203 Results for

Winter Research Jobs in Texas

Jobs

Irving, TX30+ days ago

Remote

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 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 Experience as a Clinical Research Coordinator (minimum 1 year) 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 Must be detail-oriented and efficient in time management.

Irving (Dallas), Texas30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Houston, TX30+ days ago

$34–$44 Per Hour

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).

Houston, TX30+ days ago

$34–$44 Per Hour

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. As 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.

Tyler, TX30+ days ago

$19–$33 Per Hour

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.

Houston, TX30+ days ago

$19–$33 Per Hour

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 Assistantis 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.

New!

Lubbock, TX2 days ago

$48,000–$63,700 Per Year

Davis College includes the departments of Agricultural and Applied Economics, Agricultural Education and Communications, Animal and Food Sciences, Landscape Architecture, Natural Resources Management, Plant and Soil Science, and Veterinary Sciences along with multiple research centers and institutes. Experience and laboratory skills in dealing with analytical laboratory sample preparation and equipment operation, including microwave digestions, ICP-OES/MS, XRF, GC, IC, CNS analysis, or electrochemical techniques.

Round Rock, TX30+ days ago

$18–$24 Per Hour

Physical requirements: Frequent standing and sitting, ability to view patient images and operate imaging devices, frequent use of a computer terminal, near constant standing and walking, manual dexterity to operate ophthalmic equipment, lifting heavy equipment . Assist research coordinators with providing care for study patients during study visits as well as perform diagnostic testing, schedule their appointments and educate them regarding their retinal condition, available treatment options and details of each study protocol.

Richardson, TX30+ days ago

Other Qualifications To the extent this position requires the holder to research work on or have access to critical infrastructure as defined in Section 117.0012 of the Texas Business and Commerce Code, the ability to maintain the security or integrity of the critical infrastructure is a minimum qualification to be hired and to continue to be employed in the position. Special Instructions Summary Important Message 1: All employees serve as a representative of the University and are expected to display respect, civility, professional courtesy, consideration of others, and discretion in all interactions with members of the UT Dallas community and the general public.

San Antonio, TX30+ days ago

$24–$38 Per Hour

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 Travel 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.

San Marcos, TX30+ days ago

Assist research coordinators to provide care for study patients, during visits, perform diagnostic testing, schedule appointments and educate patients regarding retinal condition, available treatment options and details of study protocol. Performs required trainings and obtains applicable certifications necessary to participate in specific study protocols including GCP, IATA, and other protocol-specific training.

Fort Worth, TX30+ days ago

Title: Research Assistant II (Outreach) Employee Classification: Research Assistant II Campus: University of North Texas - Health Science Center Division: HSC-Div of Rsrch & Innovation SubDivision-Department: HSC-Health Institutes & Centers Department: HSC-Inst Translational Research-304700 Job Location: Fort Worth Salary: Commensurate with Experience FTE: 1.000000 Retirement Eligibility: TRS Eligible. Department Summary The Institute for Translational Research is devoted to bringing novel diagnostics and interventions to patients and families suffering from neurodegenerative diseases, fostering translational research in neurodegenerative diseases at UNTHSC, and Create solutions for a healthier community.

Dallas, TX27 days ago

Texas Retina Associates is Texas’ largest, most experienced ophthalmology practice focused specifically on the diagnosis, medical and surgical management of diseases of the retina and vitreous. Present patient history summary and alert Ophthalmologist to changes in visual acuity, elevated extraocular pressure or blood pressure, etc.

Irving, TX30+ days ago

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; 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. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

Mansfield, TX30+ days ago

PRIME CLINICAL RESEARCH INC has been at the forefront of clinical research in DFW Area, dedicated to delivering high-quality results for our clients. Join PRIME CLINICAL RESEARCH INC as a Clinical Research Coordinator in Mansfield, TX, where you'll play a vital role in advancing medical research.

San Antonio, TX30+ days ago

Full-time

Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. (Including but not limited to: Form FDA 1572, financial disclosures, laboratory certifications, protocol, investigator brochure, institutional review board (IRB) related documents, IND reports delegation of authority (DOA), study specific enrollment logs, monitoring reports, with assistance as needed.

Houston, TX30+ days ago

The Research Assistant I helps advance leukemia research by supporting critical laboratory functions and ensuring high-quality sample preparation, molecular analysis, and specimen management. The Research Assistant I works within this scientific setting to support laboratory operations, collaborate with research personnel, and facilitate the successful execution of leukemia research projects.

San Antonio, Texas14 days ago

About Pinnacle Clinical Research:Pinnacle Clinical Research Network provides world-class clinical trial solutions to its member sites, sponsors, CROs, researchers and patients to accelerate the results of their trials. Complete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs.

Houston, TX30+ days ago

$60,000–$90,000 Per Year

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 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.

Houston, TX30+ days ago

$65,000–$95,000 Per Year

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 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.

Tyler, TX30+ days ago

$60,000–$90,000 Per Year

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 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.

Irving (Dallas), Texas30+ days ago

Responsibilities : 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; 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. Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Conroe, TX24 days ago

Healing 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.

