CrawlJobs Logo

Senior Manager Clinical Eligibility

United States, New York · Job Posted May 03, 2026
Apply Position
Job Link Share

Job Description

The Senior Mgr of Clinical Eligibility will have knowledge of the current assessment process, for both Medicaid and Medicare programs. This position will support the Assessment Managers in planning, directing, and implementing processes for successful outcomes and achieving goals. The Sr Mgr conducts and contributes to member and family education regarding health management and community resources to enhance population health. This position will be responsible for the overall administration, development, and operation of the Assessment team.

Job Responsibility

  • Participates in all aspects of personnel management to ensure appropriate staffing, orientation, support, discipline, and timely performance appraisals
  • Meets regularly with direct reports to review goals, trends, and performance measures and to facilitate change
  • Participates in continued staff development to improve the decision-making process
  • Provides administrative on-call coverage to troubleshoot and coordinate the delivery of care and services to members
  • Manages Assessment Managers to ensure timely assessments and targeted interventions to meet a member's changing condition(s)
  • Supports the care management teams to ensure effective care management and oversight of home vendor services
  • Supervises and directs the completion of assessments at established intervals to coincide with care plan development/revision and ensures early identification and action to address emergent issues
  • Assists members and prospective members with assessment and clinical eligibility questions
  • Coordinates with contract services to ensure understanding of the MLTC model, FIDA, MAP, and MMCP and cooperation with the assessment process
  • Ensures coordination with home health, nursing, and social work care as it relates to the care plan
  • Facilitates problem solving by coordinating case conferences and investigations with the care teams
  • Functions as a facilitator for the team and managers to ensure smooth workflow, efficiency and success within the four programs: PHSP, CC, AE, and SHP
  • Functions as a liaison to ensure process coordination with different organizational departments such as Intake/Medical Records/CMT/IT/HR/Marketing
  • Additional duties as assigned

Requirements

  • NYS licensed RN
  • Knowledgeable of state and federal regulations including experience interpreting those regulations as it pertains to different programs
  • Excellent interpersonal skills, especially relating well with a frail adult population, their families and community care providers, along with demonstrated ability to handle rapidly changing crisis situations while still achieving department goals and objectives
  • Understanding of and sensitivity to cultural differences and needs of the community are essential with a diverse and multi-cultural work environment and community of members such as Spanish, Chinese, Russian, Creole and Korean
  • Language preferences - Spanish, Russian, French, Creole, Mandarin, Cantonese
  • Bachelor's degree
  • Intermediate Microsoft Word, Excel, Outlook, Powerpoint, Access, Adobe, Visio, and project skills
  • Proficient navigating internet browsers, computer hardware, and multiple applications simultaneously, using encryption security tools, multiple electronic PHI databases, working in with a VPN and Citrix platform and very accurate typing skills
  • Demonstrated professionalism and leadership skills along with the ability to develop, direct, and support staff
  • Experience in home care environment, acute, sub-acute or long term care (LTC) setting or managed-long term care (MLTCP)
  • Experience in one of these areas: managed care organization, PACE, MLTCP, CHHA, licensed agency or a Lombardi program
  • Excellent communication, time management, writing, critical thinking, and problem solving skills
  • Supervisory, training, or management experience

Nice to have

  • Knowledgeable of state and federal regulations including experience interpreting those regulations as it pertains to different programs
  • Excellent interpersonal skills, especially relating well with a frail adult population, their families and community care providers, along with demonstrated ability to handle rapidly changing crisis situations while still achieving department goals and objectives
  • Understanding of and sensitivity to cultural differences and needs of the community are essential with a diverse and multi-cultural work environment and community of members such as Spanish, Chinese, Russian, Creole and Korean
  • Language preferences - Spanish, Russian, French, Creole, Mandarin, Cantonese
  • Bachelor's degree
  • Intermediate Microsoft Word, Excel, Outlook, Powerpoint, Access, Adobe, Visio, and project skills
  • Proficient navigating internet browsers, computer hardware, and multiple applications simultaneously, using encryption security tools, multiple electronic PHI databases, working in with a VPN and Citrix platform and very accurate typing skills
  • Demonstrated professionalism and leadership skills along with the ability to develop, direct, and support staff
  • Experience in home care environment, acute, sub-acute or long term care (LTC) setting or managed-long term care (MLTCP)
  • Experience in one of these areas: managed care organization, PACE, MLTCP, CHHA, licensed agency or a Lombardi program
  • Excellent communication, time management, writing, critical thinking, and problem solving skills
  • Supervisory, training, or management experience

