Clinical Research Associate (CRA) Dallas Medpace Holdings IncClinical Research Associate (CRA) DallasHouston, TXp>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 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; 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; 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; and Must be detail-oriented and efficient in time management.
X-Ray Technologist – Float Position {170226} A-Line Staffing Solutions LLCX-Ray Technologist – Float Position {170226}Houston, TX$29–$35 / hourThis is an excellent opportunity for both experienced technologists and recent graduates looking to grow their careers in a dynamic healthcare environment. Technologists will be assigned to one site per day, with schedules communicated in advance to support work-life balance and planning.
Manager, Clinical Research - Pediatrics - Center for Research Advancement Administration Baylor College of MedicineManager, Clinical Research - Pediatrics - Center for Research Advancement AdministrationHouston, TX$99,213–$116,721 / yearCertification as a Clinical Research Professional (CRP) or Clinical Research Coordinator (CRC) from the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP). Responsible for overseeing and directing the day-to-day clinical research operations of the Neurology research team within the Center for Research Advancement (CRA), Department of Pediatrics.
Senior Quality Assurance and Control Associate - Clinical Research Baylor College of MedicineSenior Quality Assurance and Control Associate - Clinical ResearchHouston, TX$79,092–$93,000 / yearThis role leads and supports internal audits, sponsor audits, and regulatory inspections, including FDA inspections, and ensures the accuracy, completeness, and integrity of clinical study documentation and processes. The Senior Quality Assurance and Control Associate provides independent quality oversight of clinical research activities to ensure compliance with FDA regulations, ICH-Good Clinical Practice (ICH-GCP), sponsor requirements, and institutional policies.
Lead Clinical Research Associate ICON PlcLead Clinical Research AssociateHouston, TXCollaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials. You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.
Clinical Research Associate ICON PlcClinical Research AssociateHouston, TXFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
Senior Clinical Research Associate ImmaticsSenior Clinical Research AssociateHouston, TexasRemoteIn this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateTXRemoteli>Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Senior Research Coordinator - Clinical Research Baylor College of MedicineSenior Research Coordinator - Clinical ResearchHouston, TX$70,618–$83,080 / yearThis role is essential for coordination of the OCR research portfolio, liaising with PIs, regulatory staff, sponsor representatives, investigational pharmacy, and provides cross-coverage across the OCR team. Coordinates research protocol procedures and processes, working closely with Research Manager, study team, and OCR Regulatory team on monitoring visit report findings.
Senior Research Administration Associate - Clinical Trial Billing and Finance Baylor College of MedicineSenior Research Administration Associate - Clinical Trial Billing and FinanceHouston, TX$79,092–$93,000 / yearThe Senior Research Administration Associate - Clinical Trial Billing and Finance is a pivotal role responsible for managing the financial lifecycle of industry sponsored clinical trials in the Center of Research Advancement for the Departments of Pediatrics and other supported TCH Departments. Participate in study feasibility and related meetings, providing expertise in budgeting and financial management to ensure accurate cost projections and compliance with institutional and sponsor requirements.
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.
Senior Clinical Research Associate Immatics NVSenior Clinical Research AssociateHouston, TXRemote$120,000–$135,000 / yearIn this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.
Senior Clinical Research Associate IRESenior Clinical Research AssociateHouston, TexasAs a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Supervisor, Clinical Research - Surgery - Core Research Baylor College of MedicineSupervisor, Clinical Research - Surgery - Core ResearchHouston, TX$70,618–$83,080 / yearOversee the daily operations of clinical research studies and research staff to ensure studies are conducted according to protocol, regulatory requirements, institutional policies, and sponsor expectations. Based on departmental needs, flexibility is important, as occasional early morning, evening, or weekend hours may be required to support study visits, sponsor meetings, or research deadlines.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedTXp>• Ensure 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.
Clinical Research Associate (CRA) Healing Kidneys Institute Of HoustoClinical Research Associate (CRA)Conroe, TXHealing Kidneys Clinical Research is a Nephrology clinical trials focused company in Rare disease space that uses proprietary technology to: Increase patient access to research trials within our communities, Deliver superior clinical research enrollment metrics to Pharma sponsors. Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies.
Coordinator, Clinical Studies - Radiation Oncology Clinical Research Department University of Texas MD Anderson Cancer CenterCoordinator, Clinical Studies - Radiation Oncology Clinical Research DepartmentHouston, TXp>The University of Texas MD Anderson Cancer Center is recruiting a Clinical Studies Coordinator to support the Radiation Oncology department, which delivers advanced, multidisciplinary cancer treatment and conducts innovative clinical trials to improve patient outcomes. As a Clinical Studies Coordinator, you will play a meaningful part in improving patient outcomes, developing your clinical research expertise, and building a rewarding career in a collaborative and mission-driven environment that values professional growth and work-life balance.
NewPostdoctoral Associate - Aortic Imaging & Clinical Research Baylor College of MedicinePostdoctoral Associate - Aortic Imaging & Clinical ResearchHouston, TXul>Participates 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.
NewAssistant Clinical Research Coordinator Profound ResearchAssistant Clinical Research CoordinatorPasadena, 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 .
Senior Clinical Research Associate, Early Clinical Development IQVIA Holdings IncSenior Clinical Research Associate, Early Clinical DevelopmentHouston, TXb>Deprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85. .
