CrawlJobs Logo

Clinical Educator II - Travel

steris.com Logo

STERIS

Location Icon

Location:
United States , Lexington

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

78200.00 - 101200.00 USD / Year

Job Description:

The Clinical Educator II – Travel ensures that Sterile Processing staff, both internal and external to STERIS, are properly trained and operating within the guidelines set forth by various industry standards and regulations including, but not limited to HSPA, CBSPD, AORN, The Joint Commission, FDA, CDC, DNV OSHA, AAMI and those of STERIS and its customer facilities. Performs various educational duties under supervision and guidance from Manager, Clinical Education, and/or onsite operations leadership. Potential to support and work alongside all instrument processing solutions to include but not limited to continuous improvement, off site reprocessing centers and/or outsourced engagements. Travel positions require up to 100% domestic travel.

Job Responsibility:

  • Design and implement comprehensive training plans aligned with facility priorities and individual staff development needs
  • Collaborate with contracted facilities to ensure every team member is trained to excel at all required competency levels
  • Assess sterile processing staff performance against policies and standard work—identify gaps and deliver impactful training to close them
  • Jump into action with new hire orientation and hands-on training, guided by the Education Management Team or operations leadership
  • Keep training records, education files, and competency documentation organized, accurate, and up to date
  • Maintain a sharp eye on employee certifications and skill levels in the company database—ensuring alignment with job responsibilities
  • Be the go-to expert on multi-specialty instrumentation and a trusted resource for SPD staff
  • Lead re-education efforts and communicate clearly when performance issues arise in the OR or during tray audits
  • Conduct targeted assessments and deliver training that directly addresses identified deficiencies
  • Drive continuous learning by delivering in-services at a cadence set by the Education Manager or leadership
  • Facilitate a comprehensive twelve-week training module for new hires—whether they’re seasoned or brand new to central sterile processing
  • Deliver a full suite of educational modules including Train the Trainer, Onsite Certification, Endoscopy/HLD, Process Improvement Coaching, and more
  • Dive into decontamination, sterilization, and assembly training with confidence and clarity
  • Flex your schedule to support all shifts—day, night, weekend, or evening—to ensure every employee gets the training they need

Requirements:

  • High School Diploma or GED required
  • 5+ years training experience required
  • 5+ years Sterile Processing experience required
  • CRCST (HSPA) or CSPDT (CBSPD) certification required
  • CER (HSPA) or CFER (CBSPD) certification required
  • CIS (HSPA) or CSIS (CBSPD) or CST (NBSTSA) certification required
  • Must maintain certification by completing 12 Continuing Education Credit Hours each year
  • Must maintain valid driver’s license, vehicle insurance and be available to operate a vehicle as needed to meet travel requirements
  • Must be able to travel across the US and pass the Customer’s background and medical standards for credentialing purposes

Nice to have:

  • Associates degree preferred
  • Previous travel experience preferred (1+ year)
What we offer:
  • Bonus participation
  • Comprehensive and competitive benefits portfolio

Additional Information:

Job Posted:
January 30, 2026

Employment Type:
Fulltime
Work Type:
Remote work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Clinical Educator II - Travel

New

Clinical Research Associate II - Multi-Sponsor

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Italy , Milan
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
  • Close to at least 2 years independent monitoring experience in a similar setting
  • Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
  • Sound problem solving skills
  • Able to take initiative and work independently
  • Advance presentation skills
  • Client focused approach to work
  • Flexible attitude with respect to work assignments and new learning
  • Ability to prioritize multiple tasks and achieve project timelines
  • Willingness to work in a matrix environment
Job Responsibility
Job Responsibility
  • Act as PAREXEL's direct contact with assigned sites
  • Build relationships with investigators and site staff
  • Facilitate and support site with access to relevant study systems
  • Evaluate if on-site staff assignment is still accurate
  • Address and resolve issues at sites
  • Follow-up on and respond to appropriate site related questions
  • Apply working knowledge to identify and evaluate potential data quality and data integrity issues
  • Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required
  • Collect, review, and approve updated/amended site documentation
  • Evaluate site recruitment plan
  • Fulltime
Read More
Arrow Right

