NewClinical Director - Nursing Leadership CHRISTUS HealthClinical Director - Nursing LeadershipShreveport, LAImplementing and monitoring programs and practices for the delivery of safe and efficient quality nursing care for patients and their families. Resolves conflicts in a wide variety of situations, such as workload allocation, schedule overlap etc.
NewClinical Director - Telemetry / Nursing Leadership CHRISTUS HealthClinical Director - Telemetry / Nursing LeadershipAlexandria, LAImplementing and monitoring programs and practices for the delivery of safe and efficient quality nursing care for patients and their families. Master's degree in Nursing, Health Administration, Business Administration, Nursing, or related advanced degree in health health-related field preferred.
Clinical Care Manager, RN VitalCaring GroupClinical Care Manager, RNHammond, LAThis is a role for a strong clinician who thrives in ownership, collaboration, and a fast-paced environment - someone who can connect the dots across patients, providers, and teams to deliver exceptional outcomes. As a Clinical Care Manager (RN), you are at the center of that impact - leading coordination of care, guiding clinical decisions, and ensuring every patient receives the quality and attention they deserve.
Clinical Director UnitedHealth GroupClinical DirectorLafayette, LA$67,392–$101,088 / yearThis includes: coordinating and completing assigned projects to effectively support the immediate and long range objectives of the company; oversight of the eligibility of patients referred to home care services, planning for the services to be provided to patients and supervising their total home health care; implementing and maintaining administrative practices, agency philosophy, goals, and policies which assure compliance with applicable state and federal regulations; enhancing the profitability of the agency; and providing motivation and retention of a qualified staff and assure the quality of services delivered. As members of the Optum family of businesses, we are dedicated to helping people feel their best, including our team members who create meaningful connections with patients, their families, each other and the communities we serve.
Registered Nurse Clinical Educator Lead - Clinical Education Christus HealthRegistered Nurse Clinical Educator Lead - Clinical EducationAlexandria, LAThis role leads the design, implementation, and evaluation of high-impact education programs leveraging adult learning principles and advanced & innovative modalities such as simulation, digital, blended, and microlearning. The Lead Registered Nurse Clinical Educator serves as a key mentor and strategic resource within the nursing education team, advancing clinical excellence and supporting ministry and systemwide learning initiatives.
Clinical Account Executive-Home Health UnitedHealth GroupClinical Account Executive-Home HealthBaton Rouge, LA$72,048–$108,072 / yearAs members of the Optum family of businesses, we are dedicated to helping people feel their best, including our team members who create meaningful connections with patients, their families, each other and the communities we serve. See United Healthcare Privacy Policy at https://www.unitedhealthgroup.com/privacy.html and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.
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.
Clinical Research Assistant - OLOL FMOL HealthClinical Research Assistant - OLOLBaton Rouge, LAUnder the direct supervision of the Clinical Research Manager and the Principal Investigator (PI), the Research Assistant is responsible for the coordination and implementation of assigned research projects, data management, and communication of protocol activity within the Office of Research. Collaborates with PI and Clinical Research Manager to develop materials and tools necessary to appropriately train key personnel in the protocol requirements, schedule of visits, and execution of clinical trial agreement.
Clinical Research Coordinator III Tulane UniversityClinical Research Coordinator IIINew Orleans, LAThe Clinical Research Coordinator III screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects. 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.
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.
Director of Clinical Operations Louisiana State UniversityDirector of Clinical OperationsBaton Rouge, LAWorking closely with investigators, research teams, clinical partners, sponsors, and institutional leadership, the Director ensures research programs are effectively supported and positioned for success. The ideal candidate is an experienced clinical research or healthcare operations leader with a demonstrated ability to build high-performing teams, manage complex operations, and foster a culture of accountability, innovation, and continuous improvement.
Director Of Clinical Operations Louisiana State UniversityDirector Of Clinical OperationsBaton Rouge, LAWorking closely with investigators, research teams, clinical partners, sponsors, and institutional leadership, the Director ensures research programs are effectively supported and positioned for success. The ideal candidate is an experienced clinical research or healthcare operations leader with a demonstrated ability to build high-performing teams, manage complex operations, and foster a culture of accountability, innovation, and continuous improvement.
Clinical Research Nurse II Tulane UniversityClinical Research Nurse IINew Orleans, LAPreferred Qualification: Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP), National Board of Medical Examiners, OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired. The Research Nurse II can screen, enroll, and follow study patients, under the supervision, ensuring protocol compliance and close patient monitoring, continuing the required learning process required in this second level position for advancement toward a Research Nurse III position.
NewClinical Research Coordinator IQVIAClinical Research CoordinatorCovington, LouisianaJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits.
Clinical Documentation Registered Nurse - Clinical Documentation Integrity CHRISTUS HealthClinical Documentation Registered Nurse - Clinical Documentation IntegrityAlexandria, LAThe Clinical Documentation Registered Nurse collaborates extensively with physicians, nursing staff, other patient caregivers and coding staff to improve the quality and completeness of documentation of care provided and coded for coordination, abstraction and submission of accurate data required by CMS. Coordinates with quality department by: providing concurrent review for core measures documentation, providing retrospective chart audits as needed, and educating nursing and medical staff of improvement and current status of quality initiates.
Clinical Research Nurse RN Pediatric Oncology FMOL HealthClinical Research Nurse RN Pediatric OncologyBaton Rouge, LAThe Clinical Research Nurse - RN, under the guidance and supervision of the Principal Investigator (PI), ensures that the integrity and quality of clinical trials are maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals and FMOLHS policies and procedures. The research nurse will coordinate, manage, and assist physicians in enrolling, assessing and monitoring patients on Industry-Sponsored, NCI-Sponsored and/or Investigator Initiated clinical trials offered.
Clinical Research Coordinator Flourish ResearchClinical Research CoordinatorMandeville, LAFlourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
Clinical Director/Clinical Assistant Professor of MAP McNeese State UniversityClinical Director/Clinical Assistant Professor of MAPLake Charles, LALouisiana Revised Statute 42:31-Eligibility requirements for certain unclassified employees-requires any person hired or employed in an unclassified position, whose annual salary or rate of compensation is equal to or exceeds one hundred thousand dollars, provide proof to his public employer that he has been issued a Louisiana drivers license and that all vehicles registered in his name are registered in Louisiana within thirty days of being hired or employed at such salary. The Immigration Reform and Control Act of 1986 requires McNeese State University to inform applicants that the University can employ only U.S. citizens and aliens lawfully authorized to work in the U.S. Each new employee is required to present documentation verifying his/her identity and right to accept employment.
NewClinical Research Coordinator (Full-time; Days) - East Jefferson General Hospital Louisiana Childrens Medical Center IncClinical Research Coordinator (Full-time; Days) - East Jefferson General HospitalMetairie, 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. If you love science and a good checklist, can keep a dozen details moving without losing track of one, and want your work to contribute to the future of healthcare, this could be the role for you.
Senior Clinical Research Associate - Metabolic - Central Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Metabolic - CentralLA$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.