Med Surg Clinical Nurse Coordinator TriStar NorthCrest Medical CenterMed Surg Clinical Nurse CoordinatorSpringfield, TNIn collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
NewClinical Research Physician (POOLING) K2 Staffing LLCClinical Research Physician (POOLING)Berry Hill, TNAs a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. We have taken part in clinical trials for all current FDA-approved therapies that slow the progression of Alzheimer’s disease (AD) and most diagnostics (PET tracers, CSF and blood biomarkers) for the diagnosis of AD.
NewRespiratory Care Shift Coordinator FT Days Prisma HealthRespiratory Care Shift Coordinator FT DaysMaryville, TNMinimum Requirements Education - Associate degree in Respiratory Therapy or other related field and a graduate of a school of Respiratory Therapy approved by the American Medical Association or successor accrediting authority. Instructs, applies and mentors staff in advanced level technical skills, critical thinking and problem-solving strategies to intervene in complex patient care situations.
Admissions Coordinator Dialysis Clinic, Inc.Admissions CoordinatorNashville, TN$19–$22 / hourDCI’s Differentiator: Since opening the first clinic 50 years ago in Nashville, Tenn., our Dialysis Clinic, Inc. family has grown to be the nation’s largest nonprofit dialysis provider with more than 270 locations in 30 states, serving nearly 14,000 patients each day. The Regional Admissions Coordinator is responsible for duties related to admission of all end stage renal disease (ESRD) patients, permanent and transient, for the regional group of mid-TN clinics assigned.
staff - Registered Nurse (RN) - Med Surg - $38-42 per hour Perm Staff Jobsstaff - Registered Nurse (RN) - Med Surg - $38-42 per hourSpringfield, TN$38–$42 / hourIn collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
Clinical Research Coordinator HCA Healthcare IncClinical Research CoordinatorNashville, TNPerforms routine operational activities for multiple research protocols Liaise between site research personnel, industry sponsors, and Supervisor Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable Coordinates schedule of assessments from initial submission of feasibility until study closeout Reviews the study design and inclusion/exclusion criteria with physician and patient Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data Creates study specific tools for source documentation when not provided by sponsor Collects, completes, and enters data into study specific case report forms or electronic data capture systems Generates and tracks drug shipments, device shipments, and supplies as needed · Ensures timely and accurate data completion Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations Communicates all protocol-related issues to appropriate study personnel or manager Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required Reviews and responds to any monitoring and auditing findings Practice and adhere to the "Code of Conduct" philosophy and "Mission and Value Statement" Education/Experience: Bachelor's Degree or 1+ year of equivalent experience required Certifications: Certified Clinical Research Coordinator preferred Benefits TriStar Centennial Medical Center, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The Clinical Research Coordinator is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors.
Clinical Research Coordinator I OraClinical Research Coordinator INashville, TennesseePerform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I’s will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
Clinical Research Coordinator I Ora, Inc.Clinical Research Coordinator INashville, TNPerform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred West Cancer CenterClinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) PreferredGermantown, TNThe Clinical Research Coordinator plays a vital role in managing oncology patients participating in pharmaceutical-sponsored clinical trials. If you are a detail-oriented clinical research professional looking to make a difference in oncology care, apply today to become a Clinical Research Coordinator at West Cancer Center.
Clinical Research Coordinator II Care AccessClinical Research Coordinator IIMemphis, Tennessee$60,000–$90,000 / yearWith 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.
Clinical Research Coordinator 4 Vanderbilt University Medical CenterClinical Research Coordinator 4Nashville, TNAligning with Vanderbilt Health's Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
Clinical Research Coordinator III Vanderbilt HealthClinical Research Coordinator IIINashville, TNAligning with Vanderbilt Health's Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
Clinical Research Coordinator III Vanderbilt University Medical CenterClinical Research Coordinator IIINashville, TennesseeAligning with Vanderbilt Health’s Strategic Directions , the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
Research Study Coordinator 1-Research Center (Knoxville) University of Tennessee SystemResearch Study Coordinator 1-Research Center (Knoxville)Knoxville, TNAssists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication, obtaining informed consent, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies. This position assists the faculty with clinical research study activities including but not limited to the development, submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, and preparation and maintenance of study files and essential trial documents.
