Senior Clinical Research Coordinator Tulane UniversitySenior Clinical Research CoordinatorNew Orleans, LAThe Senior Clinical Research Coordinator trains other staff in conducting, and may also perform as needed, simple procedures (vital signs, etc.) as called for by the study protocol(s).The Senior Clinical Research Coordinator serves as a key management and administrative role for the research project by supervising Clinical Research staff to ensure compliance with protocol, federal, and institutional requirements, and by frequently travelling to clinics to conduct trainings and site visits. The Senior Clinical Research Coordinator performs and supervises patient recruitment, enrollment, and follow-up, data collection, entry, and quality control activities, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects.
Clinical Research Coordinator I Tulane UniversityClinical Research Coordinator INew Orleans, LALegally protected demographic classifications (such as a person's race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane's employment or educational programs or activities. The Clinical Research Coordinator screens, enrolls and follows study patients, ensuring protocol compliance, and effective monitoring of clinical trial subjects.
Clinical Research Coordinator II Tulane UniversityClinical Research Coordinator IINew Orleans, LAFlexibility to work evenings and weekends, as needed, and to be available to respond promptly to all communications from study participants, trial clinical research coordinators, and clinic staff on for emergency situations or answer questions. Proven ability to oversee day-to-day operations of clinical trials including their respective regulatory and administrative processes including informed consent, eligibility review, protocol implementation, IRB approval, DSMP, and event reporting.
Senior Clinical Research Coordinator Ochsner Health SystemSenior Clinical Research CoordinatorNew Orleans, LARemoteEven though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. Evaluates competing strategies for recruiting study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings and coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials, serving as a liaison for both patient and Principal Investigator (PI).
Clinical Research Coordinator I Care AccessClinical Research Coordinator IShreveport, LA$55,000–$85,000 / yearp>With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Certifications/Licenses, Education, and Experience:Bachelor's Degree preferred, or equivalent combination of education, training, and experience.
Clinical Research Coordinator LSU Health ShreveportClinical Research CoordinatorShreveport, LASpecific duties include patient recruitment and assessment of patient eligibility, enrollment in appropriate trials, implementation of treatment or other research plans according to protocol guidelines, case management of protocol subjects, management of study drug supplies and drug accountability, education of other healthcare professionals, patients, and families regarding clinical trial participation, timely and accurate collection and submission of research data to clinical trial sponsors, completion of long-term follow-up of study patients, chart preparation for and participation in all quality assurance, FDA, and NCI audits, timely maintenance of in-house patient management database, completion of study queries, compilation, analysis and verification of statistics, initiation of and response to correspondence related to research activities, assistance with training additional affiliate sites in the conduct of clinical trials. Identify which study drugs are supplied by the study, order drugs in a timely manner in order to ensure that patients are treated with study-supplied drugs, and alert research pharmacist when such drugs are being ordered for a study.
associate clinical research coordinator Ochsner Health Systemassociate clinical research coordinatorNew Orleans, LARemoteEven though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. Individuals who reside in and will work from the following areas are not eligible for remote work position: Colorado, California, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington, and Washington D.C. Ochsner Health endeavors to make our site accessible to all users.
Clinical Research Coordinator - Baton Rouge Ochsner Health SystemClinical Research Coordinator - Baton RougeBaton Rouge, LARemoteEven though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. Individuals who reside in and will work from the following areas are not eligible for remote work position: Colorado, California, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington, and Washington D.C. Ochsner Health endeavors to make our site accessible to all users.
Clinical Research Coordinator DelRicht ResearchClinical Research CoordinatorRiver Ridge, LAp>Overall, the Clinical Research Coordinator is responsible for supporting high-quality study execution and helping expand site capacity in a busy clinical research environment: Patients are welcomed into a professional, supportive, and efficient clinic environment throughout their study participation. DelRicht Research has been recognized as a Top Workplace for 2023, 2024, and 2025! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.
Clinical Research Coordinator (31267) GI AllianceClinical Research Coordinator (31267)Lafayette, LAActs as an experienced resource for Clinical Research Coordinators I and Research Assistants during new hire training, newly initiated trials, and trial transitions. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions: Physical demands: Involves sitting approximately 90 percent of the day, walking or standing for the remainder.
