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 Coordinator Respiratory Therapy TriStar Summit Medical CenterClinical Coordinator Respiratory TherapyHermitage, TNAdditional benefits for fertility and family building, adoption assistance, life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection and consumer discounts. What you will do in this role: Participate in all phases of the arterial blood gas laboratory, including responsibility of all necessary studies, QA/QI, PI testing, maintenance, reporting and competencies.
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 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.
Research Nurse Coordinator-Office of Clinical Research University of Tennessee SystemResearch Nurse Coordinator-Office of Clinical ResearchMemphis, TNJOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Nurse Coordinator- Oncology oversees the daily operations of the oncology clinical trials, including study coordination, regulatory compliance, IRB activities, data management, and research oversight under the direction of the Principal Investigator. Utilizes oncology nursing expertise to assess, document, and report patient responses to investigational therapies, including adverse events, toxicities, and treatment outcomes while monitoring protocol compliance, treatment tolerance, symptom management, ant treatment interruptions.
Clinical Research Coordinator II Care AccessClinical 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.
Clinical Research Coordinator II - Hermitage, TN Iterative Scopes IncClinical Research Coordinator II - Hermitage, TNTNLead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
Clinical Research Coordinator I Ora IncClinical 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 II - Hermitage, TN Iterative HealthClinical Research Coordinator II - Hermitage, TNHermitage, TNBy combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals.
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 I - Nurse - Cordova, TN Iterative Scopes IncClinical Research Coordinator I - Nurse - Cordova, TNTNBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
Clinical Research Coordinator II Tennesssee 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 I - Nurse Iterative HealthClinical Research Coordinator I - NurseCordova, TNWe built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
NewClinical Research Coordinator K2 Staffing LLCClinical Research CoordinatorBerry Hill, TNPrimary Responsibilities: Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator Articulate all pertinent issues to the Pl or document by email/letter or during meetings Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical Research Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging Maintain timely K2 Medical Research source documentation as well as sponsor required information. Complete all monitor and sponsor queries in a timely manner Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study Knowledge, Skills, and Abilities: Outstanding verbal and written communication skills Excellent interpersonal and customer services skills Strong time management and organizational skills In depth knowledge of industry regulations Proven ability to and foster mentoring relationships Ability to create momentum and foster organizational change Qualifications: HS Diploma or GED Transcript required.
Clinical Research Coordinator, Ripley TN Medovation Clinical Research LLCClinical Research Coordinator, Ripley TNRipley, TNWe are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies.
Clinical Research Coordinator - Float US Oncology IncClinical Research Coordinator - FloatMemphis, TNCookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
Clinical Research Coordinator HCA HealthcareClinical Research CoordinatorNashville, TNEnsures 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. The Clinical Research Coordinator position is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors.
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.
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.
Clinical Research Coordinator East Tennessee State UniversityClinical Research CoordinatorJohnson City, TNThe Clinical Research Coordinator will interface basic researchers and clinicians by facilitating specimen accrual to translational studies, particularly a new initiative with UTHSC focusing on genomic data merged with clinical data. Aligned with the institution''s mission, we value efforts to engage in teaching, scholarship, creative activities, and service that involve community partners and address significant societal needs in our region and beyond.
Clinical Research Coordinator (31205) GI AllianceClinical Research Coordinator (31205)Germantown, TNActs as an experienced resource for Clinical Research Coordinators I and Research Assistants during new hire training, newly initiated trials, and trial transitions. JOB RELATIONSHIPS: Reports to the Clinical Research Director, Vice President of Research, Market President, and the physicians at the local Market Clinic.
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 Associate II or Clinical Research Associate II RN - Bioethics Program St. Jude Children's Research Hospital IncClinical Research Associate II or Clinical Research Associate II RN - Bioethics ProgramMemphis, TN$70,720–$126,880 / yearThe program is led by two core faculty - Dr. Liza-Marie Johnson, whose scholarship focuses on clinical and research ethics with particular emphasis on informed consent, patient-provider communication, and the ethics of novel interventions - and Dr. Meaghann Weaver, whose work spans bioethics, palliative care, quality of life, and end-of-life decision-making for seriously ill children. Research themes across the program include ethical issues in pediatric genomic sequencing, communication and decision-making with seriously ill children and their families, the allocation of emerging therapies, and the experience of suffering and end-of-life care in pediatric populations.
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).
Clinical Research Associate II St. Jude Children's Research HospitalClinical Research Associate IIMemphis, 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. The Clinical Research Associate II in this team is responsible for supporting clinical research activities through data abstraction, data curation, data management, quality assurance, participant reporting, and process improvement.
Clinical Research Assistant Care AccessClinical Research AssistantMemphis, TNRemote$19–$33 / hourWith 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 Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
Clinical Research Assistant Care Access Research LLCClinical Research AssistantMemphis, TN$19–$33 / hourWith 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 Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
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.
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.
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.
