Sonora Quest LaboratoriesTechnical Coordinator Sonora Quest LaboratoriesTechnical CoordinatorPhoenix, AZAssociate degree in a medical laboratory technology, medical laboratory science or clinical laboratory science with four (4) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area OR. Bachelor's degree in chemical or biological science (transcripts will be reviewed to determine eligibility) with two (2) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area.
Sonora Quest LaboratoriesNewLaboratory Technical Coordinator - Banner Boswell (Day Shift) Sonora Quest LaboratoriesLaboratory Technical Coordinator - Banner Boswell (Day Shift)Sun City, AZAssociate degree in a medical laboratory technology, medical laboratory science or clinical laboratory science with four (4) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area ORBachelor's degree in chemical or biological science (transcripts will be reviewed to determine eligibility) with two (2) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area. For certain specialty disciplines ONLY (Toxicology, HLA, HCTT, etc.) where no certification is available from a certifying agency, a bachelor's degree with four (4) years of experience in that discipline is required.
Sonora Quest LaboratoriesTechnical Coordinator - Blood Bank Sonora Quest LaboratoriesTechnical Coordinator - Blood BankCasa Grande, AZAssociate degree in a medical laboratory technology, medical laboratory science or clinical laboratory science with four (4) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area ORBachelor's degree in chemical or biological science (transcripts will be reviewed to determine eligibility) with two (2) years of laboratory training or experience, or both in nonwaived testing, in the designated specialty/sub-specialty area. Bachelor's Degree in medical laboratory science/medical technology, ORBachelor's degree in chemical or biological science (transcripts may be reviewed to determine eligibility) AND certification (MLS or categorical).
Mayo ClinicNewRegistered Nurse - Transplant Coordinator, Living Donor - RN Mayo ClinicRegistered Nurse - Transplant Coordinator, Living Donor - RNPhoenix, AZ$90,604.80–$136,011.20 / yearToday, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Coordinators in Bone Marrow Transplant must obtain Adult or Pediatric Oncology Certification (OCN or CPHON), or Bone Marrow Transplant Certified Nurse (BMTCN) credential within three years of hire.
Sonora Quest LaboratoriesNewPhlebotomy Coordinator Sonora Quest LaboratoriesPhlebotomy CoordinatorTucson, AZExceptional customer service skills and advanced computer skills in multiple systems to include Laboratory Information Systems and Hospital Information Systems, as well as ability to use multiple software programs. Provides technical and procedural shift supervision (determine schedules, manage day to day workflow and give input into an assessment or disciplinary action) in coordination with management.
Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate)Phoenix, AZRemoteConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol Communication with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward Verification that the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/drug accountability and inventory Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Must have a minimum of a Bachelor's degree in a health or science related field Experience as a Clinical Research Coordinator (minimum 1 year) Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely Must maintain a valid driver's license and the ability to drive to monitoring sites Proficient knowledge of Microsoft Office Strong communication and presentation skills Must be detail-oriented and efficient in time management.
Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)Phoenix, ArizonaRemoteResponsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
ECN Operating LLCClinical Research Coordinator ECN Operating LLCClinical Research CoordinatorChandler, AZThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.
GI AllianceClinical Research Coordinator II GI AllianceClinical Research Coordinator IIPeoria, AZJOB RELATIONSHIPS: • Reports to the Director of Clinical Research, Vice President of Research, Regional Market President, and the physicians at the local market • Collaborates with experienced patient navigators, IT, data management, and Urology America clinical research staff. • Mentors Clinical Research Coordinators I and II, Research Assistants, and Research Interns providing guidance during new hire training, trial initiations, and transitions.
Alcanza Clinical ResearchClinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorGilbert, ArizonaScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Phoenix Children's HospitalClinical Research Coordinator Phoenix Children's HospitalClinical Research CoordinatorPhoenix, AZEnsures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), and institutional guidelines, which includes the following duties: Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area. This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol.
Actalent IncNewClinical Research Coordinator Actalent IncClinical Research CoordinatorChandler, AZ$27–$36 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
Iterative HealthNewClinical Research Coordinator I - Nurse Iterative HealthClinical Research Coordinator I - NurseSun City, AZComplete study documentation and maintenance of study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. 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.
University of ArizonaClinical Research Coordinator II University of ArizonaClinical Research Coordinator IITucson, AZCreating source documents, study specific training in accordance with study protocols and Good Clinical Practice (GCP) guidelines. Perform data collection, entry, management, and quality control checks to ensure accuracy and completeness of study data.