Clinical Research Coordinator I Care Access Research LLCClinical Research Coordinator IShreveport, LA$55,000–$85,000 / yearp>With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Sr Clinical Research Coord Ochsner Health SystemSr Clinical Research CoordNew Orleans, LARemoteEven though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. Evaluates competing strategies for recruiting study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings and coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials, serving as a liaison for both patient and Principal Investigator (PI).
Senior Research Compliance Coordinator Tulane UniversitySenior Research Compliance CoordinatorNew Orleans, LAli>Two years of experience and knowledge related to IRB matters and human subjects research protection or equivalent combination of experience and education (typical experience might include ethics, clinical trial performance, industry, and/or experience in an academic health center or medical school); Experience with reviewing local and/or state laws and federal regulations (i.e. 45 CFR 46, 21 CFR 50,56, HIPAA, Good Clinical Practice, the Declaration of Helsinki, and the Belmont Report), and local IRB policies regarding human subjects research; or ability to learn these regulations; Experience in Windows-based applications. Working knowledge of the Belmont Report, the Declaration of Helsinki, and the Nuremberg Code; Understand the operation of the Food and Drug Administration (FDA) and the Federal Office of Human Research Protections (OHRP); Demonstrates administrative skills; and must be motivated and able to work in a high volume office; Excellent written and oral communications skills; excellent customer service skills; and must possess a high level of interpersonal skills; Highly organized and detail-oriented.
Research Coordinator - Full-Time Woman's HospitalResearch Coordinator - Full-TimeBaton Rouge, LA$20.82–$30.19 / hourStudy coordination: study visit preparation and implementation (including but not limited to: patient education for research protocols, obtaining informed consent from research participants, reconsenting participants, registering/ordering clinical, imaging, and laboratory tests; visit scheduling; data collection; accurately assessing patients to determine their preliminary or complete eligibility for research protocols; chart setup and processing); Maintains data collection on research participants; maintains accurate and complete documentation; assists in specimen handling and distribution of medicine as directed for research subjects and clinical tests. Responsibilities include managing and coordinating clinical trial studies, handling data management, obtaining participant consent, communicating study status, and collaborating with other coordinators, nurses, dietitians, Principal Investigators, and ancillary departments.
GME Research Coordinator Willis Knighton Medical CenterGME Research CoordinatorShreveport, LAQUALIFICATIONS: EDUCATION EXPERIENCE Prefer a bachelors degree in a science-related field or masters degree with a focus in data analytics Prefer experience in research and/ or clinical trials Prefer experience in coordination Prefer experience with humanresearch protections CITI Certification in Good Clinical Practice (GCP) or completed within first month of employment CRA (CITI) Certification or completed within first month of employment. The Department of Graduate Medical Education Research at Willis Knighton Health is seeking a qualified research coordinator to assist with the planning, execution, and management of scholarly activities being performed by residents, fellows, medical students, and other potential student categories at Willis Knighton Health.
Coordinator Research - Research Industry CHRISTUS HealthCoordinator Research - Research IndustryAlexandria, LAThis position will market CHRISTUS research services, create and maintain research activity databases, and monitor the impacts of the research studies to include financial and safety risks. Maintain and continually refine customized, networked computerized database to allow for timely tracking of research projects scheduled for re-review.
RN CLINICAL TRIALS COORDINATOR 2 Louisiana State University Health Sciences Center New OrleansRN CLINICAL TRIALS COORDINATOR 2New Orleans, LADuties will include: attending oncology clinics in-person and virtually to collaborate with physicians to determine patient eligibility; informing and educating the patient and their families about a particular study; providing informed consent; scheduling regular appointments and follow-up as needed; providing treatment; obtaining study specific lab-work; evaluating and monitoring effects of treatment; organizing, collecting and managing data; submitting forms and reports as required; working closely with monitors from the drug companies to ensure protocols are being implemented correctly and that the necessary clinical data is being captured; processing and packaging specimens for mail-out. The RN CTC2 will recruit, enroll, administer care, and provide patient follow-up visits in-person and virtually on all NCI and pharmaceutical sponsored studies associated with the Cancer Center, the Genitourinary Oncology team, Gynecologic Oncology team, and its partner institutions.
