Research Scientist I - Physical Therapy and Rehab Science UTMB HealthResearch Scientist I - Physical Therapy and Rehab ScienceGalveston, TXBachelor's or Master's degree in engineering (electrical, biomedical, mechanical, computer, or related field) and experience with instrumentation, embedded systems, or research-grade hardware, proficiency in software development and data analysis pipelines, and ability to support laboratory operations across multiple active research programs. The responsibilities include instrumented laboratory environment support hardware and software engineering for specialized measurement equipment data analysis pipeline development (including AI/ML applications) device configuration and troubleshooting and systems documentation.
Research Intern - Melanoma Medical Oncology - Research MD AndersonResearch Intern - Melanoma Medical Oncology - ResearchHouston, TXLearn how to evaluate responses to systemic treatments in melanoma using radiographic and pathological findings, as well as biological, clinical, and host-related determinants of differential therapeutic responses. Perform literature review on determinants of benefit from systemic therapeutics in melanoma, including patient and disease characteristics, comorbidities, concomitant medications and other host factors such as lifestyle and microbiome.
Clinical Research Assistant/ Medical Assistant Alcanza Clinical ResearchClinical Research Assistant/ Medical AssistantKaty, TexasResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; 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; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Research Medical Laboratory Scientist MD AndersonResearch Medical Laboratory ScientistHouston, TXThe primary purpose of the Research Medical Laboratory Scientist position is to independently perform procedures using clinical and translational research methodologies (PK, PD, PG, PBMC, etc.) and assist in the development of new laboratory services for the CTLS Laboratory. Responsible for multidisciplinary teamwork involving maintenance of quality control and equipment utilized for the production of analytical data on patient specimens affecting clinical trials.
NewCoordinator, Research Data - GI Medical Oncology University of Texas MD Anderson Cancer CenterCoordinator, Research Data - GI Medical OncologyHouston, TXThe Research Data Coordinator works closely with investigators, research staff, clinicians, patients, sponsors, and collaborators to ensure accurate research records, efficient workflows, and successful execution of research initiatives. The ideal candidate will have experience supporting clinical research activities, research data management, biospecimen collection and tracking, quality control processes, and patient coordination.
NewPostdoctoral Fellow - GI Medical Oncology - Research University of Texas MD Anderson Cancer CenterPostdoctoral Fellow - GI Medical Oncology - ResearchHouston, TX$64,000–$76,000 / yearThis 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. The role includes planning training and research activities for assigned laboratory and research personnel, supervising the use of laboratory equipment, and implementing laboratory safety procedures.
Research Assistant II - GI Medical Oncology MD AndersonResearch Assistant II - GI Medical OncologyHouston, TXPerform basic to intermediate molecular biology techniques such as DNA, RNA and protein extraction and measurement, DNA, RNA and protein gel electrophoresis, real-time quantitative RT-PCR, recombinant DNA cloning (transformation and mutagenesis). 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.
NewResearch Assistant II - GI Medical Oncology University of Texas MD Anderson Cancer CenterResearch Assistant II - GI Medical OncologyHouston, TXThe University of Texas MD Anderson Cancer Center is dedicated to eliminating cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and education for undergraduate and graduate students, trainees, professionals, employees, and the public. The Research Assistant II position within Gastrointestinal Medical Oncology supports translational cancer research focused on intestinal adenocarcinomas, colorectal cancer biology, patient-derived xenograft models, treatment response and resistance mechanisms, and tumor immunology.
Instructor, Research Faculty Appointment (RFA) - GI Medical Oncology MD AndersonInstructor, Research Faculty Appointment (RFA) - GI Medical OncologyHouston, TXParticipate in scientific meetings, divisional and departmental seminars/Grand Rounds and other research related activities as necessary to present results of experiments and make ready results for publications of manuscripts/abstracts. Visually review, understand, synthesize, interpolate, summarize or provide editorial commentary on manuscripts, grant applications, research literature, or professional communications, verbally or by use of electronic and manual methods.
Clinical Research Associate (Cra) - Cardiovascular/Vaccine/Infectious Disease- Remote Merck & Co., Inc.Clinical Research Associate (Cra) - Cardiovascular/Vaccine/Infectious Disease- RemoteHouston, TXRemote$96,200–$151,400 / yearRequired Skills: Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies, Data Analysis, Data Reporting, Early Clinical Development, Policy Development, Preventive Action, Protocol Adherence, Regulatory Compliance, Site Management. Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Clinical Research Coordinator - Onsite - North Houston Advanced Rheumatology of HoustonClinical Research Coordinator - Onsite - North HoustonThe Woodlands, Texas$50,000–$85,000In 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. Our growing private rheumatology practice in The Woodlands, Texas, is seeking a motivated and highly organized Clinical Research Coordinator (CRC) to join our research team.
Clinical Research Coordinator aQua DialysisClinical Research CoordinatorHouston, TXFull timeConcrete background in medicine· Thorough knowledge of medical research· Excellent verbal and written communication skills· Proficiency with computers, especially Microsoft office· Knowledgeable about ICH Guidelines, GCPs, as well as FDA regulations· Able to handle multiple protocols in various therapeutic areas· Must be detailed oriented· Must be willing to travel to various locations in Greater Houston Education Experience· Bachelors required, Master degree preferred.· Maintains strict patient confidentiality according to HIPAA regulations and applicable law.· Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs guidelines· Contribute to growth of company with future supervisory role REQUIREMENTS:· Great at customer service· Self-motivated/starter· Outgoing, excellent recruiting skills· Phlebotomy experiences a MUST.·
Clinical Trial Research Assistant Advanced Rheumatology of HoustonClinical Trial Research AssistantThe Woodlands, Texas$15–$18Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. Preferred Skills: Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
NewBilingual Clinical Research Coordinator Actalent IncBilingual Clinical Research CoordinatorRichmond, TX$25–$35 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. You will work onsite at a clinical research facility in the Richmond/Houston, TX area, collaborating closely with a multidisciplinary research team and interacting regularly with study participants.
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 Alcanza Clinical Research LLCClinical Research CoordinatorKaty, 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;].
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.
NewClinical Research Coordinator (CRC) LINQ Research, LLCClinical Research Coordinator (CRC)Pearland, TXThis position is ideal for a CRC who has previously taken ownership of clinical studies, interfaced directly with study monitors and sponsors, and can confidently manage patient visits, data integrity, investigational product accountability, and study activities with minimal oversight. The CRC will work closely with the Site Manager, Principal Investigator, Investigators, Recruitment, Regulatory, sponsors, CROs, and study monitors and will serve as a primary point of contact for study participants, sponsors, and monitors.
Clinical Research Systems Manager MD AndersonClinical Research Systems ManagerHouston, TXRemoteThe Clinical Research Systems Manager ensures ensures the integrity, availability, and appropriate use of CTMS data across the clinical trial lifecycle while leading complex technical projects that advance research efficiency, compliance, and reporting capabilities. The position offers opportunities to lead complex technical initiatives, collaborate with research and technology experts, and shape infrastructure that supports institutional growth, professional development, and work-life balance.
Clinical 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;].