What we offer

  • medical, dental and vision coverage
  • incentive and recognition programs
  • life insurance
  • 401k contributions

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Senior Manager Clinical Eligibility

8 matching positions

Senior Clinical Manager

Compass Associates are proud to be partnering with a specialist medico-legal reh...
Location
Location
United Kingdom , London
Salary
Salary:
65000.00 GBP / Year
compass-associates.com Logo
Compass Associates
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive experience within medico-legal case management, including IRCM registration or eligible for this
  • Previous senior clinical leadership or operational management experience
  • Experience overseeing governance, quality standards, and MDT working
  • Experience managing referrals, budgets, and operational responsibilities
Job Responsibility
Job Responsibility
  • Provide day-to-day clinical and operational oversight across the London & South region
  • Maintain governance, compliance, and quality standards
  • Oversee referrals and new business enquiries
  • Retain a small caseload where appropriate
  • Support regional growth and service development
  • Contribute to operational planning and innovation
  • Lead, supervise, and support clinical managers and case management teams
  • Support professional development and performance standards
  • Represent the organisation at industry events and networking forums
What we offer
What we offer
  • Mileage paid at 45p per mile
  • Business expense reimbursement (travel, accommodation)
  • 25 days annual leave + bank holidays (rising to 30 with service)
  • Private healthcare
  • Employee Assistance Programme
  • Company pension scheme
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
South Korea
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Fluent in English and in the native language(s) of the country they will work in
  • Extensive knowledge of clinical trial methodologies, ICH/GCP and local country regulations
  • Global clinical trial experience
  • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
  • Demonstrated knowledge of clinical research and development processes
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research
  • Demonstrated knowledge in disease and technical areas pertaining to clinical studies
  • Demonstrated ability to support sponsor regulatory interactions/inspections
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
  • Serve as the primary point of contact for assigned investigator sites
  • Interface with the study team as needed
  • Partner with SCP to perform investigator site development, coaching and training of site personnel
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs)
  • Submit all required reports, documentation, updates and tracking within required timeframes
  • Identify and resolve investigator site issues within required timeframes
What we offer
What we offer
  • Patient-focused culture
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate - Midwest/Central US - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Bachelor's degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Ability to travel 60-80%
  • Valid driver's license and passport required
Job Responsibility
Job Responsibility
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs)
  • Submit all required reports, documentation, updates and tracking within required timeframes
  • Identify and resolve investigator site issues within required timeframes
  • Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate/Clinical Research Associate II - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
  • Preferred therapeutic experience in Oncology
  • Global clinical trial experience preferred
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Travel (60-80%) within area is required
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites
  • Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • Provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F)
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
  • Partner with SCP and the study team to define and support recruitment initiatives at site level
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Argentina
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Global clinical trial experience
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
What we offer
What we offer
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Senior Clinical Research Specialist

As a community, the University of Rochester is defined by a deep commitment to M...
Location
Location
United States of America , Rochester
Salary
Salary:
60431.00 - 84603.00 USD / Year
urmc.rochester.edu Logo
University of Rochester
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree and 3 years of relevant experience required
  • Ability to effectively manage complex research protocols/procedures required
  • Fully adheres to applicable safety and/or infection control standards
  • Proficiency in medical terminology, the clinical research process, and applicable regulatory guidelines, standards preferred
  • Proficiency in managing multiple and competing priorities/demands
  • Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, and OSHA guidelines throughout study implementation
  • Exceptional interpersonal, organizational, and time management skills
  • highly collaborative, promotes teamwork
  • Ability to build collaboration among research team members, laboratory staff, patients, and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients)
  • Proficient in MS Office (e.g., Word, Excel, and PowerPoint), email, and internet
Job Responsibility
Job Responsibility
  • Provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols
  • Manages the day-to-day operations of multiple studies, carrying out study coordination duties from protocol development and initiation through to study close-out in accordance with regulatory/sponsor guidelines
  • Monitors and maximizes adherence to research standards, regulatory guidelines, and approved operational procedures
  • Works closely with study team members and other study sites to ensure the safety and adherence of study participants to the study protocol
  • Manages study-related administrative and human resources tasks and facilitates across-the-board flow of information, orchestrating study activities and personnel
  • Coordinates enrollment of participants
  • Oversees and facilitates eligibility screening and study recruitment activities
  • Plans study timelines and schedules appointments and study visits
  • Manages and organizes case report forms, source documents, and research records
  • Enters research data into data collection forms and/or study databases
  • Fulltime
Read More
Arrow Right

