NewBilingual Clinical Research Coordinator II (English and Spanish) Johnson County ClintrialsBilingual Clinical Research Coordinator II (English and Spanish)Houston, TXBy applying advanced knowledge of study protocols, strong organizational skills, and sound judgment, the Clinical Research Coordinator II contributes to the timely, efficient, and high-quality conduct of clinical studies that advance research objectives and improve patient outcomes. The purpose of the Clinical Research Coordinator II role is to ensure the successful execution of multiple concurrent clinical trials through effective study coordination, subject management, and cross-functional communication.
NewClinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorSugar Land, TXScheduling 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;].
NewRN Clinical Supervisor - Hybrid Schedule Aveanna HealthcareRN Clinical Supervisor - Hybrid ScheduleHouston, TX$66,000 / yearSee Aveanna Healthcare Terms & Conditions at https://www.aveanna.com/privacypolicy.html and Privacy Policy at https://www.aveanna.com/privacypolicy.html and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions. As an employer accepting Medicare and Medicaid funds, employees must comply with all health-related requirements in all relevant jurisdictions, including required vaccinations and testing, subject to exemptions for medical or religious reasons as appropriate.
NewClinical Research Coordinator aQua DialysisClinical Research CoordinatorHouston, TXConcrete background in medicine· Thorough knowledge of medical research· Excellent verbal and written communication skills· Proficiency with computers, especially Microsoft office· Knowledgeable about ICH Guidelines, GCPs, as well as FDA regulations· Able to handle multiple protocols in various therapeutic areas· Must be detailed oriented· Must be willing to travel to various locations in Greater Houston Education Experience· Bachelors required, Master degree preferred.· Maintains strict patient confidentiality according to HIPAA regulations and applicable law.· Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs guidelines· Contribute to growth of company with future supervisory role REQUIREMENTS:· Great at customer service· Self-motivated/starter· Outgoing, excellent recruiting skills· Phlebotomy experiences a MUST.·
NewClinical Research Coordinator -Traveling PRN Alcanza Clinical ResearchClinical Research Coordinator -Traveling PRNSugar Land, TXResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 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; Scheduling 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. Skills, Knowledge and Expertise Minimum Qualifications : A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.
NewAdjunct Professor - Clinical Mental Health Counseling University of St. ThomasAdjunct Professor - Clinical Mental Health CounselingHouston, TXThomas (UST), a private Catholic University committed to the liberal arts and the religious and intellectual tradition of Catholic higher education, located in Houston, Texas, near the vibrant central business district, Texas Medical Center, and museum district, is seeking applicants for an adjunct faculty position to teach various graduate clinical mental health counseling courses in the CACREP-accredited department. EXPERIENCE:Teaching experience at the graduate level in counseling or related fields; ability to teach in aface-to-face format and demonstrated excellence in teaching.
NewClinical Psychologist (Ph.D., Psy.D, Ed.D., or LSSP) Ethos WellnessClinical Psychologist (Ph.D., Psy.D, Ed.D., or LSSP)Houston, TXThe primary role of this position is to conduct comprehensive neuropsychological and psychoeducational evaluations for children and adolescents for concerns related to academic performance, ADHD, specific learning disorders, giftedness, Autism Spectrum Disorder, mental health conditions, and more. The expectation for the testing process includes consultation with parents, administration of testing, generating thorough reports of findings, and communicating results efficiently and effectively with parents and schools as needed.
Research Coordinator II - Cancer - Clinical Trials Clinical Studies Houston Methodist HospitalResearch Coordinator II - Cancer - Clinical Trials Clinical StudiesHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
Part time Clinical Nurse - Clinical & Translational Research Center University of Texas MD Anderson Cancer CenterPart time Clinical Nurse - Clinical & Translational Research CenterHouston, TXWith a 41-bed treatment area and a full-function laboratory, the 12,660-square-foot CTRC provides a dedicated environment for first-in-human and Phase I and II clinical research where innovation meets patient care. The Clinical & Translational Research Center (CTRC) is the hub for groundbreaking early-phase clinical trials, supporting more than 700 cutting-edge studies across 22 departments.
Clinical Nurse - Clinical & Translational Research Center University of Texas MD Anderson Cancer CenterClinical Nurse - Clinical & Translational Research CenterHouston, TXSpecific competencies include: IV insertion and venous access device management; Accurate administration and monitoring of infusions via a variety of routes (oral, subcutaneous, intramuscular, intravenous); Performing an independent double-check for chemotherapy administration; Safe handling and disposal of chemotherapy to minimize patient and staff exposure to hazardous drugs; Management of treatment-related side effects and adverse reactions; Minimizing the risk for infection among patients who are actually or potentially immunocompromised; Knowledge needed to facilitate early detection of specific side effects that lead to effective self-management of the side effect when it does occur. Advanced Cardiac Life Support (ACLS) certification and Pediatric Advanced Life Support (PALS) certification if working in the following department: Nrsg Post Anesthesia Care Unit (600160).
