RN Adolescent Clinical Research - PRN Professional Case ManagementRN Adolescent Clinical Research - PRNMesquite, TX$55Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred) . You'll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation.
Registered Dietitian Clinical Research - PRN Professional Case ManagementRegistered Dietitian Clinical Research - PRNEl Paso, TX$42Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
NewBilingual Registered Dietitian Clinical Research - PRN Professional Case ManagementBilingual Registered Dietitian Clinical Research - PRNEl Paso, TX$42Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
NewNURSE RESEARCH COORDINATOR Methodist Health SystemNURSE RESEARCH COORDINATORDallas, TXNamed one of the fastest-growing health systems in America by Modern Healthcare , Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others. In addition to customary research coordination activities, the Nurse Research Coordinator, under the direction of the principal investigator, will perform study-related assessments and procedures, such as: physical examinations, transient elastography (TE), electrocardiogram (ECG) infusion therapy, phlebotomy, and administer medications as outlined in the research protocol.
Per Diem Physician Assistant or Nurse Practitioner (Casual Employee) One MedicalPer Diem Physician Assistant or Nurse Practitioner (Casual Employee)AUSTIN, TXOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.
NewPer Diem Family Medicine Physician Assistant or Nurse Practitioner (Casual Employee) One MedicalPer Diem Family Medicine Physician Assistant or Nurse Practitioner (Casual Employee)AUSTIN, TXOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.
NewPhysician Assistant, First Assist - General Surgery CHRISTUS HealthPhysician Assistant, First Assist - General SurgeryAlice, TXCHRISTUS SPOHN is seeking a Physician Assistant, First Assistant responsible for providing medical or surgical services to patients; collecting and documenting date, conducting diagnostic and therapeutic procedures; ordering and scheduling necessary studies and professional consultations; and providing direct patient care services to include prescribing medications and other therapies as needed to join its team at CHRISTUS Spohn Hospital in Alice, TX. The APC acts independently and/or in collaboration with the health team in the observation, assessment, diagnosis, intervention, evaluation, rehabilitation, care, counsel and health teachings of persons who are ill, injured or informed of experiencing changes in normal health processes, and in the promotion and maintenance of health or prevention of illness.
NewNurse Practitioner, NP or Physician Assistant, PA - General Surgery Shoreline CHRISTUS HealthNurse Practitioner, NP or Physician Assistant, PA - General Surgery ShorelineCorpus Christi, TXThis position is responsible for providing medical or surgical services to patients; collecting and documenting date, conducting diagnostic and therapeutic procedures; ordering and scheduling necessary studies and professional consultations; and providing direct patient care services to include prescribing medications and other therapies as needed. The APC acts independently and/or in collaboration with the health team in the observation, assessment, diagnosis, intervention, evaluation, rehabilitation, care, counsel and health teachings of persons who are ill, injured or informed of experiencing changes in normal health processes, and in the promotion and maintenance of health or prevention of illness.
NewNurse Practitioner, NP or Physician Assistant, PA - Gastroenterology CHRISTUS HealthNurse Practitioner, NP or Physician Assistant, PA - GastroenterologyCorpus Christi, TXThe Nurse Practitioner or Physician Assistant is responsible for providing medical or surgical services to patients; collecting and documenting date, conducting diagnostic and therapeutic procedures; ordering and scheduling necessary studies and professional consultations; and providing direct patient care services to include prescribing medications and other therapies as needed. The APC acts independently and/or in collaboration with the health team in the observation, assessment, diagnosis, intervention, evaluation, rehabilitation, care, counsel and health teachings of persons who are ill, injured or informed of experiencing changes in normal health processes, and in the promotion and maintenance of health or prevention of illness.
Principal Investigator (Medical Director) AtriumPrincipal Investigator (Medical Director)Austin, TX$100–$150 / hourThe organization partners with healthcare providers, Research teams, and sponsors to support high-quality clinical studies across multiple therapeutic areas while maintaining a strong commitment to patient safety, operational excellence, and scientific integrity. Responsibilities of the Principal Investigator (Medical Director): Serve as Principal Investigator (Medical Director) or Sub-Investigator for site-based and decentralized/hybrid clinical trials, ensuring patient safety, regulatory compliance, and data integrity.
