
Nursing

Full Job Description

CAMC is seeking a Medical Staff Quality Specialist to join the Medical Affairs Team.

The Medical Staff Quality Specialist will support the Vice President for Medical Affairs for provision of expertise and facilitation to elected Medical Staff leaders, Medical Staff committee chairs, and Clinical Directors for carrying out their oversight accountabilities for the quality of medical care in conformance with the medical staff governing documents, accrediting body accreditation standards, Health Care Quality Improvement Act (HCQIA), and pertinent regulatory and legislative requirements.

Responsibilities

Support the Chair of the Committee for Professional Enhancement (peer review) in agenda development, triage of case reviews, minutes and communication with Clinical Quality Specialist. Prepare CPE report to MEC. • Function as a resource and partner to the Clinical Quality Specialist in development, guidance and presentation of indicators to the Committee for Professional Enhancement (peer review). • Responsible for triage of patient complaints, grievances, safety reports and other intakes of issues related to credentialed providers. Conduct fact finding reviews, timeline preparations when necessary chart reviews and presentation to the leadership council for recommendations and actions taken. • Responsible for the management and development of ongoing professional practice evaluations for eight(8) medical staff departments and occasional support for the other departmental medical staff quality specialist as needed. Develop appropriate quality indicators and scorecards (OPPE) for the individual providers on an annual basis within assigned departments and understand triggers that would prompt additional department chief review and consideration of next steps. • Attend Credentials Committee planning and Credentials Committee meeting to validate new applicants coming through the process in order to familiarize with the applicant and obtain awareness of any special privileges that would require proctoring. • Collaborate with the credentials manager to oversee the proctoring process in for all provider as applicable in eight (8) departments. Prepare appropriate documents timely and provide to Credentials Department as completed reports for review by the medical staff. • Coordinate and provide support to the Chief of Staff Investigative Committees in concordance with the Medical Staff Governing Documents, HCQIA and Medical Staff procedures. • Collaborate with Risk Management (Patient Safety) and Office of General Counsel reporting incidents/occurrences, which may result in professional liability claims. • Manage and improve software capabilities working with the provider data management specialist to include management of peer review, OPPE and other key processes critical to the work of the quality specialist. • Manage referrals to external peer review agencies in coordination with the medical staff, medical records and other key departments. • Attend accreditation survey sessions to present process and provider data as appropriate to the review being conducted. • Responsible for serious adverse event call annually (avg. 3-4 times per year) • Train and participate in internal auditing procedures through the regulatory office. • Attend and support all medical staff committees as assigned. • Coordinate, review and develop responses to Third Party Payer/Insurance Reviews/Compaints. • Maintain credentialed provider health records as needed. • Work in collaboration with Trauma Coordinators to ensure Peer Review policy is followed. • Serves as M&M committee resource to assure compliance with Medical staff governing documents. • Software experience preferred: RLDatrix, MD STAFF, MD STAT, Cerner Lights on, Premier Physician Focus, Cerner, and Microsoft Office.

Qualified applicants will have a Bachelor's Degree in a related field and 5-10 years experience in clinical nursing, performance improvement and medical staff and/or organizational committee/ activities.

Apply online at camc.org/careers for JOB ID#35356: https://gen-camc-prd.inforcloudsuite.com/hcm/xmlhttp/shorturl.do?key=NOZ

Equal Opportunity Employer

Job Type: Full-time

Schedule:

Day shift
Monday to Friday

Education:

Bachelor's (Required)

Experience:

clinical: 5 years (Required)

Work Location: In person

Quick Apply

Director Of Regulatory Affairs jobs

Medical Staff Quality Specialist

Director of Analytical

Regulatory Affairs Director

Pediatric Clinic Director, ABA Services

Protective Services Regional Program Director

Director, Global Medical Affairs Strategy - Solid Tumors

QIDP / Program Director

Director of Regulatory Affairs, Regulatory Affairs, Full Time

Senior Director, US Medical Affairs Solid Tumor Portfolio

Land Entitlement Director

Nuclear Med Technologist Coord

Assistant Director, Science , Regulatory and Advocacy

Director of Policy and Regulatory Affairs

Director of Government and External Affairs

Executive Director Market Access Pipeline

Regulatory Affairs Director (Hybrid - 3 Days in Office - VA)

Government Affairs Director

Director of Regulatory Affairs

Director, Legal and Regulatory Affairs

Director of Credentialing

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