Clinical Research Associate

CRA II/Senior CRA (Home-based in the U.S.). ICON plc is a world-leading healthca...
Location
Location
United States , Chicago, Portland, Salt Lake City, Blue Bell
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States , LOS ANGELES, PORTLAND, SAN ANTONIO, BLUE BELL, LONG BEACH
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
  • Fulltime
Read More
Arrow Right
New

Administrative Assistant II

The Administrative Assistant is an important part of the business and is the fir...
Location
Location
United States , Alpharetta
Salary
Salary:
Not provided
avanos.com Logo
Avanos
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ years of experience as an administrative assistant supporting multiple teams or functions
  • Highly collaborative, team-oriented professional with strong relationship-building skills and the ability to influence and coordinate across departments
  • Demonstrated ability to work both independently and proactively, showing initiative, sound judgment, and problem-solving skills
  • Strong organizational, time management, and multitasking abilities, with attention to detail and accuracy in record keeping and proofreading
  • Excellent written and verbal communication skills
  • Ability to manage multiple priorities effectively in a fast-paced environment
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint) and related tools (e.g., Adobe Pro) and virtual meeting/teleconferencing tools
  • Familiarity with project coordination, process improvement, or operational support activities
  • Hybrid work arrangement requiring at least three days (Tuesday – Thursday) per week onsite in the Alpharetta office
  • additional onsite presence may be required based on business needs (e.g., audits, shipping requirements, etc.)
Job Responsibility
Job Responsibility
  • Build strong relationships across teams while working both collaboratively and independently to ensure efficient operations
  • Provide administrative support across departments, including expense processing, purchase orders, vendor setup, and supply ordering/shipping
  • Maintain and organize documentation, including SharePoint administration, document control, and reporting of key initiatives
  • Coordinate and manage meetings, and logistics for Quality, Regulatory, Clinical, and Professional Education teams, including preparation of agendas, materials, and meeting minutes
  • Plan and support internal and external events (e.g., Town Halls, business reviews, advisory boards), including venue coordination, catering, materials, and on-site execution
  • Support clinical and professional education activities, including event logistics, asset tracking, shipping, and management (eg., synthetics), and study-related administrative tasks (e.g., invoice reconciliation, enrollment tracking)
  • Support the Laboratory Services group in the coordination of shipping and tracking samples for outside testing
  • Provide on-site support for Quality and Regulatory for both announced and unannounced audits
  • Prepare and assist with documentation for regulatory submissions (publishing support)
  • Assist with budget tracking, forecasting inputs, and report compilation
What we offer
What we offer
  • 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting
  • benefits on day 1
  • free onsite gym
  • onsite cafeteria
  • Fulltime
Read More
Arrow Right

Clinical Studies Coordinator II, Translational Neuroscience

Under departmental direction, coordinates activities to support multiple researc...
Location
Location
United States , Winston Salem
Salary
Salary:
26.55 - 39.85 USD / Hour
advocatehealth.com Logo
Advocate Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree with two years experience in clinical research
  • or an equivalent combination of experience and education
  • SOCRA or ACRP Certification preferred
  • Must complete the CITI certification for Human Subject Research if not already completed
  • All additional required WakeOne training for research coordinators
  • Excellent interpersonal, oral, and written communication skills
  • Excellent reading comprehension
  • Strong organizational skills
  • EPIC/WakeOne proficiency to include appropriate documentation of research notes
  • Proficient in the use of OnCore/WISER Clinical Trial Management System
Job Responsibility
Job Responsibility
  • Coordinates activities to support multiple research studies of all phases
  • Serves as the principal administrative liaison for assigned studies
  • Develops and maintains recordkeeping systems and procedures to ensure compliance
  • Attends clinic as needed to perform activities including recruitment, administering questionnaires
  • Responsible for the compilation, registration and submission of data
  • Works under the direction of the Study Investigators or Clinical Research Nurse Manager
  • Plays an active role in recruitment of patients to study
  • Performs protocol specific duties required per the research protocol
  • Obtains or assists the Principal Investigator in obtaining informed consent
  • Fulfills sponsor requirements related to reportable information including adverse events
What we offer
What we offer
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Opportunity for annual increases based on performance
  • Premium pay such as shift, on call, and more
  • Incentive pay for select positions
  • Fulltime
Read More
Arrow Right

