NewResearch Coordinator III - Pediatrics Pulmonary University of Texas Health Science Center at HoustonResearch Coordinator III - Pediatrics PulmonaryHouston, TXThe Department of Pediatrics aims to: provide the highest quality and cost-efficient medical care to infants, children, and adolescents entrusted to us; advance the knowledge in biomedical, clinical, and behavioral science through our research programs; and provide excellence and innovation in training the next generation of pediatricians and sub-specialists through our medical student, residency, and fellowship programs. Health Services\Certified Clinical Research Professional (CCRP) by Society of Clinical Research Associates (SOCRA) preferredMinimum Education:Bachelor''s Degree in a related field required Master''s Degree preferred May substitute required education with equivalent years of experience beyond the minimum experience requirement.
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.
NewResearch 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.
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.
Manager Clinical Trials Houston Methodist HospitalManager Clinical TrialsHouston, TXImplements complex research projects, including screening and enrolling subjects, and conducting testing procedures required by study protocol (medical history interview, vital signs, collect and enter data into case report forms, reporting to study monitors), prepares presentations and schedules institutional training for physicians, nurses, and staff on research protocol. Houston 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.
Assistant Nurse Manager - Clinical and Translational Research Center University of Texas MD Anderson Cancer CenterAssistant Nurse Manager - Clinical and Translational Research CenterHouston, TX$111,000–$167,000 / yearInformation Requisition ID: 179622 Employment Status: Full-Time Employee Status: Regular Work Week: Days Minimum Salary: US Dollar (USD) 111,000 Midpoint Salary: US Dollar (USD) 139,000 Maximum Salary: US Dollar (USD) 167,000 FLSA: exempt and eligible for overtime, paid at a straight rate Fund Type: Hard Work Location: Onsite Pivotal Position: Yes Referral Bonus Available?: Preferred: Certification in Oncology, American Heart Association Basic Life Support (BLS), ACLS (Advanced Cardiac Life Support) or PALS (Pediatric Advanced Life Support) certification as required by patient care area.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Houston, TexasFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
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, PRN (Preferably Bilingual, Phlebotomist, LVN Or Registered Nurse) Care AccessClinical Research Assistant, PRN (Preferably Bilingual, Phlebotomist, LVN Or Registered Nurse)Houston, TX$19–$44 / 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. 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).
Coordinator Clinical Studies - Gynecologic Oncology University of Texas MD Anderson Cancer CenterCoordinator Clinical Studies - Gynecologic OncologyHouston, TXThis role provides meaningful opportunities to contribute to high-impact multicenter trials, work closely with leading investigators, and grow long-term clinical research skills while maintaining a healthy work-life balance through a hybrid schedule. This Clinical Research Coordinator role supports multidisciplinary clinical teams and investigators in a highly regulated research environment, ensuring protocol integrity, patient safety, and data quality across single-site and multicenter clinical trials.
NewClinical Research Nurse - Transplant Center Houston Methodist HospitalClinical 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. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
Clinical Research Nurse - Neurology / Alzheimer Houston Methodist HospitalClinical Research Nurse - Neurology / AlzheimerHouston, 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. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
Clinical Research Nurse - Medicine Houston Methodist HospitalClinical Research Nurse - MedicineHouston, 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. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
Clinical Trial Manager Heartflow IncClinical Trial ManagerHouston, TXRemote$95,000–$125,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart.
Clinical Research Administrator - Pediatrics TMC University of Texas Health Science Center at HoustonClinical Research Administrator - Pediatrics TMCHouston, TXCertification/Skills: NoneMinimum Education:Bachelor''s Degree in Healthcare Administration, Business, Finance, Accounting, or related degree requiredMinimum Experience:3 years of related experience requiredPhysical Requirements:Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount 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!
Research Coordinator III - Academic Offices of Clinical Trials Houston Methodist HospitalResearch Coordinator III - Academic Offices of Clinical TrialsHouston, 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. At Houston Methodist, the Research Coordinator III position is responsible for coordinating the drive on multiple clinical research projects and/or for multiple Principal Investigators (PI), gathering patient data via methods specified in the study protocol and providing general administrative duties in support of the study.