NewDepartment of Cardiovascular Medicine Faculty Opportunities UTMB HealthDepartment of Cardiovascular Medicine Faculty OpportunitiesGalveston, TXHeart Failure-Transplant Cardiologist - The Department of Cardiovascular Medicine at UTMB Health, seeks an advanced Heart Failure and VAD / Transplant cardiologist to join its robust, academic cardiology practice at the level of Assistant or higher (all Academic ranks welcome). Advanced Cardiac-Imaging Cardiologist - The Department of Cardiovascular Medicine at UTMB Health, seeks an Advanced Cardiac Imaging cardiologist to join its robust, academic cardiology practice at the level of Assistant Professor or higher (all Academic ranks welcome).
Clinical Research Assistant Adams ClinicalClinical Research AssistantDallas, TX$19.23–$23.08 / hourWorking under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
NewResearch Assistant I - Orthopedic Research University of Texas Health Science Center at HoustonResearch Assistant I - Orthopedic ResearchHouston, TXOur 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! Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure.
Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research IncClinical Research Assistant Opportunities - Multiple Locations NationwideBrownsville, TXThis general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.
Clinical Research Assistant, PRN (Preferably Bilingual, Phlebotomist, LVN or Registered Nurse) Care AccessClinical Research Assistant, PRN (Preferably Bilingual, Phlebotomist, LVN or Registered Nurse)Houston, TexasWith 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. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Clinical Research Assistant Care AccessClinical Research AssistantHouston, TexasWith 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.
Research Assistant I - Psychiatry and Behavioral Sciences'''' Texas Youth Depression and Suicide Research Network (Tx-YDSRN) University of Texas Health Science Center at HoustonResearch Assistant I - Psychiatry and Behavioral Sciences'''' Texas Youth Depression and Suicide Research Network (Tx-YDSRN)Houston, TXUTHealth Houston''s Psychiatry and Behavioral Sciences'' Texas Youth Depression and Suicide Research Network (Tx-YDSRN) is looking for a strong candidate with excellent communication and interpersonal skills to recruit, see subjects, and manage regulatory and scheduling aspects of its clinical research study. 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 I Dallas Research InstituteClinical Research Coordinator IDallas, TexasComplete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs. Summary: The Clinical Research Coordinator I will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are followed.
Clinical Research Assistant Bilingual in Spanish Care Access Research LLCClinical Research Assistant Bilingual in SpanishHouston, TX$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, PRN Bilingual, Registered Nurse Care Access Research LLCClinical Research Assistant, PRN Bilingual, Registered NurseHouston, TX$19–$44 / hourAs a Clinical Research Assistant, PRN (Registered Nurse), you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life. In this event-based role, you'll: • Support participant care and event operations, including phlebotomy, specimen handling, and documentation (paper or electronic).
Clinical Research Coordinator, Ob/Gyn Research Support Unit University of Texas Medical Branch at GalvestonClinical Research Coordinator, Ob/Gyn Research Support UnitGalveston, TXAssists with grant/protocol preparation and submission to IRB, OCR or OSP under direction of research coordinator under the direction of the PI and with answering IRB stipulations to obtain final approval, documents IRB approval and contract approval. Job Duties: The duties of this role will include but are not limited to the following: Obtain human subject data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
Assistant Clinical Research Coordinator (Pasadena, CA) Profound ResearchAssistant Clinical Research Coordinator (Pasadena, CA)Pasadena, TexasAs an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting.
Clinical Research Coordinator Pinnacle Clinical ResearchClinical Research CoordinatorSan Antonio, TexasAbout Pinnacle Clinical Research: Pinnacle Clinical Research Network provides world-class clinical trial solutions to its member sites, sponsors, CROs, researchers and patients to accelerate the results of their trials. Complete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs.
Contractor- Assistant Clinical Research Coordinator (Pasadena, CA) Profound ResearchContractor- Assistant Clinical Research Coordinator (Pasadena, CA)Pasadena, TexasAs an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.
Clinical Research Coach (Onsite) Research Administration (Galveston) Certification (CCRC) University of Texas Medical Branch at GalvestonClinical Research Coach (Onsite) Research Administration (Galveston) Certification (CCRC)Galveston, TXJob Description: The primary focus of the Clinical Research Coach is to provide mentorship, instruction, and guidance to clinical research investigators, nurses, coordinators, and other study staff to promote high-quality research and implement best practices. Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) or similar certification through a recognized professional clinical research organization, or ability to obtain professional certification within one year of employment.
Sr. Coord Clinical Research, OB/GYN Research Support Unit (Galveston) University of Texas Medical Branch at GalvestonSr. Coord Clinical Research, OB/GYN Research Support Unit (Galveston)Galveston, TXMaintains accurate source documentation and appropriate forms as per protocol including participant records, drug documentation, reconciling study drug accountability; monitors documentation for quality and accuracy. Identifies and recruits clinical research subjects; monitors enrollment goals and modifies recruitment strategies, as necessary; mentors all clinical research personnel regarding enrollment/recruitment.
