Senior Clinical Research Coordinator-Biorepository and Core Research Laboratory Ochsner Clinic FoundationSenior Clinical Research Coordinator-Biorepository and Core Research LaboratoryNew Orleans, LouisianaRemoteEven 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).
NewClinical Research Coordinator III Tulane UniversityClinical Research Coordinator IIILaFayette, LAPreferred Qualification: Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired. The Clinical Research Coordinator III screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive tests according to study protocols.
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.
NewSenior 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).
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.
Clinical Research Coordinator Ochsner Clinic FoundationClinical Research CoordinatorNew Orleans, LouisianaRemoteEven 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. Because the incumbent works within a healthcare setting, there may be occupational risk for exposure to hazardous medications or hazardous waste within the environment through receipt, transport, storage, preparation, dispensing, administration, cleaning and/or disposal of contaminated waste.
Clinical Research Coordinator - On Site Ochsner Clinic FoundationClinical Research Coordinator - On SiteNew Orleans, LouisianaRemoteEven 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, Maine, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington, and Washington D.C.
Clinical Research Coordinator 1 Louisiana State University Health Sciences Center New OrleansClinical Research Coordinator 1New Orleans, LAThis position offers an exciting opportunity to collaborate with leading investigators, clinicians, and academic staff to promote research excellence and improve patient outcomes through participation in cutting-edge clinical trials. 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 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 Research Coordinator IQVIA Holdings IncClinical Research CoordinatorKenner, LA$37,800–$94,500 / yearJoin 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 Research Coordinator No-Resistance Consulting GroupClinical Research CoordinatorBaton Rouge, LA$22.50–$25 / hourFull timeJob Location:Baton Rouge Expected Start Date: OctoberCompany Description:Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.
Clinical Research Coordinator (32211) GI AllianceClinical Research Coordinator (32211)Lafayette, LAWork directly with patients to screen, consent, take history, complete necessary exams including EKG, blood draw, vitals, etc. Research Coordinator 06.2020 • Assist with recruitment of studies, budget evaluation and negotiation, protocol evaluation, communication with study sponsors.
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.
RN Clinical Research Ochsner Clinic FoundationRN Clinical ResearchNew Orleans, LouisianaEven 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.
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. 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.
CLINICAL TRIALS COORDINATOR 1 or 2 Louisiana State University Health Sciences Center New OrleansCLINICAL TRIALS COORDINATOR 1 or 2New Orleans, LAOther 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.
CLINICAL TRIALS COORDINATOR 1, 2, or 3 Louisiana State University Health Sciences Center New OrleansCLINICAL TRIALS COORDINATOR 1, 2, or 3New Orleans, LAIncumbent must be comfortable working independently, managing interactions with and between team members, both internally and externally; ensuring that all NIH grant funded, industry-sponsored or investigator-driven studies/trials are managed to the highest quality to ensure safety and effectiveness. 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.
Research Compliance Coordinator III Tulane UniversityResearch Compliance Coordinator IIINew Orleans, LAAssists with the coordination of post-Approval Activities: Compose and distribute correspondence to investigators on behalf of the Board, Director, and/or Chairs; Prepare approval documentation in compliance with federal regulations, sponsor-related requirements, state and/or local law, and university policy; Compose clear, concise and detailed correspondence to investigators to ensure that the concerns, rationale, and technical questions of the IRB are quickly and intelligibly communicated to the researchers. Pre-Review IRB Submissions and Database Management: Pre-review protocols for completeness and compliance with regulations and IRB policies; Conducts evaluation of investigator's response to identify potential issues for IRB reviewers; Assigns the appropriate category under federal under federal guidelines and forwards the protocol to a board member for expedited review - or recommend that it be reviewed by the convened IRB; Determines the most expeditious processing mechanism allowed for an application based on an understanding of the proposed research and an interpretation of appropriate guidelines.
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.
Counselor/Coordinator of Clinical Programming Louisiana Tech UniversityCounselor/Coordinator of Clinical ProgrammingRuston, LAThe Counselor/Coordinator of Clinical Programming must be able to provide effective clinical services to students presenting with a range of mental health concerns; assess and respond appropriately to crisis situations; facilitate individual, couples, and group interventions; develop and coordinate clinical programs; communicate effectively with diverse university constituencies; utilize technology to enhance services; organize and manage multiple clinical and programmatic responsibilities; and participate in after-hours crisis response and presentations as required. The Counselor/Coordinator of Clinical Programming provides direct counseling, crisis intervention, assessment, consultation, and referral services to university students while developing and coordinating clinical programs that address identified student mental health needs.