NewResearch 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 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 Study Coordinator PSI CRO AGClinical Study CoordinatorCleveland, TNTasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects.
Clinical Research Assistant University Physicians Association IncClinical Research AssistantKnoxville, TNKey Responsibilities • Assist with the day-to-day operations of clinical research studies and trials • Support participant recruitment, screening, enrollment, and follow-up activities • Collect, record, and maintain accurate study data in case report forms (CRFs), electronic data capture systems, and source documents • Prepare and maintain regulatory binders and study documentation in accordance with IRB, GCP, and sponsor requirements • Coordinate study visits, schedules, and communications with participants and study staff • Assist with informed consent processes under the supervision of authorized personnel • Perform basic clinical tasks as permitted (e.g., vital signs, specimen handling, questionnaire administration) • Able to do lab draws on patients • Support monitoring visits, audits, and inspections • Ensure confidentiality and proper handling of protected health information (PHI) • Communicate effectively with investigators, coordinators, sponsors, and regulatory bodies • Assist with inventory management of study supplies and investigational products (as applicable). Skills and Competencies: • Strong time management and multitasking abilities • Professional and ethical conduct • Ability to work independently and as part of a multidisciplinary team • Problem-solving and critical-thinking skills • Comfort interacting with patients and research participants.
Clinical Research Pharmacist Tennesssee OncologyClinical Research PharmacistNashville, 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. Provide enhanced oversight for all double-blind clinical trials, including serving as primary un-blinded pharmacist, pharmacy binder maintenance, drug preparation, receipt, destruction, and data entry (when applicable).
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.
Mgr-Clinical Research Pharmacy Services St. Jude Children's Research HospitalMgr-Clinical Research Pharmacy ServicesMemphis, TennesseeD. accredited by the American Council of Pharmacy Education with PGY2 residency or 8+ years of pharmacy practice experience at St. Jude or a comparable institution; completion of a clinical pharmacy residency or fellowship in Pediatrics, Oncology, or Infectious Diseases Pharmacy can be considered in lieu of experience. This role provides leadership to a team of Clinical Pharmacy Specialists and Pharmacy Technicians dedicated to IDS operations, supporting a robust portfolio of more than 100 active clinical trials.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateTNRemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedClarksville, TNEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
NewSenior Clinical Research Associate IRESenior Clinical Research AssociateNashville, TennesseeRemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Med Surg Clinical Nurse Coordinator HCA HealthcareMed 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.
Clinical Research Associate Ascension Health AllianceClinical Research AssociateNashville, TNOur legitimate email communications will always come from an @ascension.org email address; do not trust other domains, and an official offer will only be extended to candidates who have completed a job application through our authorized applicant tracking system. Recognized as one of the Best 150+ Places to Work in Healthcare and a Military-Friendly Gold Employer, you'll find an inclusive and supportive environment where your contributions truly matter.
Clinical Research Associate II Allen SpoldenClinical Research Associate IINashville, TennesseeConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
NewClinical Research Associate I - Little Rock ArkansasMemphis Tennessee Shreveport Louisiana AbbVie IncClinical Research Associate I - Little Rock ArkansasMemphis Tennessee Shreveport LouisianaMemphis, TNRemoteApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
CLINICAL APP COORDINATOR 2 - 05192026-77598 State of TennesseeCLINICAL APP COORDINATOR 2 - 05192026-77598Nashville, TNAn incumbent in this class must have advanced knowledge of information science and technology and health care practices and processes; must be skilled in the development of operational processes for selected solutions and in creating reports; must show demonstrated proficiency with information systems technology; must be flexible, highly collaborative, and consistently work to fill gaps and avoid overlaps of system activities; must be able to continuously listen, react, and suggest ways to complement or assist the work of others; and must have a thorough understanding of the application for which he/she is responsible and has/will gain knowledge across all relevant applications. Knowledge: Advanced knowledge of administration and management relative to health care or population health business principles that may include administrative and office management procedures/systems related to health care practice management, strategic planning, leadership techniques and coordination of people and resources.
Clinical Spine Coordinator (RN), FT, Days, VUH Vanderbilt University Medical CenterClinical Spine Coordinator (RN), FT, Days, VUHNashville, TNAssists with discharge/transition planning in collaboration with the multi-disciplinary team, actively engaging outpatient care providers by sharing hospital course, concerns, pending test results, learning needs, partnership opportunities etc. Discover Vanderbilt University Medical Center: Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world.
Clinical Coordinator Respiratory Therapy HCA HealthcareClinical Coordinator Respiratory TherapyHermitage, TNAdditional benefits for fertility and family building, adoption assistance, life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection and consumer discounts. What you will do in this role: Participate in all phases of the arterial blood gas laboratory, including responsibility of all necessary studies, QA/QI, PI testing, maintenance, reporting and competencies.
NewClinical Research Assistant US Oncology IncClinical Research AssistantKnoxville, TNCookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
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