Houston, TX30+ days ago

Some background in molecular biology (PCR, RT-qPCR, Western blot, RNAseq, scRNAseq, IHC) with experience and/or interest in translational research, regenerative medicine, enteric nervous system, neurogastroenterology, intestinal biology, gastroenterology, developmental biology, and/or tissue-engineering. We leverage human pluripotent stem cells (hPSCs) to generate human intestinal organoids (HIOs) for both in vitro and in vivo models, investigating critical aspects of enteric nervous system development and developing cell-based therapies for enteric neuropathies.

Dallas, Texas23 days ago

Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely . Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.

New!

Houston, TX1 day ago

$70,618–$83,080 Per Year

Knowledge 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.

New!

Dallas, TX1 day ago

Remote

$105,000–$118,000 Per Year

Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.

Bellaire30+ days ago

In addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period: Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire. Overview: Retina Consultants of Texas (RCTX) is seeking a Bilingual (Spanish-speaking) Research Assistant to join our innovative team with the mission of Fighting Blindness For The World To See.

San Antonio, Texas30+ days ago

In addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period: Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire. This position will be responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures.

Houston, TX30+ days ago

Full-time

Key responsibilities include recruiting and screening participants, collecting and documenting clinical data, obtaining informed consent, assisting with clinical procedures, managing and analyzing data, ensuring regulatory compliance, coordinating study activities, maintaining participant follow-up, monitoring quality assurance, and reporting adverse events. Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure.

galveston, TX30+ days ago

The Moody Brain Health Institute at UTMB is seeking an outstanding candidate for a tenure/non-tenure-track Assistant/Associate/Full Professor position, appointed in the Department of Internal Medicine specializing in Neurotechnology/Neuroengineering. Collaborate with faculty and research teams across disciplines, such as neurobiology, computational neuroscience, and biomedical engineering, to create groundbreaking neurotechnological innovations with real-world applications.

Houston, TX30+ days ago

The Research Assistant II for Leukemia plays an essential role in maintaining rodent colonies, executing molecular assays, and ensuring high-quality laboratory operations across in vivo and molecular research teams. The ideal candidate has experience with rodent handling, in vivo dosing techniques, molecular biology procedures, and laboratory equipment maintenance, supported by relevant scientific education and familiarity with regulated laboratory environments.

Houston, TX30+ days ago

The ideal candidate for the Research Assistant II brings preferred hands-on mouse breeding and handling experience, skills in mammalian cell culture, and familiarity with techniques such as immunohistochemistry or RNAscope, along with strong organizational and laboratory support capabilities. The position offers opportunities to develop specialized technical skills, collaborate with experienced researchers, and support meaningful scientific progress while maintaining a balanced, supportive work environment.

Houston, TX30+ days ago

Complete training and certification for safe, humane handling of live mice • Maintain mouse colonies and breeding pairs for targeted strains • Set up breeding cages, transfer cages, perform ear tagging and tail snipping, and update colony, breeding, and genotyping records • Implant orthotopic and subcutaneous tumors in mouse models • Perform oral gavage and tail vein injections • Work safely within a BSL2 environment • Monitor mouse health and tumor progression during treatment trials • Conduct in vivo tumor growth and treatment assays • Calculate molarity and prepare accurate media solutions and reagents • Handle acids, polyacrylamide, flammable materials, and biohazards according to OSHA and institutional guidelines • Coordinate weekend or holiday support to maintain continuity of mouse experiments. • Maintain and establish tissue culture cell lines using sterile technique • Determine cell counts and cell viability using microscope and hemocytometer • Monitor, order, and stock tissue culture supplies • Establish short-term cell cultures from human or mouse tissues • Perform basic microbiology, immunology, and in vitro cell growth and proliferation assays.

Tyler, TX30+ days ago

$50,000–$80,000 Per Year

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. We are looking for a Community Clinical Research Educator who is deeply passionate about promoting awareness and education of clinical research, and access to clinical trials., to diverse communities.

Houston, TX20 days ago

Contractor

Knowledge, Skills and Abilities: Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.) Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving Demonstrated ability to exercise discretion and sound judgement Good decision-making, negotiation and influencing skills Good communication skills and English fluency will be an advantage Good organizational skills Good proficiency in basic computer applications Good interpersonal skills to work in a team environment Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification in the clinical / medical field Must hold a valid nursing license (RN, LVN, LPN) within the country operating.

Houston, TX30+ days ago

Full-time

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. To the extent that a position requires the holder to research, work on, or have access to critical infrastructure as defined in Texas Business and Commerce Code §117.001(2), the ability to maintain the security or integrity of the infrastructure is a minimum qualification to be hired for and to continue to be employed in that position.

houston, TX30+ days ago

The selected candidate will serve as Director of the Center for Craniofacial Research (CCR), a university-wide research center that integrates basic, translational, and clinical research in oral and craniofacial biology with members in both the School of Dentistry and the School of Medicine, primarily within the Department of Pediatrics. The School of Dentistry, currently ranked number eight in research funding among U.S. dental schools by the NIDCR, is one of seven schools in UTHealth Houston, which is located in the Texas Medical Center (TMC), the world''''s largest medical complex.