Research Assistant I/II - Center for Neurobehavioral Research on Addiction (CNRA) University of Texas Health Science Center at HoustonResearch Assistant I/II - Center for Neurobehavioral Research on Addiction (CNRA)Houston, TXOur 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! Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure.
Sr. Clinical Research Coordinator, Research Administration University of Texas Medical Branch at GalvestonSr. Clinical Research Coordinator, Research AdministrationGalveston, TXMaintains accurate source documentation and appropriate forms as per protocol including participant records, drug documentation, reconciling study drug accountability; monitors documentation for quality and accuracy. Identifies and recruits clinical research subjects; monitors enrollment goals and modifies recruitment strategies, as necessary; mentors all clinical research personnel regarding enrollment/recruitment.
Research Assistant II/III - OBGYN, Gynecologic Oncology University of Texas Health Science Center at HoustonResearch Assistant II/III - OBGYN, Gynecologic OncologyHouston, TXOur 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! Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure.
NewSenior Research Assistant - BRCA & Genome Instability Center University of Texas MD Anderson Cancer CenterSenior Research Assistant - BRCA & Genome Instability CenterHouston, TXThis Senior Research Assistant performs and supports technical clinical research work as a key member of the Center for BRCA and Genome Instability, a new and comprehensive institutional hub that provides cutting-edge research testing and therapeutic options, as well as high-quality care to ultimately shift treatment paradigms and improve outcomes of patients with targetable molecular BRCA and related DNA Damage Response (DDR) genetic alterations and genome instability. This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening.
Senior Research Assistant - Hematopoietic Cell Transplantation and Immuno-Oncology Baylor College of MedicineSenior Research Assistant - Hematopoietic Cell Transplantation and Immuno-OncologyHouston, TX$57,320–$67,435 / yearThe Luznik Lab at Baylor College of Medicine is seeking a highly motivated Senior Research Assistant to support translational research focused on allogeneic hematopoietic cell transplantation, immune escape, and leukemia relapse. Our group integrates murine models and patient-derived clinical samples to investigate mechanisms of post-transplant relapse and to develop novel immune-based therapies.
Site Research Assistant - McAllen, TX IQVIA Holdings IncSite Research Assistant - McAllen, TXMcAllen, TX$25–$39 / hourExperience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Clinical Research Specialist (Patient Engagement Research Lab – Department of Surgery) HMRIClinical Research Specialist (Patient Engagement Research Lab – Department of Surgery)TexasThe Clinical Research Specialist further provides general qualitative data analysis support, including assisting with coding, organizing, and synthesizing qualitative data from interviews, focus groups, and other patient centered research activities FLSA STATUS . Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities.
NewClinical Research Assistant DiaSorin SpAClinical Research AssistantAustin, TXin chemistry, biology, molecular biology or a related subject, with additional post-graduate diploma or 1 year work experience preferred but not required; OR college degree (technical subject), plus additional post-graduate diploma, plus at least 2 years work experience; OR college degree (technical subject) plus at least 3 years work experience. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios.
Clinical Research Assistant TDI University HealthClinical Research Assistant TDISan Antonio, TXAssists physicians and other health care providers in the performance of medical and laboratory tasks not requiring the services of a licensed provider. EDUCATION/EXPERIENCE High school diploma or equivalent experience required.
Research Assistant I - Cardiothoracic Vascular Surgery University of Texas Health Science Center at HoustonResearch Assistant I - Cardiothoracic Vascular SurgeryHouston, TXIn this role, you will work closely with the principal investigator to ensure the smooth execution of FDA‑regulated clinical studies, including maintaining regulatory compliance with the FDA and Institutional Review Board, coordinating consent and data collection, facilitating communication and documentation among the sponsored projects office, clinical care teams, and study sponsors, preparing progress reports, and organizing study materials and databases for monitor visits. 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!
Research Assistant I/II - Psychiatry and Behavioral Sciences'''' REaKT University of Texas Health Science Center at HoustonResearch Assistant I/II - Psychiatry and Behavioral Sciences'''' REaKTHouston, TXThe Research Assistant will perform comprehensive pre-screening assessments and detailed medical record reviews to determine participant eligibility; collect clinical, cognitive, behavioral, and biological data in accordance with study protocols; ensure participant safety by monitoring and promptly escalating concerns; collaborate closely with psychiatrists, nursing staff, ECT teams, sponsors, and research personnel to uphold protocol compliance; and provide ongoing support for data entry, quality control, and study closeout activities. This role involves direct interaction with participants experiencing major depressive disorder, treatment-resistant depression, and acute suicidal ideation who are enrolled in clinical trials evaluating electroconvulsive therapy (ECT), ketamine, and other interventional psychiatry treatments.
