Clinical Research Specialist (Neurology Department) Houston Methodist HospitalClinical Research Specialist (Neurology Department)Houston, 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 Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols, gathering patient data via methods specified in the study protocol, study reports.
Clinical Research Coordinator II - Nurse Iterative Scopes IncClinical Research Coordinator II - NurseWebster, TXBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
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.
Senior Clinical Research Associate (Texas Region) Axsome TherapeuticsSenior Clinical Research Associate (Texas Region)Houston, TXOur industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, agitation associated with dementia due to Alzheimer's disease, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, as well as multiple novel product candidates addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Reporting to the Senior Manager of Clinical Monitoring, theSenior CRA will be responsible for site management and monitoring activities at assigned sites across assigned programs ensuring the trial is conducted in compliance with the protocol, ICH/GCP, applicable regulatory requirements and applicable SOPs/Work Instructions.
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;].
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 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!
Clinical 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.
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 Documentation Specialist (Remote -Texas Resident) - Clinical Data University of Texas Medical Branch at GalvestonClinical Documentation Specialist (Remote -Texas Resident) - Clinical DataGalveston, TXRemote$71,923–$115,077 / yearRegistered nurse (or medical school graduate) with a minimum of 3 years inpatient clinical experience, advanced clinical expertise and an extensive knowledge of complex disease processes with broad clinical experience in an inpatient setting. Minimum Qualifications: Certified Registered Health Information Administrator (RHIA), Technician (RHIT), or an associate degree in a healthcare-related discipline with Certified Coding Specialist (CCS) certification, and a minimum of 3 years of medical coding experience.
Clinical Research Nurse Houston Methodist HospitalClinical 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. 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.
NewClinical Research Coordinator I Care AccessClinical Research Coordinator IHouston, 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 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 Coordinator II - Neurology Alzheimer Houston Methodist HospitalClinical Research Coordinator II - 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. 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.
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.
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.
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.
Clinical Research Site Operations Intern aQua DialysisClinical Research Site Operations InternHouston, TXTemporarySUMMER INTERNSHIP OPPORTUNITYAQUA RESEARCH INSTITUTE LLC / BOSON HEALTHEmpowering the Next Generation of Clinical Researchers Internship Title: Clinical Research Site Operations InternLocation: Aqua Research Institute, [Insert City, State]Duration: 8 WeeksType: Unpaid InternshipSpots Available: 4Commitment: 20-30 hours/week (in-person strongly preferred) ABOUT THE PROGRAMAqua 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.
NewClinical Research Coordinator Forefront DermatologyClinical Research CoordinatorHouston, TexasFull timeEngages directly with research participants and exercises independent judgment in identifying risks and implementing strategies that impact study success and organizational research objectives across sites. Drive participant recruitment strategy, optimize screening and enrollment workflows, and meet study performance targets while ensuring positive participant experience and retention.
NewDirector, Clinical Research Regulatory Affairs University of Texas MD Anderson Cancer CenterDirector, Clinical Research Regulatory AffairsHouston, TXRemotePreferred: 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, FDA submissions, ICH guidelines, and GCP requirements, and an experience with EMA submissions. The ideal candidate brings a preferred Master's degree in a life sciences, pharmacy, medicine, or related field, along with extensive experience in oncology regulatory affairs, including IND and IDE submissions, FDA interactions, FDA submissions and EMA exposure.