Travel Clinical Research Assistant Care AccessTravel Clinical Research AssistantHumble, TX$24–$38 / 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. Documentation & Regulatory Compliance: Accurately document study activities in real time, maintain study logs and trackers, request medical records and participant payments, and ensure compliance with FDA regulations, ICH-GCP, study protocols, and Care Access SOPs.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical 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;].
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.
NewCoordinator, Clinical Studies - Experimental Therapeutics University of Texas MD Anderson Cancer CenterCoordinator, Clinical Studies - Experimental TherapeuticsHouston, TXThe Experimental Therapeutics department supports innovative clinical research studies that advance early detection, prevention, and treatment strategies through multidisciplinary collaboration with physicians, research teams, and clinical partners. Experience working independently in a clinical setting, collaborating with physicians, performing phlebotomy, explaining laboratory results and next steps to participants, and coordinating follow-up care is highly desirable.
Director, Clinical Research Regulatory Affairs University of Texas MD Anderson Cancer CenterDirector, Clinical Research Regulatory AffairsHouston, TXRemoteSuccessful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience Completion of both programs can be substituted for a maximum of two years of supervisory or management experience. Preferred: Demonstrated experience preparing and managing INDs and/or IDEs; familiarity with companion diagnostics and combination products is a plus, and an in-depth knowledge of FDA regulations, ICH guidelines, and GCP requirements, and an experience with EMA submissions.
Clinical Research Chart QA/Auditor Advanced Rheumatology of HoustonClinical Research Chart QA/AuditorThe Woodlands, Texas$60–$100We are seeking an experienced Clinical Research Quality Assurance (QA) Auditor with strong FDA audit experience to support ongoing and upcoming clinical research activities. Key Responsibilities: Conduct internal and external audits of clinical trials, vendors, and systems to ensure compliance with FDA regulations, ICH-GCP, and company SOPs.
Clinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorSugar Land, TexasScheduling 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;].
Clinical Research Coordinator - Onsite Advanced Rheumatology of HoustonClinical Research Coordinator - OnsiteThe Woodlands, Texas$40,000–$75,000In this hands-on role, you will help coordinate clinical trials involving autoimmune, inflammatory, and rheumatologic conditions while working closely with patients, investigators, sponsors, and clinical research partners. Join Our Team Become part of a dedicated team committed to conducting high-quality clinical research and improving outcomes for patients living with autoimmune and inflammatory conditions.
Program Manager II, Health Education, Research, Training, Clinical Services & Community Engagement Texas Southern UniversityProgram Manager II, Health Education, Research, Training, Clinical Services & Community EngagementHouston, TX$74,879.81–$95,471.75 / yearJOB SUMMARY: The Program Manager II for Health Education, Research, Training, Clinical Services & Community Engagement leads planning and implementation of health education, research, training, clinical services, and community engagement initiatives that expand access to preventive care, improve health outcomes, and strengthen partnerships across community-based organizations, faith-based organizations, clinics, and public agencies. Posting Number TSU203616 Official TSU Title Program Manager II, Health Education, Research, Training, Clinical Services & Community Engagement Grant Title Program Manager II, Health Education, Research, Training, Clinical Services & Community Engagement Job Description Summary / TWC Summary.
Clinical Research Coordinator 1 Medicine Houston Methodist HospitalClinical Research Coordinator 1 MedicineHouston, 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. Houston Methodist Education Institute coordinates our primary academic affiliation with Weill Cornell Medicine and other joint programs, including the Engineering Medicine Program at Texas A&M University Intercollegiate School of Engineering Medicine.
Clinical Research Physician - Internal Medicine or Metabolic - part time (16 hours per week) Alcanza Clinical Research LLCClinical Research Physician - Internal Medicine or Metabolic - part time (16 hours per week)Sugar Land, TXEnsures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials in adherence with FDA, ICH, NIH, GCPs, & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH, FDA, DAGCP, guidelines, local regulations, study protocol, and company policies and processes.