Clinical Research Associate (CRA) - Dallas Medpace, Inc.Clinical Research Associate (CRA) - DallasIrving (Dallas), TexasResponsibilities: 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. Qualifications: Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; 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; and.
Research Assistant ObjectiveHealth IncResearch AssistantWichita Falls, TXPossess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, lab cleanliness, and strict protocol adherence. Not easily distracted: You have the ability to stay focused while running different protocols, tracking patient reports, and maintaining eSource material for assigned studies.
Clinical Research Coordinator / Ophthalmic exp. required - Dallas Texas Retina AssociatesClinical Research Coordinator / Ophthalmic exp. required - DallasDallas, TXTexas Retina Associates is Texas’ largest, most experienced ophthalmology practice focused specifically on the diagnosis, medical and surgical management of diseases of the retina and vitreous. Present patient history summary and alert Ophthalmologist to changes in visual acuity, elevated extraocular pressure or blood pressure, etc.
Assistant Coordinator, Clinical Research (Part-time) Baylor College of MedicineAssistant Coordinator, Clinical Research (Part-time)Houston, TX$15,660–$18,423 / yearDay to day duties will include contacting research participants for appointment reminders, entering participant information into a database, and assembling documentation for appointments. The Assistant Coordinator will assist Dr. Chadi Calarge's research team by providing administrative support to the research lab.
Assistant Coordinator, Clinical Research Baylor College of MedicineAssistant Coordinator, Clinical ResearchHouston, TX$39,150–$46,059 / yearDay to day duties will include contacting research participants for appointment reminders, entering participant information into a database, and assembling documentation for appointments. The Assistant Coordinator will assist Dr. Chadi Calarge's research team by providing administrative support to the research lab.
NewResearch Assistant I / Abdominal Imaging Department University of Texas MD Anderson Cancer CenterResearch Assistant I / Abdominal Imaging DepartmentHouston, TXRemoteThe Research Assistant I plays a key role in the technical execution of research projects, particularly those focused on machine learning and artificial intelligence applications for abdominal organ segmentation. This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening.
Research Assistant I/II/III - Psychiatry and Behavioral Sciences' Houston Psychosis Research Center UTHealthResearch Assistant I/II/III - Psychiatry and Behavioral Sciences' Houston Psychosis Research CenterHouston, TXFull timePersonnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure. To the extent that a position requires the holder to research, work on, or have access to critical infrastructure as defined in Texas Business and Commerce Code §117.001(2), the ability to maintain the security or integrity of the infrastructure is a minimum qualification to be hired for and to continue to be employed in that position.
Research Assistant I - ALTO UTHealthResearch Assistant I - ALTOHouston, TXFull timeKey responsibilities include recruiting and screening participants, collecting and documenting clinical data, obtaining informed consent, assisting with clinical procedures, managing and analyzing data, ensuring regulatory compliance, coordinating study activities, maintaining participant follow-up, monitoring quality assurance, and reporting adverse events. Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure.
Research Assistant I - Leukemia MD AndersonResearch Assistant I - LeukemiaHouston, TXThe Research Assistant I helps advance leukemia research by supporting critical laboratory functions and ensuring high-quality sample preparation, molecular analysis, and specimen management. The Research Assistant I works within this scientific setting to support laboratory operations, collaborate with research personnel, and facilitate the successful execution of leukemia research projects.
Clinical Research Coordinator IntraCareClinical Research CoordinatorGreenville, TexasApplicants who have worked 2+ years in a pulmonary office and are familiar with patient assessments, spirometry, or chronic respiratory disease management will find this an excellent opportunity to transition into clinical research. Maintain comprehensive and organized study documentation, such as case report forms, regulatory paperwork, and study logs.
Clinical Research Specialist IntraCareClinical Research SpecialistDallas, TexasApplicants who have worked 2+ years in a pulmonary office and are familiar with patient assessments, spirometry, or chronic respiratory disease management will find this an excellent opportunity to transition into clinical research. Maintain comprehensive and organized study documentation, such as case report forms, regulatory paperwork, and study logs.
Clinical Research Assistant Retina Consultants of TexasClinical Research AssistantKaty, TexasFull timeIn addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period: Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire. This position will be responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures.