Speech Language Pathology Assistant - Cross Country Education

Similar jobs

• Edlogical Group, A Member of the Point Quest Group

  

  Resource Specialist Teacher

  4 days ago

  Los Angeles

  Resource Special Education Teacher Key Responsibilities: • Supports student engagement and learning through development of lesson plans, implementation of accommodations, visual supports, and consulting with general education teacher as needed., • Administer, transfer, and interpret educational assessment data for supporting educational decision making and goal development, • Establish and maintain standards of student behavior to achieve a functional learning atmosphere., • Adapt the curriculum with individual plans and instructional materials to the needs of each student according to their IEP., • Maintains documentation on IEP goals, student academic and social growth, and prepares progress reports., • Maintain a program inventory of materials and supplies., • Promotes inclusion opportunities for students and collaborates with general education teachers as appropriate to student needs., • Maintain accurate and compliant paperwork for IEP caseload including quarterly progress reports., • "STATE" Department of Education Teaching Certificate for Special Education, • Department of Justice/FBI Background Check, • TB Clearance, • Eligibility to work in the US, • Preferred Qualifications:, • Experience with school-based services and accommodations, • Occasional exposure to dust, pollen, and/or fumes., • Frequent reaching, handling, sitting, standing, walking, hearing, talking, stooping, bending, crouching, kneeling, running, carrying, and lifting up to 50 pounds. PQI is an Equal Opportunity Employer and considers all qualified applicants regardless of race, gender, color, religion, national origin, age, sexual orientation, gender identity, disability, veteran status, or other classification protected by law.

• Edlogical Group, A Member of the Point Quest Group

  

  Teacher for the Visually Impaired

  2 days ago

  Los Angeles

  • Student Evaluation & Assessment: Use criterion and norm-referenced tests to assess pupils' visual functioning, communication, motor, social, self-help, academic, vocational, and cognitive skills. Determine eligibility and appropriate placement., • IEP Development: Create and implement individualized education plans (IEPs) with measurable goals and objectives based on assessments, child development principles, and learning continuums., • Instruction & Integration: Teach specialized skills, including braille, orientation and mobility, and use of visual aids. Facilitate student integration into regular education programs and assist in explaining disabilities., • Curriculum & Consultation: Develop and deliver curriculum activities that align with students' objectives. Provide consultation and resources to regular classroom teachers., • Classroom Management: Maintain a positive learning environment, monitor student progress, and adjust teaching strategies as needed. Prepare and execute daily lesson plans, utilizing diverse materials and techniques., • Documentation & Compliance: Accurately complete records and ensure compliance with state regulations and timelines. Attend required meetings and share materials with colleagues., • Physical & Mental Requirements: Demonstrate physical stamina, dexterity, and mobility for classroom activities, emergency situations, and itinerant assignments. Maintain mental acuity for data interpretation and problem-solving., • Additional Duties: Fulfill other assigned responsibilities as needed., • Education & Credentials: Bachelor's Degree from an accredited institution. Education Specialist credential in Visual Impairment., • Specialized Skills: Each candidate demonstrates the use of common specialized media devices such as closed circuit television, tape recorder, word processors with large print displays, Braille, or voice output capabilities, electronic note takers adaptive materials such as a talking calculator and tactile graphics, understands the psychological, sociological and vocational implications of visual impairment. In addition, each candidate demonstrates knowledge of the vocational implications resulting from attitudes toward visual impairment., • Certifications: First Aid and CPR Certification within six months of employment. DOJ/FBI Live Scan Background & TB Clearance required. Pro-Act, CPI, and/or additional CPR certifications are helpful., • Abilities: Valid California driver's license and insurability. Strong organizational and planning skills with the ability to interact professionally with staff and the public. Effective oral and written communication in English., • Desirable Experience: Experience working with children with visual impairments (birth through 21 years) and severe disabilities. Teaching experience in general education settings and proficiency in Sign Language or bilingual skills., • Environment: Occasional exposure to dust, pollen, and fumes., • Activity: Frequent engagement in tasks such as reaching, handling, standing, walking, and lifting items, with or without reasonable accommodations. PQI is an Equal Opportunity Employer and considers all qualified applicants regardless of race, gender, color, religion, national origin, age, sexual orientation, gender identity, disability, veteran status, or other classification protected by law.