Postdoctoral Associate - Aortic Imaging & Clinical Research Baylor College of MedicinePostdoctoral Associate - Aortic Imaging & Clinical ResearchHouston, TXParticipates in prospective and retrospective imaging-based and clinical research projects focused on aortic disease and complex endovascular aortic repair, including protocol development, study design, clinical data collection and management, and imaging data organization and analysis. The Postdoctoral Associate will receive training under the guidance of the Principal Investigators and collaborating investigators to conduct prospective or retrospective imaging-based and clinical research projects focused on aortic disease and complex endovascular aortic repairs.
Research Coordinator II - Academic Offices of Clinical Trials Houston Methodist HospitalResearch Coordinator II - Academic Offices of Clinical TrialsHouston, 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.
Assistant Professor, Clinical Faculty Appointment (CFA), Lymphoma-Myeloma University of Texas MD Anderson Cancer CenterAssistant Professor, Clinical Faculty Appointment (CFA), Lymphoma-MyelomaHouston, TXThe selected faculty will provide clinical care to patients, manage care teams for both inpatient and outpatient settings, and provide a teaching environment for fellows, residents, and students in the specialties of Lymphoma/Myeloma. 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.
Assistant Professor, Clinical Faculty (CFA), Lymphoma & Myeloma University of Texas MD Anderson Cancer CenterAssistant Professor, Clinical Faculty (CFA), Lymphoma & MyelomaHouston, TX$287,044–$367,301 / yearIntegrity Behaviors • Reliability: Communicates frequently, honestly and openly • Accountability: Holds self and others accountable for practicing our values • Safety: Notices a safety concern and brings it to someones attention; Models safe behaviors (wears badge, washes hands, keeps work area clean and orderly). Additional Information Requisition ID: 175890 Employee Status: Regular Minimum Salary: US Dollar (USD) 0 Midpoint Salary: US Dollar (USD) 0 Maximum Salary: US Dollar (USD) 0 FLSA: exempt and not eligible for overtime pay Work Location: Onsite Science Jobs: No #LI-Onsite.
Assistant Professor, Clinical Faculty Appointment (CFA) - Lymphoma-Myeloma University of Texas MD Anderson Cancer CenterAssistant Professor, Clinical Faculty Appointment (CFA) - Lymphoma-MyelomaHouston, TXThe selected faculty will provide clinical care to patients, manage care teams for both inpatient and outpatient settings, and provide a teaching environment for fellows, residents, and students in the specialties of Lymphoma. 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.
Open Rank, Clinical Faculty Appointment, Department of Infectious Disease University of Texas MD Anderson Cancer CenterOpen Rank, Clinical Faculty Appointment, Department of Infectious DiseaseHouston, TXIdentify grants and funding sources for research funding, submit grants and protocols in accordance with rules and deadline applications, develop budgets and analyses, and complete grant and protocol application forms. 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.
NewAssistant Professor, Clinical Faculty Appointment, Department of Lymphoma Myeloma University of Texas MD Anderson Cancer CenterAssistant Professor, Clinical Faculty Appointment, Department of Lymphoma MyelomaHouston, TXThe selected faculty will provide clinical care to patients, manage care teams for both inpatient and outpatient settings, and provide a teaching environment for fellows, residents, and students in the specialties of Lymphoma. 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.
Clinical Research Coordinator II - Houston, TX Iterative HealthClinical Research Coordinator II - Houston, TXHouston, TXWe 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.
Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week) Alcanza Clinical ResearchClinical Research Physician - Metabolic or Hepatology - part time (16 hours per week)Sugar Land, TexasEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Coordinator II - Houston, TX Iterative Scopes Inc.Clinical Research Coordinator II - Houston, TXHouston, TXThis role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success. Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
Clinical Trial Laboratory Supervisor MD AndersonClinical Trial Laboratory SupervisorHouston, TXThe ideal candidate for this role brings prior experience managing direct reports and overseeing daily laboratory operations, with strong working knowledge of laboratory environments and specimen handling. The Clinical Trial Laboratory Supervisor also collaborates closely with study sponsors, research partners, and regulatory bodies to resolve complex protocol issues and safeguard protocol integrity.