University of ArizonaNewClinical Research Coordinator I University of ArizonaClinical Research Coordinator ITucson, AZAdminister clinical tests and questionnaires as part of clinical research protocols (testing visual acuity, stereoacuity, tear collection, electroretinograms, imaging of retina). Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors and internal departments.
Mayo ClinicClinical Research Coordinator Mayo ClinicClinical Research CoordinatorScottsdale, AZ$31.49–$47.25 / hourMinimum Education and/or Experience Required: (Education Requirements and Experience): HS Diploma with at least 5 years of clinical research coordination/related experience OR Associate's degree/college Diploma/Certificate Program with at least 3 years of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience. Position Overview: (Major Functions and Non-Essential Functions): Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
University of ArizonaClinical Research Coordinator I - Sarver Heart Center (COM-T) University of ArizonaClinical Research Coordinator I - Sarver Heart Center (COM-T)Tucson, AZDemonstrated ability to collaborate effectively with peers, patients, management, and internal and external stakeholders fostering professional relationships that support operational efficiency, patient-centered service, and cross-functional project success. With detailed instruction assess participants during research visit perform initial review of study lab results assess for any side effects or other problems notify principal investigator of any participant reported side effects or problems.
University of ArizonaClinical Research Coordinator I, Family and Community Medicine (Full Time) University of ArizonaClinical Research Coordinator I, Family and Community Medicine (Full Time)Tucson, AZSubmits project protocols and amendments, consent forms, and recruiting materials to the University of Arizona Institutional Review Board and department for approval with oversight from supervisor. Collects participant data, enters and analyzes data, and compiles reports, adhering to project protocols.
ECN Operating LLCNewLead Clinical Research Coordinator ECN Operating LLCLead Clinical Research CoordinatorChandler, AZThe Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and coordinating the day-to-day operations of clinical research studies, while also providing site-level leadership, mentorship, and oversight to the coordinator team. Reporting to the Site Manager, the Lead CRC ensures protocol compliance, data integrity, and inspection readiness, and serves as the primary resource and first point of escalation for the coordinator group.
Lighthouse Psychiatry Brain Health CenterClinical Research Assistant (CRA) Lighthouse Psychiatry Brain Health CenterClinical Research Assistant (CRA)Gilbert, Arizona$18–$23About Lighthouse Psychiatry:Lighthouse Psychiatry is a modern outpatient mental health practice delivering evidence-based and interventional psychiatric care, including medication management, TMS, ketamine/esketamine therapy, psychotherapy, and emerging treatment modalities. Our integrative services including psychiatric medication management, counseling, TMS, qEEG, Spravato, ketamine, ADHD testing and treatment, and clinical research of novel treatments.
MindlanceClinical and Health - Clinical Research Coord II MindlanceClinical and Health - Clinical Research Coord IITuscon, AZLogs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
Banner HealthClinical Research Assistant Cardiometabolic Program Banner HealthClinical Research Assistant Cardiometabolic ProgramPhoenix, AZAs a Clinical Research Assistant supporting our Cardiometabolic Program, you will be an integral part of the patient's Banner experience looking to provide each person with the best customer service and patient care, you will coordinate scheduling and prepare for research visits, interview and evaluate potential participants to ensure they meet eligibility requirements, instruct participants concerning protocol responsibilities and obtain consent signature, create and file adequate source documentation, accurate and timely data reporting, and perform quality checks. This position is responsible for providing primary support to both investigator-initiated and pharmaceutical research studies and projects by assisting with data collection, documentation, intake/registration, maintenance of source documents, participant recruitment and retention, data entry into research systems, data audits, maintain research supply inventory, and performs administrative tasks and clinical assessments as assigned.
A.T. Still UniversityATSU - Research Project Coordinator II A.T. Still UniversityATSU - Research Project Coordinator IImesa, AZEnsure compliance with all regulatory activities and duties, at institutional, local, and/or national levels, including creating and submitting IRB applications and maintaining IRB approvals, communicating adverse events, maintaining procedural documentation, preparing for audits and monitoring visits from regulatory bodies. Act as a liaison for research subjects, investigators, IRB, sponsors, funders, collaborators, and healthcare professionals, ensuring effective communication with all stakeholders.
Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - West Coast - RemotePhoenix, AZRemoteTypically 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.