Research Coordinator I Erlanger HealthResearch Coordinator IChattanooga, TNRequired: Certification in Institution Review Board required Course in The Protection of human Research subjects (CITI) course in Protection in Human Research Subjects, Conflict of Interest and Good Clinical Practice; International Air Transportation Association (IATA) certification for shipping dangerous goods and biological substances. Ability to work in a typical office setting with some stressful situations, personal flexibility; moderate sitting, stooping, bending, and moderate work at word processing screen required.
Research Coordinator 1-Pediatrics University of Tennessee SystemResearch Coordinator 1-PediatricsMemphis, TNEXPERIENCE: One (1) year of research experience in subject recruitment, informed consent, understanding of IRB requirements, and following a research study protocol; OR a combination of education and experience to equal five (5) years. The Research Coordinator 1 recruits young children with a first acute respiratory virus infection (RSV, SARS-CoV-2, influenza) in the Emergency Department and inpatient floors at Le Bonheur.
Clinical Research Coordinator II Tennessee OncologyClinical Research Coordinator IIGallatin, TNEstablished 1976 in Nashville, Tennessee Oncology's mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. ESSENTIAL FUNCTIONS: Screens potential subjects for clinical trials through a careful review of the patient's past medical history and a review of current findings against inclusion and exclusion criteria specific to a trial.
Clinical Research Coordinator (31656) GI AllianceClinical Research Coordinator (31656)Germantown, TNWork with other research department staff in a leadership role including management, training, delegation of responsibilities, hiring, etc. Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal.
Clinical Research Coordinator Nurse II Meharry Medical CollegeClinical Research Coordinator Nurse IINashville, TennesseeResponsible for managing accounts receivable and accounts payable in clinical research; Assist with reviews, analyzes and negotiates all clinical research budgets and contracts with sponsors under the direction of the Principal Investigator/ Associate Director. Responds to inquiries on study projects, ensures compliance of protocols and overall objectives, and performs study-related procedures of clinical research under the supervision of the Principal Investigators.
Clinical Research Coordinator II Meharry Medical CollegeClinical Research Coordinator IINashville, TNResponsible for managing accounts receivable and accounts payable in clinical research; Assist with reviews, analyzes and negotiates all clinical research budgets and contracts with sponsors under the direction of the Principal Investigator/ Associate Director. Essential Functions (Duties and Responsibilities) - Assign a percentage to each essential function: Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses and travel to participant's location for recruitment activities.
Clinical Research Coordinator II Care Access Research LLCClinical Research Coordinator IIMemphis, TN$60,000–$90,000 / yearWith 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.
Coordinator-Research Nurse I RN Baptist Memorial Health CareCoordinator-Research Nurse I RNMemphis, TNThe Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up.
NewClinical Research Coordinator I Vanderbilt University Medical CenterClinical Research Coordinator INashville, TennesseeServes as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants. With direction, performs or instructs others in performing procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and in a timely manner reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine if a protocol amendment or other safety reporting to appropriate funding/regulatory agencies is required.
Coordinator-Research Nurse I RN Baptist Memorial Health Care CorpCoordinator-Research Nurse I RNMemphis, TNThe Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up.
Clinical Research Regulatory & Study Start-Up Coordinator 1827 Urology Associates, PCClinical Research Regulatory & Study Start-Up CoordinatorNashville, TNFull timeWorking in close collaboration with the Clinical Research Department Manager, Principal Investigators (PIs), Clinical Research Coordinators (CRCs), and external sponsors and Contract Research Organizations (CROs), the Regulatory & Study Start-Up Coordinator ensures that all regulatory submissions, essential document collections, IRB communications, and trial master file activities are executed with accuracy and in strict accordance with ICH E6(R2) Good Clinical Practice (GCP) guidelines, applicable FDA regulations (21 CFR Parts 50, 54, 56, and 312/812), and Urology Associates institutional SOPs. This role serves as the department's primary owner of site regulatory compliance and new study activation, ensuring that every clinical trial is initiated correctly, documented thoroughly, and maintained in a state of continuous inspection-readiness throughout its lifecycle.
Research Study Coordinator 2-Obstetrics and Gynecology University of Tennessee SystemResearch Study Coordinator 2-Obstetrics and GynecologyMemphis, TN$4,182.12–$5,000Creates and maintains study logs for effective trial management; maintains regulatory documents and study communications in the appropriate projects critical documents binder. JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Study Coordinator 2 plans, directs, and coordinates activities related to clinical research in the Department of Obstetrics & Gynecology.
NewSleep Tech Research Coordinator Vanderbilt University Medical CenterSleep Tech Research CoordinatorNashville, TennesseeServes as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants. Aligning with Vanderbilt Health’s Strategic Directions , the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.
Research Regulatory Coordinator Tennesssee OncologyResearch Regulatory CoordinatorNashville, TNEstablished 1976 in Nashville, Tennessee Oncology's mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Research Study Coordinator-Psychiatry University of Tennessee SystemResearch Study Coordinator-PsychiatryMemphis, TNJOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Study Coordinator 1 works with The Cowan Lab in the Department of Psychiatry on an institution-funded grant examining pain experience in individuals with substance misuse. Assists in gift card compensation, regulatory documentation, and other aspects of data collection, storage, and processing, per sponsor and site-specific protocols.
Research Coordinator - Oak Ridge Innovation Institute - UTK University of Tennessee SystemResearch Coordinator - Oak Ridge Innovation Institute - UTKKnoxville, TNRemoteProvide technical assistance to faculty, postdoctoral associates, and graduate students relative to all aspects of proposal support including dissemination of funding opportunities, analysis and interpretation of funding agency opportunities (e.g., solicitations, request for proposals, program guidelines), grants management system(s) support, proposal preparation timeline(s) and checklists, budget development, facilitation of internal/external collaborative arrangements, and proposal submission assistance to the funding agency. Coordinate the strategic development of large proposals (multi-year, multi-investigator projects in excess of $2 million/year); identify senior participants and research partners, both internal and external to the University (e.g., other universities, national laboratories, private industry).
NewRegional TCSEPP Coordinator: Social Work Research & Public Service - UTK University of Tennessee SystemRegional TCSEPP Coordinator: Social Work Research & Public Service - UTKKnoxville, TNOver the past fifty years, SWORPS has worked with local nonprofits such as the United Way of Greater Knoxville, University of Tennessee departments and faculty researchers, state agencies such as the Tennessee Department of Human Services, and federal agencies like the Department of Housing and Urban Development. Within SWORPS, the Tennessee Child Support Employment and Parenting Program (TCSEPP) Regional Coordinator builds a strong evidence-informed and trauma-informed practice that assists, supports, and advocates for non-custodial parents involved with the child support system.
Research Area Coordinator Vanderbilt UniversityResearch Area CoordinatorNashville, TNLocated in Nashville, Tennessee, on a 330+ acre campus and arboretum dating back to 1873, Vanderbilt is proud to have been named as one of "America's Best Large Employers" as well as a top employer in Tennessee and the Nashville metropolitan area by Forbes for several years running. Working closely with faculty, staff, and administrative partners across the College, the Coordinator supports meeting and event logistics, travel coordination, visitor support, communications, procurement, and other administrative activities.
Academic Medical Research Coordinator East Tennessee State UniversityAcademic Medical Research CoordinatorJohnson City, TNProvides advanced coordination and administrative research support for graduate medical education, residency/fellowship programs, and serves as a liaison for undergraduate students involved in medical research at Quillen College of Medicine. Plays a key role in ensuring that programs meet institutional and regulatory requirements related to research, often working independently and with increased accountability for compliance and program performance.