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).
Travel Clinical Research Assistant Care Access Research LLCTravel Clinical Research AssistantHumble, TX$24–$38 / 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. Documentation & Regulatory Compliance: Accurately document study activities in real time, maintain study logs and trackers, request medical records and participant payments, and ensure compliance with FDA regulations, ICH-GCP, study protocols, and Care Access SOPs.
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.
Research Coordinator III (Clinical Trials) - Neurosurgery University of Texas Health Science Center at HoustonResearch Coordinator III (Clinical Trials) - NeurosurgeryHouston, 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 Fellow 0 Houston Methodist HospitalClinical Research Fellow 0Houston, TXClinical Research Fellow 0 - None Clinical Research Fellow 1 - One year of post-terminal experience Clinical Research Fellow 2 - Two years of post-terminal experience Clinical Research Fellow 3 - Three years of post-terminal experience Clinical Research Fellow 4 - Four years of post-terminal experience. Prepares and delivers educational presentations and deliver written reports of scholarship, including but not limited to, published manuscripts in peer-reviewed journals, quarterly activity reports to fellowship stakeholders, and activity reports to external study sponsors as needed.
Clinical Research Fellow - Dr. Connor Houston Methodist HospitalClinical Research Fellow - Dr. ConnorHouston, TXClinical Research Fellow 0 - None Clinical Research Fellow 1 - One year of post-terminal experience Clinical Research Fellow 2 - Two years of post-terminal experience Clinical Research Fellow 3 - Three years of post-terminal experience Clinical Research Fellow 4 - Four years of post-terminal experience. Prepares and delivers educational presentations and deliver written reports of scholarship, including but not limited to, published manuscripts in peer-reviewed journals, quarterly activity reports to fellowship stakeholders, and activity reports to external study sponsors as needed.
Clinical Research Fellow Houston Methodist HospitalClinical Research FellowHouston, TXClinical Research Fellow 0 - None Clinical Research Fellow 1 - One year of post-terminal experience Clinical Research Fellow 2 - Two years of post-terminal experience Clinical Research Fellow 3 - Three years of post-terminal experience Clinical Research Fellow 4 - Four years of post-terminal experience. Prepares and delivers educational presentations and deliver written reports of scholarship, including but not limited to, published manuscripts in peer-reviewed journals, quarterly activity reports to fellowship stakeholders, and activity reports to external study sponsors as needed.
Clinical Trial Research Coordinator I Houston Methodist HospitalClinical Trial Research Coordinator IHouston, 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. Houston Methodist Education Institute coordinates our primary academic affiliation with Weill Cornell Medicine and other joint programs, including the Engineering Medicine Program at Texas A&M University Intercollegiate School of Engineering Medicine.
Clinical Research Coordinator II - Houston, TX Iterative Scopes IncClinical Research Coordinator II - Houston, TXHouston, TXWe 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.
Clinical Research Site Operations Intern aQua DialysisClinical Research Site Operations InternHouston, TXTemporaryAqua Research Institute LLC, in partnership with Boson Health, is proud to launch a structured summer internship program designed to provide foreign medical graduates, master's students in clinical research, and transitioning professionals with a comprehensive, real-world learning experience in clinical trial site operations. Interns will gain first-hand exposure to the daily workings of a high-performing research site and mentorship from experienced leaders in the field.
Clinical Investigation Technician (Certified Phlebotomist) - Breast Medical Oncology MD AndersonClinical Investigation Technician (Certified Phlebotomist) - Breast Medical OncologyHouston, TXCoordinates departmental efforts to identify potential patients in the clinics and on the in-patient floors: • Draw blood samples and retrieve lab and/or tissue samples from Diagnostic Laboratory and other hospital locations as required per protocol. This department seeks to improve the survival of breast cancer patients, provide new knowledge through research, patient-centered clinical care, cancer prevention, and education and outreach with the ultimate goal of eliminating breast cancer.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedTX$71,900–$189,000 / yearEnsure 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.