NewResearch Coordinator - Cord Blood Collection Program Woman's HospitalResearch Coordinator - Cord Blood Collection ProgramBaton Rouge, LA$20.82–$30.19 / hourp>The cord blood collector is responsible for identifying potential cord blood donors prior to delivery; educating, interviewing, and consenting potential donors; collecting or assisting with the in-utero cord blood collection at delivery; conducting ex-utero cord blood collection; and preparing collected cord blood and maternal blood samples with associated documentation for shipping. In fact, for the 17th year in a row, Woman's has been recognized as a Best Place to Work by Modern Healthcare - making us the only healthcare organization to earn the distinction every year since the program's inception.
Per Diem Clin Research Coordinator II - Onsite in West Monroe, Louisiana Syneos HealthPer Diem Clin Research Coordinator II - Onsite in West Monroe, LouisianaLouisianaPer Diem Clin Research Coordinator II - Onsite in West Monroe, LouisianaIllingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.
Per Diem Clin Research Coordinator II - Onsite Lafayette, Louisiana Syneos HealthPer Diem Clin Research Coordinator II - Onsite Lafayette, LouisianaLouisianadiv>Per Diem Clin Research Coordinator II - Onsite Lafayette, LouisianaIllingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.
CLINICAL TRIALS COORDINATOR 1, 2 or 3 Louisiana State University Health Sciences Center New OrleansCLINICAL TRIALS COORDINATOR 1, 2 or 3New Orleans, LANumber of years required to perform the job: Clinical Trials Coordinator 1: 1 year; Clinical Trials Coordinator 2: 3 years; Clinical Trials Coordinator 3: 5 years. Comprehensive benefits are available to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement plans; generous annual and sick leave; 14 paid holidays per year; and an employee health primary care clinic.
CLINICAL TRIALS COORDINATOR 1 or 2 Louisiana State University Health Sciences Center New OrleansCLINICAL TRIALS COORDINATOR 1 or 2New Orleans, LAp>Other employee benefits include a full-service credit union, wellness benefits featuring complimentary fitness center membership for employees and their spouses, employee assistance program, campus assistance program, and pet insurance option. Comprehensive benefits are available to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement plans; generous annual and sick leave; 14 paid holidays per year; and an employee health primary care clinic.
Per Diem Clin Research Coordinator II - Onsite in West Monroe, Louisiana Syneos Health IncPer Diem Clin Research Coordinator II - Onsite in West Monroe, LouisianaWest Monroe, LATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Per Diem Clin Research Coordinator II - Onsite Lafayette, Louisiana Syneos Health IncPer Diem Clin Research Coordinator II - Onsite Lafayette, LouisianaLafayette, LATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Research Nurse - Clinical Trials Outpatient Unit Louisiana State UniversityResearch Nurse - Clinical Trials Outpatient UnitBaton Rouge, LAProvide individualized education and counseling to research participants regarding study procedures, investigational treatments, medication administration, potential side effects, and the importance of protocol adherence, fostering participant engagement and trust throughout the clinical trial experience. Administer investigational medications and injectable study products in accordance with study protocols, institutional policies, and regulatory requirements while closely monitoring participants for adverse reactions and documenting all activities accurately and thoroughly.
NURSING FACULTY (OPEN RANK)-COORDINATOR CLINICAL SPECIALIST Louisiana State University Health Sciences Center New OrleansNURSING FACULTY (OPEN RANK)-COORDINATOR CLINICAL SPECIALISTNew Orleans, LAOur nursing faculty have the opportunity to educate future nurses at the BSN, MN/MSN, PhD and DNP level, including state-of-the-art simulation laboratories; conduct nursing & interdisciplinary research; engage in faculty practice, including our nurse-run clinics; pursue entrepreneurial and consultative activities; and serve as a nursing leader and development of leadership skills through our Emergent Nurse Leader Program. Comprehensive benefits are available to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement plans; generous annual and sick leave; 14 paid holidays per year; and an employee health primary care clinic.