Assistant Professor, Clinical Faculty Appointment (CFA) - Clinical Cancer Prevention MD AndersonAssistant Professor, Clinical Faculty Appointment (CFA) - Clinical Cancer PreventionHouston, TXThis position will provide clinical services primarily at MD Anderson's Cancer Prevention Center locations, including the Texas Medical Center - Fannin, Northwest Houston, and Missouri City, with designated protected time allocated for research and educational activities. The Clinical Cancer Prevention Department is a multidisciplinary department whose members conducts basic, translational, and cancer prevention clinical research, and provides clinical cancer prevention services and education.
Clinical Research Associate (Cra) - Cardiovascular/Vaccine/Infectious Disease- Remote Merck & Co., Inc.Clinical Research Associate (Cra) - Cardiovascular/Vaccine/Infectious Disease- RemoteHouston, TXRemote$96,200–$151,400 / yearRequired Skills: Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies, Data Analysis, Data Reporting, Early Clinical Development, Policy Development, Preventive Action, Protocol Adherence, Regulatory Compliance, Site Management. Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote Merck & Co IncClinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- RemoteHouston, TXRemote$96,200–$151,400 / yearRequired Skills: Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies, Data Analysis, Data Reporting, Early Clinical Development, Policy Development, Preventive Action, Protocol Adherence, Regulatory Compliance, Site Management. Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Clinical Research Systems Manager MD AndersonClinical Research Systems ManagerHouston, TXRemoteThe Clinical Research Systems Manager ensures ensures the integrity, availability, and appropriate use of CTMS data across the clinical trial lifecycle while leading complex technical projects that advance research efficiency, compliance, and reporting capabilities. The position offers opportunities to lead complex technical initiatives, collaborate with research and technology experts, and shape infrastructure that supports institutional growth, professional development, and work-life balance.
Clinical Protocol Administration Manager - Pediatrics Research University of Texas MD Anderson Cancer CenterClinical Protocol Administration Manager - Pediatrics ResearchHouston, TXYou will also champion quality, compliance, and continuous improvement by overseeing quality assurance initiatives, preparing teams for sponsor audits, monitoring protocol compliance, implementing corrective and preventive action plans (CAPAs), evaluating quality metrics, and leading operational improvements that enhance research performance and regulatory readiness. MD Anderson offers a comprehensive total rewards package, including paid medical benefits, generous paid time off, retirement plans, tuition assistance, professional development opportunities, and additional benefits, along with the opportunity to build a rewarding leadership career at one of the world's leading cancer centers while helping shape the future of pediatric oncology research and bringing innovative therapies to children and young adults facing cancer.
Manager of Clinical Documentation (CCDS Required) - Clinical Data Management University of Texas Medical Branch at GalvestonManager of Clinical Documentation (CCDS Required) - Clinical Data ManagementGalveston, TXThe CDI Manager will work in collaboration with CDI specialists, clinicians, coders, and all members of the healthcare team to ensure accurate and timely clinical documentation within the medical record. Provide direction for the provision of education to the medical staff and the healthcare team regarding clinical documentation opportunities, coding and reimbursement issues, as well as performance improvement methodologies.
NewClinical - Clinical Pharmacist 1 - 210392 Pacer GroupClinical - Clinical Pharmacist 1 - 210392Houston, TXRemote$60–$65In this role, you will review prior authorization and appeal requests to help ensure members receive the right medications based on clinical guidelines and health plan policies. You will work with healthcare providers, pharmacy technicians, and internal teams to make accurate and timely coverage decisions.
Sr. Clinical Research Nurse - Transplant Center Houston Methodist HospitalSr. Clinical Research Nurse - Transplant CenterHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Assists Principal Investigator to ensure that all persons 'engaged' in research studies have met training requirements in accordance with Federal regulations and entity policies and procedures including preparing Institutional Review Board (IRB) and regulatory documents following ICH/GCP guidelines, and the development of materials and tools necessary to appropriately facilitate the conduct of research.
Clinical Trial Program Manager - Neurology (Neurodegenerative division) University of Texas Health Science Center at HoustonClinical Trial Program Manager - Neurology (Neurodegenerative division)Houston, TXRegistered Nurse (RN) State Licensure or Nurse Licensure Compact (NLC) by Texas Board of Nursing (BON) depending on clinical trial, may be required Human Subjects Research (HSR) by Collaborative Institutional Training Initiative (CITI Program) depending on clinical trial, may be requiredMinimum Education:Bachelor''s Degree required In the event that an RN degree is required, the bachelor''s degree may be waivedMinimum Experience:5 years of relevant experience required Pharmaceutical or clinical research strongly preferredPhysical Requirements:Exerts up to 100 pounds of force occasionally and/or up to 50 pounds frequently and/or up to 20 pounds constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Clinical Research Coordinator II - Nurse Iterative Scopes Inc.Clinical Research Coordinator II - NurseWebster, TXBy 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. 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.