Senior Data Analytics Associate - Clinical Research Data Baylor College of MedicineSenior Data Analytics Associate - Clinical Research DataHouston, TX$79,092–$93,049 / yearThis role is responsible for maintaining and optimizing research databases, sustaining established Power BI dashboards, and developing new data-driven solutions that support complex fetal intervention research, including FDA regulated clinical trials. The analyst will apply advanced analytical methods, statistical modeling, and data visualization techniques to drive evidence-based decision making, ensure data integrity, and enhance operational and research outcomes across interdepartmental clinical research initiatives.
Clinical Research Assistant, PRN (Preferably Bilingual, Phlebotomist, LVN or Registered Nurse) Care AccessClinical Research Assistant, PRN (Preferably Bilingual, Phlebotomist, LVN or Registered Nurse)Houston, Texasp>With 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).
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.
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.
Clinical Research Coordinator I Ora IncClinical Research Coordinator IHouston, TXPerform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
Clinical Research Assistant Care AccessClinical Research AssistantHouston, TX$19–$33 / hourp>With 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. Certifications/Licenses, Education, and Experience:A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
NewSr. 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.
Sr. Clinical Research Nurse Houston Methodist HospitalSr. Clinical Research NurseHouston, 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.
Community Clinical Research Educator Intern Care Access Research LLCCommunity Clinical Research Educator InternHouston, TXWith 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. We are looking for a Community Clinical Research Educator Intern who is deeply passionate about promoting awareness and education of clinical research, and access to clinical trials., to diverse communities.
Community Education, Health Services, and Clinical Research Nurse Texas Southern UniversityCommunity Education, Health Services, and Clinical Research NurseHouston, TX$80,870.19–$103,109.49 / yearPreferred: Certified Health Education Specialist, CHES; Certified in Public Health, CPH; Community Health Worker, CHW; Certified Clinical Research Professional, CCRP or eligible and intent to become certified; CITI GCP, Human Subjects credentialing and knowledge of regulatory requirements. The Community Education Health Services and Clinical Research Nurse at Texas Southern University will play a vital role in improving community health outcomes through community education as well as development and implementation of preventive health services and clinical research activities.
Clinical Research Coordinator II Care Access Research LLCClinical Research Coordinator IIHouston, TX$60,000–$90,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Clinical Research Assistant Bilingual in Spanish Care Access Research LLCClinical Research Assistant Bilingual in SpanishHouston, TX$19–$33 / hourp>With 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 Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorSugar Land, TXli>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. 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 and Health - Clin Research Nurse II AES MindlanceClinical and Health - Clin Research Nurse II AESHouston, TXLogs/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.).
Supervisor, Clinical Research - Medicine (On-site) Baylor College of MedicineSupervisor, Clinical Research - Medicine (On-site)Houston, TX$70,618–$83,080 / yearThe Clinical Research Supervisor for the Section of Epidemiology at Baylor College of Medicine will oversee the daily operations of clinical research studies, ensuring compliance with protocols and regulatory requirements. Oversees the daily operational execution of clinical research studies, ensures adherence to study protocols, institutional policies, and regulatory requirements.
Clinical Research Coordinator II Bilingual Spanish Care Access Research LLCClinical Research Coordinator II Bilingual SpanishHouston, TX$60,000–$90,000 / yearStrong organizational, prioritization and leadership skills and capabilities with a strong attention to detail Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel. Excellent working knowledge of medical and research terminology Excellent working knowledge of federal regulations, good clinical practices (GCP) Operates independently for most study activities; escalates complex issues as needed.
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 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.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIAHouston, TXDeprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85.
Senior Clinical Research Coordinator HCA HealthcareSenior Clinical Research CoordinatorHouston, TXThe Senior Clinical Research Coordinator is responsible for coordinating multiple research protocols; serving as a liaison with local investigators and research personnel; and acting as a central resource for assigned research projects. · Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.) .
Regulatory Affairs Associate - Clinical Research Baylor College of MedicineRegulatory Affairs Associate - Clinical ResearchHouston, TX$70,618–$83,080 / yearKnowledge and understanding of clinical research compliance, including OHRP, FDA and other federal regulations and requirements regarding human subjects research, including but not limited to GCPs and related ICH guidelines, informed consent, adverse event reporting and monitoring, and other human subjects research protection requirements. Acts as a liaison between institutional review committees, regulatory agencies and the investigators to ensure that protocols obtain applicable approvals, that protocol amendments are submitted appropriately and that annual renewals are obtained.
Clinical Research Administrator - Pediatrics TMC University of Texas Health Science Center at HoustonClinical Research Administrator - Pediatrics TMCHouston, TXfor description go to https://careers.uth.tmc.edu/us/en/job/UHHUHHUS2600012PEXTERNALENUS/Clinical-Research-Administrator---Pediatrics-TMC.
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.
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 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.
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 Engagement Lead (CREL) - Central Region (Houston, TX) Genentech IncClinical Research Engagement Lead (CREL) - Central Region (Houston, TX)Houston, TX$108,000–$202,000 / yearRelationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).
NewPer Diem Nurse - Clinical & Translational Research Center University of Texas MD Anderson Cancer CenterPer Diem 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. CTRC Job Specific Competencies: The CTRC nurse has the competence and competencies regarding all aspects of administering and monitoring a variety of systemic cancer therapies and other injectable infusions to an adult population in the Clinical & Translation Research Center.
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.