• American Career College

  

  Adjunct OB Clinical Instructor-ADN Program

  6 days ago

  Los Angeles

  At American Career College, we share a.As a faculty member for a certified Great Place to Work, you will join a collaborative, student-centric culture valuing academic integrity, mutual respect, student learning, service, responsiveness, innovation, diversity, and stewardship.As a part of this team

• UCLA Health

  

  Paramedic Clinical Instructor - Center for Prehospital Care

  2 days ago

  Los Angeles

  Description The UCLA Center for Prehospital Care (CPC) is the leading emergency and prehospital academic center on the West Coast. The Center is dedicated to advancing the systems and methods of EMS. We teach, test, and certify the people who provide care to the ill or injured prior to hospital admission. Clinical Instructors provide skills presentations and skills instruction in the UCLA Paramedic Education Program and must work a minimum of two shifts per month. Responsibilities include but are not limited to: • Providing demonstrations and instructing on the application of equipment, • Monitor student performance of practical skills, • Being a student advocate in the learning process, • Creating an active learning environment, • Ensuring course requirements and objectives are met, • Assisting in the development of educational objectives as well as testing methods This is a 10% per diem position. May convert to career. Salary: $31.51 - $62.64 hourly Qualifications Required: • Current California licensure as a Paramedic or Registered Nurse or the ability to obtain licensure in the state of CA., • Minimum of 1 year of field or clinical EMS experience., • Ability to consistently work a minimum 2 weekdays per month., • Excellent communication skills., • Ability to work both independently and on a team., • Ability to perform duties with minimal direction., • The instructor may be required to perform venipuncture and dermal punctures on training equipment including administering intravenous lines., • Available to meet scheduling requirements to include evenings, holidays, and/or weekends., • Ability to foster a stimulating classroom environment., • Skill in working independently and following through with minimal direction., • Skill in working as part of a team collaborating with colleagues., • Ability to provide service oriented customer assistance in a professional and courteous manner., • Interpersonal skills to excel in relations supervisor, staff, students, and the public., • Previous teaching experience., • AHA CPR provider certification, AHA ACLS provider certification AHA ACLS and/or PALS instructor certifications., • NAEMT PHTLS instructor certifications.

• CEDARS-SINAI

  

  Clinical Research Associate II - Women's Research Program - Full-Time, On-Site

  2 days ago

  Los Angeles

  Job Description Come join our team! The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to coordinate and/or implement increasingly complex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines. Provides increasingly complex and independent support for studies by serving as the independent contact with sponsors, IRB, and research participants, providing training, education to junior level staff, and coordination of ad hoc activities related to studies. May serve independently as study coordinator for minimal number of noncomplex research studies or projects. What are the Primary Duties & Responsibilities? • Works independently under minimal direction from a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to coordinate and/or implement increasingly complex research studies., • Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors., • Completes Case Report Forms (CRFs)., • Independently prescreens potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. May provide increasingly independent contact with research participants and/or conduct research participant visits independently., • Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, Safety Letters, etc in accordance with local and federal guidelines., • Assists with clinical trial budgets and patient billing., • Responsible for sample preparation and shipping and maintenance of study supplies and kits., • Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local IRB. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law., • May serve as the primary point of contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities., • Participates in and provides training and education to other Clinical Research Associates. May assist in coordinating activities of other associates to ensure compliance with protocol and clinical research objectives., • Participates in centralized activities such as auditing, Standard Operating Procedure development, etc., • May participate in the development of Investigator Initiated trials for Investigational New Drug applications and/or Device applications, • High School Diploma/GED required. Bachelor's Degree in Science, Sociology or related degree preferred., • One (1) year of clinical research related experience required

• CEDARS-SINAI

  

  Clinical Research Associate I - Medically Associated Science & Technology (MAST) Program