CIRCLE Research Project Coordinator - College of Education, Health and Human Sciences - UTK University of Tennessee SystemCIRCLE Research Project Coordinator - College of Education, Health and Human Sciences - UTKKnoxville, TNThis position coordinates and manages the implementation of research-focused initiatives and associated research programming between the University of Tennessee (UT) and River Valley Health (RVH [formerly Cherokee Health Systems]) for three CEHHS faculty members that are part of a cluster hire initiative to partner with RVH. The university holds the highest Carnegie classification for research activity and has deep partnerships with industry leaders and the US Department of Energy's largest multidisciplinary laboratory, Oak Ridge National Laboratory.
Commercialization Coordinator (Research & Innovation) Meharry Medical CollegeCommercialization Coordinator (Research & Innovation)Nashville, TennesseeThe ideal candidate is organized, proactive, and has great communication skills who can assist in helping support early-stage innovation in a university academic medical environment. The Commercialization Coordinator will collaborate closely with the Commercialization Counselor and help support innovation, entrepreneurship, and technology transfer activities across the institution.
Clinical Research Assistant (30795) GI AllianceClinical Research Assistant (30795)Germantown, TNResearch Assistants support the Clinical Research Team with subject recruitment, diagnostic testing, laboratory specimen collection, communications with patients, study sponsors, and investigators, and other interesting research related roles. Use approved source documents; obtain protocol-specific data to complete and maintain source documents and case report forms (including electronic data capture - EDC) in accordance with applicable regulations and sponsor requirements.
Clinical Research Patient Recruiter (31493) GI AllianceClinical Research Patient Recruiter (31493)Germantown, TNThis role involves utilizing multiple software systems and data sources to track potential participants, work closely with research coordinators to ensure proper evaluation, and guiding patients through the enrollment and exclusion process. Utilizing the above tools, and any other relevant and available sources, the Recruitment Specialist will work with the Research team and the clinical practice to develop strategies and workflows to identify and contact patients who may be candidates for clinical trials.
Clinical Research Associate I or Clinical Research Associate II St. Jude Children's Research HospitalClinical Research Associate I or Clinical Research Associate IIMemphis, TennesseeActs as site Study Coordinator by maintaining essential study documents (Investigator File) for assigned protocols, conducting informed consent process as designated by principal investigator (PI), and assisting PI with protocol submissions (internally sponsored and/or externally sponsored) for review by federal or institutional committees (e.g. (LC: SOCRA or ACRP) Certification in clinical research from the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP) must be obtained within three (3) years of assuming the position.
Clin/Tran Research Coord II Vanderbilt University Medical CenterClin/Tran Research Coord IINashville, TNEngages in open and positive communication with study participants and coworkers With direction, performs or instructs others in performing procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and in a timely manner reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine if a protocol amendment or other safety reporting to appropriate funding/regulatory agencies is required. Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants.
Research Data Specialist |Trauma | Le Bonheur | Full-Time | Days Methodist Le Bonheur HealthcareResearch Data Specialist |Trauma | Le Bonheur | Full-Time | DaysMemphis, TNWorking at MLH means carrying the mission forward of caring for our community and impacting the lives of patients in every way through compassion, a deliberate focus on service expectations and a consistent thriving for excellence. The Associate is required to have close visual acuity including color, depth perception, and field of vision to perform an activity, such as preparing and analyzing data and figures; transcribing; viewing a computer terminal; or extensive reading.
Manager, Phase II/III Research - Full Time - Wolf River West Cancer CenterManager, Phase II/III Research - Full Time - Wolf RiverGermantown, TNBachelor's degree from an accredited four-year college or university with a minimum of three (3) years of related experience; OR five (5) to seven (7) years of related experience and/or training in a healthcare or clinical research environment; OR an equivalent combination of education and experience. This role oversees Clinical Research Coordinators (CRCs), supports patients enrolled on Phase II/III clinical trials, and provides leadership for projects involving academic partners.