Clinical Studies Coordinator II, Translational Neuroscience

Under departmental direction, coordinates activities to support multiple researc...
Location
Location
United States , Winston Salem
Salary
Salary:
26.55 - 39.85 USD / Hour
advocatehealth.com Logo
Advocate Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree with two years experience in clinical research
  • or an equivalent combination of experience and education
  • SOCRA or ACRP Certification preferred
  • Must complete the CITI certification for Human Subject Research if not already completed
  • All additional required WakeOne training for research coordinators
  • Excellent interpersonal, oral, and written communication skills
  • Excellent reading comprehension
  • Strong organizational skills
  • EPIC/WakeOne proficiency to include appropriate documentation of research notes
  • Proficient in the use of OnCore/WISER Clinical Trial Management System
Job Responsibility
Job Responsibility
  • Coordinates activities to support multiple research studies of all phases
  • Serves as the principal administrative liaison for assigned studies
  • Develops and maintains recordkeeping systems and procedures to ensure compliance
  • Attends clinic as needed to perform activities including recruitment, administering questionnaires
  • Responsible for the compilation, registration and submission of data
  • Works under the direction of the Study Investigators or Clinical Research Nurse Manager
  • Plays an active role in recruitment of patients to study
  • Performs protocol specific duties required per the research protocol
  • Obtains or assists the Principal Investigator in obtaining informed consent
  • Fulfills sponsor requirements related to reportable information including adverse events
What we offer
What we offer
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Opportunity for annual increases based on performance
  • Premium pay such as shift, on call, and more
  • Incentive pay for select positions
  • Fulltime
Read More
Arrow Right
New

Care Management Specialist II

Established in 1997, L.A. Care Health Plan is an independent public agency creat...
Location
Location
United States , Los Angeles
Salary
Salary:
88854.00 - 142166.00 USD / Year
lacare.org Logo
L.A. Care Health Plan
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associate's Degree in Nursing for Registered Nurses
  • Master's Degree in Social Work for Licensed Clinical Social Workers
  • Minimum of 3 years of recent care management experience with responsibilities of managing complex acute or chronic conditions in collaboration with members and interdisciplinary care professionals in a hospital, medical group or managed care setting, such as a health insurance environment and/or experience as care manager in home health or hospice environments
  • Experience providing care management with complex/catastrophic conditions
  • Current knowledge of clinical standards of care and disease processes
  • Critical thinking skill
  • Excellent customer service skills
  • Ability to clinically analyze the most complex cases involving highly acute physical health, behavioral health, complex/catastrophic and/or psychosocial issues to determine and implement the most effective member-centered interventions
  • Ability to triage immediate member health and safety risks
  • Ability to sensitively manage member or family responses associated with high acuity cases and support effective coping
Job Responsibility
Job Responsibility
  • Applies clinical knowledge and experience to evaluate information regarding prospective care management members referred by health risk assessment (HRA), risk stratification, predictive modeling, provider’s utilization review vendors, members, Call Center, claims staff, Health Homes Program (HHP) eligibility or other data sources to determine whether care management intervention is necessary to meet the member's needs
  • Conducts Care Management services for the most complex and vulnerable members including: engaging in member centric communication which includes the interdisciplinary team, providers and family or authorized representatives
  • reviewing member claims histories and identifies intervention opportunities through the professional standards of practice
  • contacting and interviewing members to conduct a baseline assessment, assess self-care ability, assess knowledge and adherence deficits
  • conducting comprehensive clinical assessments as indicated
  • developing a member centric plan of care. Maintains assigned care management caseload for with a focus on the most complex, highest-risk members particularly those with advanced chronic conditions, co-occurring mental and/or substance abuse and complex social issues (e.g. homelessness, domestic violence)
  • Collaborates with primary care physician and other treating professionals as appropriate. Authorizes initiation of care management services and specialized program services for members and specific populations, and develops interventions designed to meet member or population desired outcomes. Provides comprehensive education and resources to members about accessing services, in-network use, national guidelines for care, community resources, and self-management skills and strategies
  • Employs engagement techniques to build relationships with members and their authorized representatives. Encourages participants to participate in their health care decisions and assists member with researching treatment options in order to communicate effectively with providers and to make informed decisions
  • Notifies Care Coordinators and CHWs of members needs including the need for special educational mailings, reminder calls, satisfaction surveys, incentives or any additional service needs according to specific program guidelines
  • Performs field assessment and care coordination functions in community settings with members, such as at the L.A. Care Community Resource Centers, medical clinics, and member homes
What we offer
What we offer
  • Paid Time Off (PTO)
  • Tuition Reimbursement
  • Retirement Plans
  • Medical, Dental and Vision
  • Wellness Program
  • Volunteer Time Off (VTO)
  • Fulltime
Read More
Arrow Right