Senior Clinical Project Manager Tulane UniversitySenior Clinical Project ManagerNew Orleans, LAIn addition, the Clinical research Project Manager will support the development of research projects including proposal applications, scientific study design, IRB protocols, budgets, contracts, personnel recruitment, hiring, and training, as well as reports on expenses, progress, and effort in collaboration with the Associate Director. In addition, this person will serve in a key management and administrative role for all clinical research projects conducted at the TRIAD Center through the management of the clinical research team and ensuring compliance with established protocols, study timelines as well as institutional, local, and federal requirements.
Research Regulatory Specialist Senior Louisiana Childrens Medical Center IncResearch Regulatory Specialist SeniorNew Orleans, LAUniversity Medical Center, a world class academic medical center in LCMC Health's incredible community of care, is the largest medical training center for healthcare professionals in Louisiana and has long served as the region's safety net hospital for poor and underserved communities for 300+. While our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way.
Research Nuclear Medicine Technologist Louisiana Childrens Medical Center IncResearch Nuclear Medicine TechnologistMetairie, LAWhile our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way. East Jefferson General Hospital, a landmark of LCMC Health's incredible community of care, has been the go-to hospital for health, wellness, and one-of-a-kind care in East Jefferson Parish for over 50 years.
Student Research Aide 1 - Epidemiology Tulane UniversityStudent Research Aide 1 - EpidemiologyNew Orleans, LAQualified and interested assistants will support Lab Technician and Clinical Research Coordinators in lab tasks, including the collecting, processing, and storing of biological samples. Legally protected demographic classifications (such as a person's race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane's employment or educational programs or activities.
RN Clinical Researcher Ochsner Health SystemRN Clinical ResearcherNew Orleans, LAEven though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials, serving as a liaison for both patient and the private investigator (PI) and monitors patients for safety and adverse events during medical procedures, including administration of parenteral investigational agents depending on area of assignment.
NewPatient Data Coordinator DelRicht ResearchPatient Data CoordinatorMetairie, LA$20–$22.50 / hourThe Patient Data Coordinator will maintain all activities related to the accurate and timely handling of clinical research data including but not limited to: Enter, review, and reconcile clinical research data with a strong focus on accuracy and completeness. Patient Data Coordinator's Main Objective: The Patient Data Coordinator will assist our centralized team with providing high level support organizing and completing the day-to-day data entry and data quality activities that support our clinical research sites.
Healthcare Project Coordinator DelRicht ResearchHealthcare Project CoordinatorRiver Ridge, LAp>Overall, the Healthcare Project Coordinator is responsible for supporting efficient, accurate, and organized study start-up operations for clinical trials across DelRicht Research: Patients are welcomed into a professional, supportive, and efficient clinic environment throughout their study participation. Required: Strong organization, communication, and time management skills in healthcare, clinical research, project coordination, administrative operations, vendor coordination, or systems-related work.
Manager - Research Finance Ochsner Health SystemManager - Research FinanceNew Orleans, LAIndividuals who reside in and will work from the following areas are not eligible for remote work position: Colorado, California, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington, and Washington D.C. Ochsner Health endeavors to make our site accessible to all users. Required - Certification from a relevant accredited research institution/professional organization such as the Association of Clinical Research Professionals (ACRP), Society of Clinical Research Associates (SOCRA), or International Society for Biological and Environmental Repositories (ISBER) within 1 year of hire.
Coordinator - Fiscal Operations Louisiana State UniversityCoordinator - Fiscal OperationsBaton Rouge, LACoordinate and maintain monthly telecommunications billing processes, including teleconferencing services, cellular accounts, data services, and other communication-related operational expenses, ensuring accurate allocation, reconciliation, and timely processing. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities.
COMD Office Support Coordinator Louisiana State UniversityCOMD Office Support CoordinatorBaton Rouge, LAp>Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Benefits - LSU offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!
Clinical Lead Specialist, Structural Heart, TAVI (Dallas, Houston, New Orleans) Abbott LaboratoriesClinical Lead Specialist, Structural Heart, TAVI (Dallas, Houston, New Orleans)New Orleans, LA$78,000–$156,000 / yearTrain the trainer activities as an extension supporting field training needs to include proctoring, case observation host, solo case authorization, boot camp support and assisting with field mentoring of new hires from time of hire to solo case support. • Communicating product, clinical and market data to appropriate personnel inform customers of the latest product, therapy and technology developments in the industry and engages in clinical, procedural, and technical discussions, and link data outcome to key messaging.