Intermediate Clinical Research Systems Analyst Baptist Memorial Health Care CorpIntermediate Clinical Research Systems AnalystMemphis, TNThe job responsibilities are: Work closely with Clinical Research Nurses/Coordinators, Clinical Research Data Managers, Clinical Research Management Team, and Budgets and Contracts Specialists in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, and institutional policies and procedures and departmental SOPs to provide on-going support for entering clinical research information into clinical research applications, developing and maintaining accurate databases for clinical research studies. Job Summary: This position works within the Baptist Clinical Research Institute (BCRI) and is overall, responsible for all Clinical Trial Management System (CTMS) and clinical trial applications (e-Regulatory, REDCap, EPIC/Research, EHR-to-EDC applications), and coordinates all technical aspects of the development, implementation, maintenance, and evaluation of the vendor applications supporting clinical research.
Senior Clinical Research Associate RN - Department of Infectious Diseases St. Jude Children's Research HospitalSenior Clinical Research Associate RN - Department of Infectious DiseasesMemphis, TennesseeThis is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. (As applicable) Provide patient care, education, and management (e.g., routine test conduct; assistance in clinical procedures; medication instruction, monitoring, and documentation; patient care coordination; education on protocol activities).
NewManager, Research Early Phase Program Tennessee OncologyManager, Research Early Phase ProgramNashville, TennesseeWorking collaboratively with physicians, advanced practice providers, research nurses, clinical research coordinators, clinic leadership, and SOC staff, the Manager oversees patient screening workflows, monitors operational performance, coordinates multidisciplinary communication, and drives continuous process improvement. This role is responsible for identifying and tracking potential clinical trial participants, optimizing patient enrollment, maintaining program performance metrics, and leading quality and safety initiatives that support the successful execution of the Phase I Unit and other early phase oncology studies in a community oncology setting.
["Coordinator-Budget Contract","Coordinator-Budget Contract"] Mississippi Baptist Health Systems["Coordinator-Budget Contract","Coordinator-Budget Contract"]MemphisThe role collaborates closely with Legal, Finance, Privacy & Security, research clinics, study teams, and external sponsors, exercising independent judgment on complex contract terms, budgeting decisions, and billing resolutions. This role analyzes and finalizes site budgets, prepares and submits sponsor invoices, tracks research revenue, reconciles payments, and maintains contract documentation while ensuring full compliance with sponsor, federal, Medicare Cost Analysis, and institutional guidelines.
Clin/Tran Research Coord II (Sleep Tech) Vanderbilt University Medical CenterClin/Tran Research Coord II (Sleep Tech)Nashville, TNServes as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants. Aligning with Vanderbilt Health's Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.
Clin/Tran Research Coord II (Sleep Tech) Vanderbilt HealthClin/Tran Research Coord II (Sleep Tech)Nashville, TNServes as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants. Aligning with Vanderbilt Health's Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.
Coordinator-Budget Contract Baptist Memorial Health Care CorpCoordinator-Budget ContractMemphis, TNThe Budgeting, Billing, and Contracting Coordinator is responsible for overseeing the development, negotiation, execution, and financial management of research study contracts and budgets to ensure. clinics, study teams, and external sponsors, exercising independent judgment on complex contract terms, budgeting decisions, and billing resolutions.
Care Coordinator Integrated Resources, IncCare CoordinatorChattanooga, TennesseeFull timeJob DescriptionThe care coordinator will perform the following essential activities of care coordination: Assessment – The care coordinator will assess information about a members' medical care needs, social situation and functioning to identify individual needs in order to identify members medical needs and develop a plan of care that will address those needs. Exceptional skills of independence, organization, communication, problem-solving, professional interaction, and human relation skills, as well as analytical skills and problem solving ability Ability to work within specified timeframe requirements.
RN Care Coordinator Integrated Resources, IncRN Care CoordinatorChattanooga, TennesseeContractorResponsibilities:The care coordinator will perform the following essential activities of care coordination:· Assessment -The care coordinator will assess information about a members' medical care needs, social situation and functioning to identify individual needs in order to identify members medical needs and develop a plan of care that will address those needs.· Job DescriptionTitle: Care CoordinatorDuration: 3 months (Possible extension)Location: Chattanooga, TNQualifications:Registered Nurse with active license in the state of Tennessee or hold a license in the state of their residence if the state is participating in the Nurse Licensure Compact Law.