远程工作雷达

临床专员

Clinician Specialist

职能支持限定地区(需当地身份)
公司Centene Corporation
薪资$70,100 - $126,200/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

具备强大的项目管理和组织能力,能够处理多项优先任务并满足监管期限要求。
深入了解利用管理流程、前期授权工具和监管合规要求。
具备出色的沟通能力和利益相关者参与技能,能够与临床、运营、监管和领导层合作伙伴有效协作。
熟练使用数据分析、报告工具和用于跟踪和传达监管及运营信息的软件。
能够在最少指导的情况下独立工作,同时有效应对模糊性和不断变化的优先事项。
持有有效的注册护士执照
标准工作时间为周一至周五,上午8:00至下午5:00。
候选人必须居住在俄克拉荷马州。
该职位支持人口健康与临床运营(PHCO)和医学事务部门。
职位目的:临床专家为部门提供与利用管理和/或病例管理相关的临床和运营支持、指导和方向。该职位负责制定、实施和监控纳入临床指南、政策和/或程序的临床文档,以使部门达到并超越目标,保持监管合规性,提高质量,并促进与临床实践相关的整体效率和效果。

  • 在部门领导和医学主任的指导下,以标准化格式起草临床指南,供部门员工使用,确保符合部门政策和程序。这可能包括起草(或在信息系统中创建新条目)新的临床标准,以及审查现有标准以寻找修改和编辑标准的机会,以确保指南最新,并符合州和联邦指南。
  • 监督和整理以临床为重点的部门标准操作程序(SOP)和政策与程序,确保准确性,并根据需要创建新的标准操作程序,以促进符合州和联邦法规。与部门领导和医学主任合作,协助制定或修改政策与程序。
  • 负责修改或创建成员和供应商信函,包括决定通知和其他监管通知,由部门使用。建议并实施修改
查看英文原文

Strong project management and organizational skills, with the ability to manage multiple priorities and meet regulatory deadlines.
In-depth knowledge of Utilization Management processes, prior authorization tools, and regulatory compliance requirements.
Strong communication and stakeholder engagement skills, with the ability to collaborate effectively with clinical, operational, regulatory, and leadership partners.
Proficiency in data analysis, reporting tools, and software used to track and communicate regulatory and operational information.
Ability to work independently with minimal direction while effectively navigating ambiguity and changing priorities.
An active RN license
The standard schedule is Monday through Friday, 8:00 a.m. to 5:00 p.m.
Candidates must reside in Oklahoma.
This position supports Population Health and Clinical Operations (PHCO) and Medical Affairs.
Position Purpose: The Clinician Specialist provides clinical and operational support, guidance, and direction to the department related to utilization management and/or case management. The position is responsible to develop, implement, and monitor clinical documentation incorporated into clinical guidelines, policies, and/or procedures that will enable the department to meet and exceed goals, maintain regulatory compliance, improve quality, and promote overall efficiency and effectiveness related to clinical practices.

  • Under the direction of departmental leadership and the Medical Directors, draft clinical guidelines in a standardized format to be utilized by department staff that align with departmental policies and procedures. This may including drafting (and/or creating new entries in the information system) new clinical criteria, as well as reviewing existing criteria for opportunities to modify and edit criteria as needed to ensure guidelines are up to date, and in compliance with state and federal guidelines.
  • Monitor and organize the clinical-focused Department Standard Operating Procedure (SOP) and Policy & Procedures to ensure accuracy, creates new standard operating procedures as needed to facilitate compliance with state and federal regulations. Collaborates with Department leadership and Medical Directors to assist in development or modification of policies & procedures as needed.
  • Oversee the modification or creation of member and provider letters, including determination notices and other regulatory notices, utilized by the department. Suggests and implements modifications as necessary to ensure regulatory compliance as well as improved efficiency. Collaborates with internal stakeholders to ensure impacted staff are educated on new policies, procedures, and processes to ensure successful implementation and compliance.
  • Measure and evaluate effectiveness as it relates to current workflows and processes; compare measurement results to standards and work with the team to improve performance and close identified gaps.
  • Research and identify industry best practices and other relevant available published information to contribute to the development of guidelines, policies, and procedures in order to achieve optimal clinical and/or operational outcomes. Develop and maintain documentation necessary to support consistent, operationally sound processes such as tip sheets, standard operating procedures, audit tools.
  • Obtain data and/or run basic reports to determine department performance related to areas of focus, as directed by department leadership. Summarize data for casual analysis or create basic presentations order to communicate progress to management.
  • Job performance requires fulfilling other incidental or related duties as assigned, including but not limited to collaborating with department trainer and supervisory staff in order to plan for implementations and roll out new policies and/or procedures, reviewing regulatory updates, and participating in a variety of department projects.

Education/Experience: MA/MS – Masters Degree preferred. 3-5 years related experience required.
For Clinical Specialist position in Medical Management: Experience with MCG clinical guidelines required.
Prior experience with MCG CareWeb QI guideline modification module preferred.

License/Certification: RN, LMSW, LCSW, LPC, or MHC License required.
For Clinical Specialist position in Medical Management: Licensure as RN required.
Pay Range: $70,100.00 - $126,200.00 per year

At Centene, we connect people to the care they need to live healthier lives — and the work you do here makes that impact real every day. You’ll take on meaningful challenges that directly support individuals, families, and communities, building your skills while making healthcare more accessible and effective. It’s work with a purpose you can see, backed by a team committed to improving lives well beyond the workday.
Centene offers a comprehensive benefits package including: competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility.
Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law.
Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act
Originally posted on Himalayas

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