Trauma Registry Coordinator (Trauma Data Abstractor) Louisiana Childrens Medical Center IncTrauma Registry Coordinator (Trauma Data Abstractor)New Orleans, LARemoteWorks with Patients, Families and Staff: Establishes working relationships with members of the hospital community including staff in various departments whose support is necessary for the management and success of the program. NTDB/TQIP Participation: Completes the American Trauma Societys Trauma Registrar Course, AAAM Injury Scaling Course and the Trauma registry specific continuing education as required.
NewSupply Coordinator 2 FMOL HealthSupply Coordinator 2Monroe, LAli>Identifies changes in supply usage and initiates change in stock on hand levels; ensures appropriate label changes are completed to reflect accurate information; enters all system changes to local item master files. Because of our size and the partnerships we have with other local organizations, we are able to pool our resources and share cost and service efficiencies and learn from each other, thereby accelerating our ability to improve care and solve challenges.
DEPARTMENT COORDINATOR Louisiana State University Health Sciences Center New OrleansDEPARTMENT COORDINATORNew Orleans, LAThe SAHP provides multidisciplinary outpatient services to achieve diversity of patient objectives that include diagnostic, therapeutic, and restorative services to enable patients to achieve as much functional, social, and occupational independence as is reasonably possible. This position supports the administrative and operational needs of the Dean, Associate Dean of Academic Affairs, Associate Dean of Student Affairs, Assistant Dean of Alumni & Community Affairs and other leadership as directed by the Assistant to the Dean.
CLINIC OPERATIONS COORDINATOR Louisiana State University Health Sciences Center New OrleansCLINIC OPERATIONS COORDINATORNew Orleans, LAThe SAHP provides multidisciplinary outpatient services to achieve diversity of patient objectives that include diagnostic, therapeutic, and restorative services to enable patients to achieve as much functional, social, and occupational independence as is reasonably possible. The School of Allied Health Professions is committed to providing quality education, leadership, research, and public service through direct patient care and community outreach by clinical healthcare professionals.
Registered Nurse Supervisor-Operations Coordinator Ochsner HealthRegistered Nurse Supervisor-Operations CoordinatorCrowley, LouisianaOchsner Health is seeking an experienced Registered Nurse (RN) to join our leadership team as a Supervisor – RN Operations Coordinator on the Medical‑Surgical (Med‑Surg) unit at Ochsner Acadia General Hospital in Crowley, Louisiana. Ochsner Health healed more than 876,000 people from across the globe in 2019, providing the latest medical breakthroughs and therapies, including digital medicine for chronic conditions and telehealth specialty services.
Data Coordinator III Tulane UniversityData Coordinator IIINew Orleans, LAAssists in the collection, management, and analysis of clinical and research data for the Pediatric Hematology/Oncology Program at Tulane University, including initiatives related to the Sickle Cell Center of Southern Louisiana and the Hematology/Oncology service line at Manning Family Children's Hospital. Legally protected demographic classifications (such as a person's race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane's employment or educational programs or activities.
NURSING FACULTY (OPEN RANK)-COORDINATOR OF NEONATAL NURSE PRACTITIONER CONCENTRATION Louisiana State University Health Sciences Center New OrleansNURSING FACULTY (OPEN RANK)-COORDINATOR OF NEONATAL NURSE PRACTITIONER CONCENTRATIONNew Orleans, LAOur nursing faculty have the opportunity to educate future nurses at the BSN, MN/MSN, PhD and DNP level, including state-of-the-art simulation laboratories; conduct nursing & interdisciplinary research; engage in faculty practice, including our nurse-run clinics; pursue entrepreneurial and consultative activities; and serve as a nursing leader and development of leadership skills through our Emergent Nurse Leader Program. Preferred Experience: Recent clinical practice as an NNP; Prior experience in teaching at the graduate nursing level; Prior experience with graduate program administration; Prior experience guiding DNP scholarly projects or doctoral dissertations.