Thermo Fisher Scientific IncClinical Research Associate II - Central/West - Oncology, Ophthalmology Thermo Fisher Scientific IncClinical Research Associate II - Central/West - Oncology, OphthalmologyAZWhat Youll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
ICON PlcClinical Research Associate ICON PlcClinical Research AssociatePhoenix, AZ$91,336–$114,170 / yearWilling and able to travel up to 60% for on-site monitoring visits across the West region; preference given to candidates residing in West region near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
University of ArizonaClinical Research Assistant (Department of Surgery) University of ArizonaClinical Research Assistant (Department of Surgery)Tucson, AZThis includes: • Completing intake for patients • Meeting IRB requirements, including calling patients and meeting with them to discuss requirements for the study • Serving as patient resource for concerns and providing information • Assisting with patient follow-up calls and appointments. Assist senior lab members in the development of written operating procedures for clinical trial and assist senior lab members with submitting required documentation to IRB.
ECN Operating LLCClinical Research Pharmacist ECN Operating LLCClinical Research PharmacistScottsdale, AZSterile Compounding (USP ): Maintain a sterile environment for preparing sterile compounds and apply rigorous aseptic techniques to prevent contamination and ensure patient safety. Monitor Visits: Meet with Clinical Research Associates (CRAs) during monitoring visits to review pharmacy binders, drug accountability records, and resolve queries.
StratAcuity Staffing Partners IncClinical Study Coordinator StratAcuity Staffing Partners IncClinical Study CoordinatorPhoenix, AZIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
Castle BiosciencesClinical Research, Regulatory Associate Castle BiosciencesClinical Research, Regulatory AssociatePhoenix, AZA typical day includes collecting and reviewing critical regulatory documents to support study start‑up, maintenance, and close‑out, ensuring documents submitted by CRAs are complete, compliant, and filed accurately in CTMS or TMF systems. The Regulatory Associate regularly reviews TMF inventories to identify missing, incomplete, or expiring documents and communicates gaps to study team members.
State of ArizonaClinical Quality Management Coordinator State of ArizonaClinical Quality Management CoordinatorPhoenix, AZRemoteProvide education and technical assistance to internal and external stakeholders, as appropriate, regarding covered services, and contractual or policy requirements, accurately and consistently to improve compliance with AHCCCS requirements and improve quality of care and service to AHCCCS members. This position will complete comprehensive assessments of available resources on service providers and individual members; review case material to ensure compliance with State and Federal regulations and policies; and provide timely resolution of multiple cases assigned.
Castle Biosciences IncClinical Research, Regulatory Associate (PHX) Castle Biosciences IncClinical Research, Regulatory Associate (PHX)Phoenix, AZServing as a regulatory resource, this role supports preparation of regulatory submissions and advises study teams on Good Clinical Practice (GCP), FDA, and applicable regulatory requirements. Castle Biosciences, Inc. is growing, and we are looking to hire a full-time Clinical Research Regulatory Associate working from our Phoenix, AZ office location with a start date of May 15, 2026.
Banner HealthSenior Clinical Research Financial Analyst Banner HealthSenior Clinical Research Financial AnalystAZ$30.56–$50.93 / hourBMDACC conducts Phases I-III clinical trials covering all Oncology disease groups with the goal to provide support to the physician investigators and to provide trial treatment options to the patients in a safe and ethical manner, while ensuring compliance to the FDA, billing entities, and institutional regulations. Acts as a liaison between finance departments, patient financial services, facility research directors and system reimbursement services for the purpose of communicating information regarding the National Coverage Decision for clinical trials and other federal research regulations.
CommonSpirit HealthClinical Research Specialist CommonSpirit HealthClinical Research SpecialistPhoenix, AZJoseph's includes the internationally renowned Barrow Neurological Institute, Norton Thoracic Institute, Cancer Center at St. Joseph's, Ivy Brain Tumor Center, and St. Every day you will manage trial activities, including participant recruitment, data collection, and documentation, serving as a key liaison for all stakeholders.
University of ArizonaResearch Compliance Administrator II, Office of Research (College of Medicine-Phoenix) University of ArizonaResearch Compliance Administrator II, Office of Research (College of Medicine-Phoenix)Phoenix, AZClinical Trial Start Up: Work independently to support the regulatory packet submission of new protocols (drug/device, industry sponsored, investigator-initiated, national cooperative group) across multiple departments for regulatory review and approval from intake of regulatory packet through hospital feasibility and IRB approvals. Regulatory Maintenance: Prepare and maintain regulatory documentation binders for internal and externally sponsored clinical studies as required by IRB, regulatory bodies and sponsors including IRB approvals, amendments, sponsor and regulatory communications.