Senior Clinical Practice Integration Specialist

The Senior Clinical Practice Integration Specialist plays a vital role in streng...
Location
Location
United States , Oconomowoc
Salary
Salary:
Not provided
rogersbh.org Logo
Rogers Behavioral Health
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree preferred in Counseling, Psychology, Social Work, Marriage and Family Therapy, or a related behavioral health field from an accredited program
  • Equivalent experience will be considered, including candidates with a Bachelor’s degree combined with an advanced substance use disorder credential (e.g., SAC, CADC, LADC or equivalent) and significant clinical and practice-based experience in behavioral health settings
  • Active clinical credential or license, or eligibility for credentialing/licensure as applicable to role scope, with the ability to meet organizational and state requirements
  • Minimum of 5+ years of progressive experience in behavioral health clinical care, with demonstrated involvement in practice implementation, training, supervision, or quality improvement initiatives
  • Demonstrated expert knowledge of therapist workflow, clinical documentation standards, and minimum regulatory and licensing requirements, including substance use–related regulations, accreditation standards, and payer expectations
  • Proven experience in clinical care delivery, training, and supervision
  • Strong interpersonal skills are needed to interact with patients and professional staff
  • Must be able to work independently and complete assignments within specified time frames
  • Must be able to read and communicate through written, verbal, and auditory skills and abilities
  • Physically/Mentally able to perform job duties as verified by a physical exam by a licensed physician, per post-employment physical
Job Responsibility
Job Responsibility
  • Deliver comprehensive onboarding and ongoing training for direct-care clinicians
  • Provide training that integrates evidence-based practices, regulatory standards, care pathways, and documentation requirements
  • Maintain and update training materials to reflect best practices, licensure standards, accreditation expectations, and organizational policies
  • Offer re-training, consultation, and just-in-time training to strengthen clinician skill development and treatment fidelity and support coaching to standards
  • Support training and development for clinical leaders (e.g., clinical supervisors, managers)
  • Support training and development for undergraduate interns/practicum students
  • Train clinicians on the practical use of clinical technologies that support documentation, workflow efficiency, patient engagement, and treatment delivery
  • Ensure staff understand how technology intersects with clinical models, documentation standards, and regulatory expectations
  • Provide frontline support and troubleshooting related to clinical technology use
  • Monitor the use of technology to identify training needs, skill gaps, and opportunities to enhance clinical efficiency or accuracy of documentation
What we offer
What we offer
  • Health, dental, and vision insurance coverage for you and your family
  • 401(k) retirement plan
  • Employee share program
  • Life/disability insurance
  • Flex spending accounts
  • Tuition reimbursement
  • Health and wellness program
  • Employee assistance program (EAP)
  • Fulltime
Read More
Arrow Right

Senior Clinical Dietitian

Montefiore has a rare opportunity for a Senior Clinical Dietitian to join our we...
Location
Location
Australia , Randwick; Hunters Hill; Woollahra
Salary
Salary:
Not provided
montefiore.org.au Logo
Montefiore
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor or postgraduate degree in dietetics (or nutrition and dietetics) or equivalent
  • Eligibility for full membership with Dietitians Australia
  • Minimum of five years' experience
  • Previous experience providing clinical supervision
  • Able to work autonomously and as part of a team
  • Effective time management/prioritisation skills
  • Excellent written and verbal communication skills
  • Ability to build effective relationships in an interdisciplinary setting
  • Willingness to travel across sites as per operational requirements
Job Responsibility
Job Responsibility
  • Provide visible leadership and support to the Dietetics and Dietary Coordinator team in quality improvement, policy alignment and governance functions
  • Provide advanced clinical dietetic care for residents with complex nutrition needs
  • Lead and model best practice clinical dietetic care for residents with complex nutrition needs, while supporting other team members through case discussion, mentoring and supervision
  • Work closely with the Dietetics and Speech Pathology Manager on service development, orientation and training, and alignment with the Montefiore Experience and organisational policies
  • Build strong relationships with Clinical and Catering Teams to ensure coordinated, person directed food, nutrition and mealtime care across all neighbourhoods and sites
  • Participate in projects that enhance resident wellbeing and align with our core values of Choice, Dignity, and Respect
What we offer
What we offer
  • Ongoing access to training and development opportunities
  • Competitive remuneration package that includes NFP salary packaging
  • Generous leave entitlements
  • Highly supportive workplace culture with a genuine passion for continuous improvement and excellence
  • Parttime
Read More
Arrow Right