UNDERGRADUATE MEDICAL EDUCATION COORDINATOR-REVISED Louisiana State University Health Sciences Center New OrleansUNDERGRADUATE MEDICAL EDUCATION COORDINATOR-REVISEDNew Orleans, LAUnder the supervision of the Associate Dean for Undergraduate Medical Education (UME) and the Manager of Undergraduate Medical Education, the incumbent will provide administrative and operational support to the Office of UME and assist the Directors of Clinical Sciences and Basic Sciences Curriculum as needed to deliver the medical curriculum. This role provides comprehensive administrative and technical support for Level 1 medical education courses and longitudinal honors tracks, ensuring smooth delivery of curriculum, assessments, and student learning activities.
UME DEPARTMENT COORDINATOR Louisiana State University Health Sciences Center New OrleansUME DEPARTMENT COORDINATORNew Orleans, LAUnder the supervision of the Associate Dean for Undergraduate Medical Education (UME) and the Manager of Undergraduate Medical Education, the incumbent will provide administrative and operational support to the Office of UME and assist the Directors of Clinical Sciences and Basic Sciences Curriculum as needed to deliver the medical curriculum. The medical education program prepares students to become physicians who consistently display attributes befitting to the profession of medicine and who engage in continuous learning for the benefit of their patients.
Clinical Behavior Analyst McNeese State UniversityClinical Behavior AnalystLake Charles, LACollaboration & Communication: • Assist in identification, selection, training, supervision and evaluation of line technicians, graduate assistants, and interns as assigned by the Clinical Director • Provide input to clinical staff and faculty in assessing degree curriculum content and competencies of degree-seeking students progressing through graduate program in psychology/applied behavior analysis • Collaborate with both faculty and the Clinical Director to develop remediation plans for students not meeting acceptable progress benchmarks as outlined in the Student Handbook • Collaborate with others by serving on committees, task forces, research teams and related work groups appropriate to role within department, college, university, community, and profession • Work to establish MAPs reputation as a premier university-based training site for students in ABA • Provide leadership in managing special projects and tasks within department as needed or requested. • Supervision & Training: • Provides supervision to Graduate/Undergraduate-Level Student Employees and ABA interns in accordance with BACB requirements • RLTs/WAE-Contract Employees • Support interns in developing clinical, professional, and ethical competencies • Model effective ABA strategies and professional behavior • Participate in training meetings, case reviews, and professional development activities • Collaborate with senior BCBA to ensure quality supervision and intern success • Document intern supervision in accordance with the BACB guidelines.
Hospital Supply Coordinator Louisiana State UniversityHospital Supply CoordinatorLAp>Vehicle Operation -University employees whose principal responsibilities of employment include operating a vehicle, performing maintenance on a vehicle, or supervising any public employee who operates or maintains a vehicle and positions with an expectation to travel will require an MVR and are subject to drug screens per PM-33/PS-67/FASOP HR-04. Safety and Security Sensitive Job - Safety and security-sensitive positions are defined as those positions where any form of substance abuse may affect University activities through unsafe work behavior/performance or error in judgment; or where substance abuse could jeopardize the safety and well-being of employees, other personnel, or the general public, or cause significant damage to University property.
LPN Intake Coordinator (Home Health) LHC Group IncLPN Intake Coordinator (Home Health)Harahan, LAWe strive to offer benefits that reward the whole you! employee wellness programs flexibility for true work-life balance holidays & paid time off continuing education & career growth opportunities company-wide support & resources to help you achieve your goals Take your career to a new level of caring. At Egan - Ochsner Home Health New Orleans, a part of LHC Group, we embrace a culture of caring, belonging, and trust and enjoy the meaningful connections that come from it: for the whole patient, their families, each other, and the communities we serve-it truly is all about helping people.
LPN Intake Coordinator LHC Group IncLPN Intake CoordinatorRaceland, LAWe strive to offer benefits that reward the whole you! employee wellness programs flexibility for true work-life balance holidays & paid time off continuing education & career growth opportunities company-wide support & resources to help you achieve your goals Take your career to a new level of caring. At Ochsner Home Health of Raceland, a part of LHC Group, we embrace a culture of caring, belonging, and trust and enjoy the meaningful connections that come from it: for the whole patient, their families, each other, and the communities we serve-it truly is all about helping people.