  24 hours ago

  Los Angeles

  Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity! As a Clinical Research Associate I, you will work under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of non-complex research studies. The incumbent will support objectives of research studies through non-complex tasks such as data collection, pre-screening and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines. Primary Job Duties and Responsibilities: • Collects, evaluates and/or abstracts clinical research data., • May assist in designing forms for data collection/abstraction., • Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors., • Completes Case Report Forms (CRFs)., • Schedules research participants for research visits and research procedures., • Provides supervised patient contact or independent patient contact for long term follow-up patients only., • Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines., • Assists with clinical trial budgets and patient research billing., • Responsible for sample preparation and shipping and maintenance of study supplies and kits., • Ensures compliance with protocol and overall clinical research objectives., • Maintains research practices using Good Clinical Practice (GCP) guidelines., • Maintains strict patient confidentiality according to HIPAA regulations and applicable law., • May serve as one point of contact for external sponsors for select trials., • Maintains CITI certification., • Compiles, analyzes, and presents work at internal meetings and conferences., • Performs data searches and other related administrative tasks., • Assists with research protocol writing and development., • Assists with prescreening of research participants for various clinical trials., • Attends research meetings and monthly conference calls with sponsors., • Maintains organized paper and electronic research files., • Performs all data collection and data entry tasks for departmental clinical studies., • Assists with preparing manuscripts, letters, and other research documents as needed., • High School Diploma/GED is required.

• CEDARS-SINAI

  

  Clinical Research Data Associate III - The Angeles Clinic & Research Institute

  8 days ago

  Los Angeles

  Job Description Grow your career at Cedars-Sinai! The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer. Join our team and contribute to groundbreaking research! The Clinical Research Data Associate III manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. In addition, may supervise clinical research staff or clinical data managers, perform complex statistical analysis, and work with bioinformatics to develop and maintain trial management and validation systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Primary Duties and Responsibilities: • Supervise clinical research data specialists, as needed., • Work with bioinformatics in the development and maintenance of clinical trials management systems including validation of systems, as needed., • Train clinical research staff to help improve the quality of the data being collected, as needed., • Solve operational/data problems in consultation with other employees and/or supervisors, as needed., • Plans and prepares the team for study audits and delegates task to team members to ensure audit readiness., • Participates in the study audit process and coordinates the necessary follow up with the study team., • Coordinates data for research studies., • Designs forms for data collection., • Performs clinical data collection/abstraction., • Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data., • Produces project reports., • Performs data searches and other related administrative tasks., • Participates in required training and education programs., • Works closely with study monitors to review study data and respond to inquiries. Department-Specific Responsibilities: • Will be responsible for translating research questions into analytic plans in consultation with PI and colleagues; analyzing clinical data, conducting valid statistical tests and statistical models; and assisting with data visualization and communicating findings in presentations and manuscripts., • Specific tasks will include: database management, data extraction, data cleaning/quality checks, and conducting statistical analysis using linked and/or multiple data sources., • Focused tasks including, but not limited to, data cleaning, data harmonization, data quality control, and data analysis and interpretation (e.g. multivariate regression analyses, survival analyses, etc.)., • High School Diploma/GED required., • Bachelor's degree in a relevant field (e.g., life sciences, health sciences) preferred. License/Certification Requirements: • Certification in Clinical Research, ACRP/SoCRA (or equivalent) is required. Experience: • Five (5) years minimum experience in related field.

• CEDARS-SINAI

  

  Clinical Research Associate I - Urology

  4 days ago

  Los Angeles

  Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. With a team focused on effective pain management and quick recovery, Cedars-Sinai has been ranked as the No. 1 hospital in Southern California for Orthopaedics by U.S. News & World Report. Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements! The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. The CRAI evaluates and abstracts research data and ensures compliance with protocol and research objectives. This role is responsible for completing case report forms (CRFs) and entering clinical research data, as well as providing limited contact with research participants as needed for study and assists with study/long term follow-up research participants only. Primary Duties & Responsibilities: • Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study., • Evaluates and abstracts clinical research data from source documents., • Ensures compliance with protocol and overall clinical research objectives., • Completes Case Report Forms (CRFs)., • Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors., • Provides supervised patient contact or patient contact for long term follow-up patients only., • Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines., • Assists with clinical trial budgets., • Assists with patient research billing., • Schedules patients for research visits and research procedures., • Responsible for sample preparation and shipping and maintenance of study supplies and kits., • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board., • Maintains research practices using Good Clinical Practice (GCP) guidelines., • Maintains strict patient confidentiality according to HIPAA regulations and applicable law., • Participates in required training and education programs Qualifications Educational Requirements: High School Diploma/GED Bachelors degree in science or related degree preferred Experience: 1-year clinical research related experience preferred Physical Demands: Able to perform moderate lifting. Able to sit, stand and walk for prolonged periods of time. Able to read papers and online documents. Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions. Understanding of general clinical research objectives. Clinical research experience, preferred Req ID : 13483 Working Title : Clinical Research Associate I - Urology Department : Urology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $19.50 - $32.86