Care Management Specialist II, D-SNP Team

The Care Management Specialist II utilizes clinical skills and training to perfo...
Location
Location
United States , Los Angeles
Salary
Salary:
88854.00 - 142166.00 USD / Year
lacare.org Logo
L.A. Care Health Plan
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associate's Degree in Nursing for Registered Nurses OR Master's Degree in Social Work for Licensed Clinical Social Workers
  • Minimum of 3 years of recent care management experience with responsibilities of managing complex acute or chronic conditions in collaboration with members and interdisciplinary care professionals in a hospital, medical group or managed care setting, such as a health insurance environment and/or experience as care manager in home health or hospice environments
  • Experience providing care management with complex/catastrophic conditions
  • Current knowledge of clinical standards of care and disease processes
  • Critical thinking skill
  • Excellent customer service skills
  • Ability to clinically analyze the most complex cases involving highly acute physical health, behavioral health, complex/catastrophic and/or psychosocial issues to determine and implement the most effective member-centered interventions
  • Ability to triage immediate member health and safety risks
  • Ability to sensitively manage member or family responses associated with high acuity cases and support effective coping
  • Strong verbal and written communications skills to consult effectively with interdisciplinary teams, coordinate care with members and their families, and other internal and external stakeholders
Job Responsibility
Job Responsibility
  • Utilizes clinical skills and training to perform essential functions of care management for identified and assigned member population according to Health Insurance Portability and Accountability Act (HIPAA) guidelines
  • Manages a specified caseload across the entire continuum of programmatic levels including those within National Committee for Quality Assurance (NCQA) scope or otherwise Complex/Catastrophic cases
  • Management of the caseload assigned by Manager includes: coordinating health care benefits, providing education and facilitating member access to care in a timely and cost-effective manner
  • Collaborates and communicates with member, family, and interdisciplinary health team to promote wellness and member empowerment, while ensuring access to appropriate services across the healthcare continuum and maximizing member benefit
  • Serves as clinical advocate for members, active interdisciplinary team member, liaison with other departments and external health care team
  • Provides direction and assistance to Care Coordinators and to Community Health Workers (CHW) of members needs including the need for special educational mailings, reminder calls, satisfaction surveys, incentives or any additional service needs according to specific program guidelines
  • Uses claims processing and care management software to look up member information, document contacts, and track member progress
  • Applies clinical knowledge and experience to evaluate information regarding prospective care management members referred by health risk assessment (HRA), risk stratification, predictive modeling, provider’s utilization review vendors, members, Call Center, claims staff, Health Homes Program (HHP) eligibility or other data sources to determine whether care management intervention is necessary to meet the member's needs
  • Conducts Care Management services for the most complex and vulnerable members including: engaging in member centric communication which includes the interdisciplinary team, providers and family or authorized representatives
  • reviewing member claims histories and identifies intervention opportunities through the professional standards of practice
What we offer
What we offer
  • Paid Time Off (PTO)
  • Tuition Reimbursement
  • Retirement Plans
  • Medical, Dental and Vision
  • Wellness Program
  • Volunteer Time Off (VTO)
  • Fulltime
Read More
Arrow Right