Iterative Scopes IncNewResearch Assistant - Tucson, AZ Iterative Scopes IncResearch Assistant - Tucson, AZTucson, AZAssists Study Team in completing study documentation and maintenance of study files in accordance with sponsor requirements and site policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. 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.
University of ArizonaResearch Nurse III, Department of Internal Medicine (College of Medicine-Phoenix) University of ArizonaResearch Nurse III, Department of Internal Medicine (College of Medicine-Phoenix)Phoenix, AZTrain, oversee, and provide current patient information to clinical nurses and other health care personnel in order to assure comprehensive patient care. Adverse event and protocol deviation reporting: Report and document adverse events and protocol deviations promptly.
Mayo ClinicNewSenior Program Coordinator - Dermatology Mayo ClinicSenior Program Coordinator - DermatologyScottsdale, AZ$78,270.40–$117,312 / yearIn lieu of Bachelor's degree, Associate's degree/college Diploma/Certificate Program with 5 years of experience in clinical research/related field OR HS Diploma with at least 7 years of clinical research coordination/related experience may be considered. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations.
Banner HealthClinical Faculty: Pediatric Neurology | University of Arizona Banner HealthClinical Faculty: Pediatric Neurology | University of ArizonaTucson, AZThis position offers an exciting opportunity to provide comprehensive neurological care to pediatric patients in both ambulatory and inpatient settings, primarily at the Banner Diamond Children s Medical Center and associated outpatient clinics located within minutes of the hospital. The Department of Neurology at the University of Arizona College of Medicine Tucson, in collaboration with Banner University Medicine Tucson, seeks Board Certified/Board Eligible Pediatric Neurologists to join our growing interdisciplinary clinical faculty team.
Southern California UniversityProgram Coordinator, Doctor of Chiropractic Program, Phoenix Metro, Arizona Southern California UniversityProgram Coordinator, Doctor of Chiropractic Program, Phoenix Metro, ArizonaTempe, AZ$90,000–$113,000The PC works with the Executive Dean of the College of Chiropractic Education (ED) on the operations and the delivery of the program in Arizona, ensuring academic excellence and accreditation compliance; provides an outstanding student experience; manages faculty and staff; participates in the budget operation and program planning initiatives; promotes service, scholarship and development to faculty as needed; and fosters an environment and work culture that elevates the chiropractic program’s reputation. Onsite activities may include but are not limited to the following: meeting with students or other stakeholders, supporting admissions activities, official events, teaching and teaching observation, clinical site evaluation, patient care, accreditation activities, and others as needed to maintain quality, relevance, innovation, and marketability of the program, as well as full program compliance.
ECN Operating LLCRegulatory Coordinator ECN Operating LLCRegulatory CoordinatorChandler, AZElite Clinical Network is seeking for a Regulatory Coordinator to play a key role in ensuring clinical trial compliance by preparing, submitting, and maintaining all regulatory documents required for study initiation and conduct. Prepare, submit, and maintain all essential regulatory documents (e.g., Form 1572, CVs, medical licenses, financial disclosures, IRB submissions, etc.) for clinical trials.
Banner HealthNeuromuscular or EMG Clinical Neurophysiology Specialist | Banner/Univ. of AZ Banner HealthNeuromuscular or EMG Clinical Neurophysiology Specialist | Banner/Univ. of AZTucson, AZThe Department of Neurology at the University of Arizona College of Medicine Tucson, in collaboration with Banner University Medicine Tucson, seeks a Board Certified/Board Eligible Neuromuscular or Board Certified/Board Eligible EMG Clinical Neurophysiologist to join our dynamic and collegial clinical faculty team. Our facilities include state-of-the-art outpatient clinics, a dedicated neuromuscular genetics program with an on-site genetic counselor, neuropsychology services, and a multidisciplinary ALS clinic integrating physical, occupational, and speech therapies.
Charlie HealthNewClinical Practicum Intern (Master's Level) Charlie HealthClinical Practicum Intern (Master's Level)Phoenix, AZCharlie Health is seeking passionate and driven second-year master's students in mental health programs (such as Social Work, Clinical Mental Health Counseling, Marriage and Family Therapy, or related fields) to join our dynamic virtual care team for their clinical practicum or internship experience. As a clinical practicum student at Charlie Health, you'll gain direct experience working with high-acuity clients in a virtual Intensive Outpatient Program (IOP) setting.
Northern Arizona UniversityNewHybrid DPT Program - Assistant Clinical Professor Northern Arizona UniversityHybrid DPT Program - Assistant Clinical ProfessorFlagstaff, ArizonaA CEBE approach seamlessly aligns outcomes and assessment processes throughout a curriculum of didactic and clinical education courses to prepare graduates for the demands of physical therapy clinical practice. If you would like a free paper copy of the report, please contact the NAUPD Records Department at (928) 523-8884 or by visiting the department at 525 E. Pine Knoll Drive in Flagstaff.
Mayo ClinicFaculty Position in Health Care Delivery Research Mayo ClinicFaculty Position in Health Care Delivery ResearchPhoenix, AZWe also collaborate to develop, assess and implement new methods of care delivery - such as telehealth specialty care for children with sickle cell disease and virtual nurse care team members - to reduce healthcare disparities and lead to better patient outcomes. As the only research center fully embedded in the medical practice, the Mayo Clinic Kern Center for the Science of Health Care Delivery is uniquely positioned to advance Mayo Clinic's history of taking a scientific approach to healthcare delivery.
City of HopeResearch Associate III City of HopeResearch Associate IIIPhoenix, AZCompletion of projects can involve manual or robotic nucleic acid extractions, sequencing library preparation, loading and maintaining sequencing instruments, detailed record-keeping using a laboratory information management system, evaluation of pre- and post-sequencing quality control metrics. A hallmark of TGen is our belief that by utilizing the latest technologies and collaborating with the strongest of partners, we can develop better tools to increase our understanding of complex diseases and to better predict which treatments might be most effective, i.e., one-of-a-kind clinical trials (the right drug, at the right dose, at the right time).
Colgate-Palmolive CompanyNewResearch Associate (Scottsdale, AZ, US) Colgate-Palmolive CompanyResearch Associate (Scottsdale, AZ, US)Scottsdale, AZ$70,000–$96,000 / yearOur journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. Encompassing the innovative skincare brands of PCA SKIN, EltaMD, and Filorga, CP Skin Health Group is a fast-paced, agile organization dedicated to providing skin care solutions that are backed by science.
Colgate-PalmoliveNewResearch Associate Colgate-PalmoliveResearch AssociateScottsdale, AZ$70,000–$96,000 / yearFor additional Colgate terms and conditions, please click here (https://www.colgatepalmolive.com/content/dam/cp-sites/corporate/corporate/en_us/corp/locale-assets/pdf/colgate-terms-and-conditions-2023.pdf) . Encompassing the innovative skincare brands of PCA SKIN, EltaMD, and Filorga, CP Skin Health Group is a fast-paced, agile organization dedicated to providing skin care solutions that are backed by science.
Bertelsmann SE & Co KgaAProgram Director and Core Faculty Clinical Psychology Phoenix Campus Bertelsmann SE & Co KgaAProgram Director and Core Faculty Clinical Psychology Phoenix CampusPhoenix, AZThe Program Director manages academic and program functions, oversees program assessment, continuous improvement, interventions, and accreditation, leads and/or facilitates student sessions such as workshops and orientations, provides educational guidance for new and continuing students, assists in the development and implementation of student learning outcomes, leads and/or participates in curriculum development, faculty development, and applicable university and/or program activities. Prior to program launch, the position is 1.0 FTE program director with a focus on program development, including building program materials, preparing a self-study, developing practicum sites, and recruiting core and adjunct faculty.
The Translational Genomics Research InstituteResearch Associate III The Translational Genomics Research InstituteResearch Associate IIIPhoenix, AZCompletion of projects can involve manual or robotic nucleic acid extractions, sequencing library preparation, loading and maintaining sequencing instruments, detailed record-keeping using a laboratory information management system, evaluation of pre- and post-sequencing quality control metrics. A hallmark of TGen is our belief that by utilizing the latest technologies and collaborating with the strongest of partners, we can develop better tools to increase our understanding of complex diseases and to better predict which treatments might be most effective, i.e., one-of-a-kind clinical trials (the right drug, at the right dose, at the right time).