San Antonio, TX30+ days ago

Full-time

Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, CRCs, other members of the research team, Study Sponsor/CROs, potential subjects, and referral sources.

Houston, TX30+ days ago

Perform 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.

Houston, TX30+ days ago

They should be skilled in maintaining cancer cell lines using sterile techniques, familiar with safety procedures for patient samples, and knowledgeable in molecular biology and advanced immunology methods. 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.

Houston, TX30+ days ago

SKILLS AND ABILITIES • Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through ongoing skills, competency assessments, and performance evaluations • Sufficient proficiency in speaking, reading and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security • Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus, and application of positive language principles • Ability to work independently • Capable of handling challenging/difficult situations • Demonstrates sound judgment and executes analytical skills. 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.

New!

Houston, TX1 day ago

$79,092–$93,049 Per Year

This 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.

Houston, TX30+ days ago

Full-time

Fort Worth, Texas30+ days ago

The Institute for Translational Research is devoted to bringing novel diagnostics and interventions to patients and families suffering from neurodegenerative diseases, fostering translational research in neurodegenerative diseases at UNTHSC, and Create solutions for a healthier community. This position will manage community recruitment and participant screening, perform data scoring and quality control, schedule appointments, and handle essential administrative tasks to ensure our clinical trials run smoothly and efficiently.

Mansfield, TX8 days ago

$45,000–$55,000 Per Year

Prime Clinical Research is seeking a Clinical Research Coordinator (without Regulatory) experience to support the operational execution of clinical trials. This position does not include regulatory documentation responsibilities and focuses on the operational coordination of clinical trial visits and participant management.

DeSoto, TX30+ days ago

$45,760–$56,160 Per Year

Support investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring compliance with protocol and site SOPs. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.

DeSoto, TX30+ days ago

$45,760–$56,160 Per Year

Houston, TX30+ days ago

$49,400–$56,200 Per Year

Additional Responsibilities/Duties: • Designs, conducts and analyzes research large experiments or research projects • May liase with other areas of specialization • Personally conducts important and/or technically complex investigations • Operates with considerable independence, provides direction and supervision to graduate or undergraduate students. Provides expertise in the design, operation and analysis of experiments or research projects in areas such as chemistry, biology, psychology, sociology, mathematics, statistics, computer science, physics, optometry, all fields of engineering, etc.

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Winter Research Jobs in Texas

Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings Inc

Clinical Research Associate (CRA) - Dallas Medpace, Inc.

Clinical Research Assistant, PRN Care Access

Clinical Research Assistant, PRN (Bilingual, Registered Nurse) Care Access

Clinical Research Assistant (Bilingual Spanish) Care Access

Clinical Research Assistant (Must be Bilingual) Care Access

TTU Post Doctoral Research Associate in Environmental Soil Chemistry Texas Tech University

Clinical Research Assistant (Round Rock) Austin Retina Associates

Postdoctoral Research Associate University of Texas at Dallas

Travel Clinical Research Assistant Care Access

San Marcos-Clinical Research Assistant Austin Retina Associates

Research Assistant II (Outreach) UNIVERSITY OF NORTH TEXAS SYSTEM

Clinical Research Coordinator / Ophthalmic exp. required - Dallas Texas Retina Associates

Clinical Research Associate PhD in Life Sciences Medpace Holdings Inc

Clinical Research Coordinator PRIME CLINICAL RESEARCH INC

Clinical Research Coordinator U.S. Renal Care, Inc.

Research Assistant I - Leukemia MD Anderson

Clinical Research Coordinator Pinnacle Clinical Research

Clinical Research Coordinator II (Bilingual Spanish) Care Access

Clinical Research Coordinator III (Bilingual in Spanish) Care Access

Clinical Research Coordinator II (Must be Bilingual) Care Access

Clinical Research Associate - PhD in Life Sciences Medpace, Inc.

Clinical Research Associate (CRA) Healing Kidneys Institute Of Housto

Research Assistant II/III - Pediatric Surgery lab University of Texas Health Science Center at Houston

Senior Clinical Research Coordinator Velocity Clinical Research, Inc.

Regulatory Affairs Associate - Clinical Research Baylor College of Medicine

Clinical Research Associate II, Phase I Fortrea Inc

Bilingual Clinical Research Assistant (Spanish) Retina Consultants of Texas

Clinical Research Assistant Retina Consultants of Texas

Research Assistant I - ALTO UTHealth

Assistant Professor of Research - Internal Medicine - MBHI Neuro Technology - Faculty University of Texas Medical Branch at Galveston

Research Assistant II - Leukemia MD Anderson

Research Assistant II MD Anderson

Research Assistant II University of Texas MD Anderson Cancer Center

Community Clinical Research Educator I Care Access

Clinical Research Nurse II AES Integrated Resources, Inc

Research Assistant I/II - Psychiatry and Behavioral Sciences' PIRL-M UTHealth

Director, Center for Craniofacial Research (Associate/Full Professor) - School of Dentistry University of Texas Health Science Center at Houston

Clinical Research Coordinator Assistant (CRCA) Flourish Research

Research Assistant II - GI Medical Oncology MD Anderson

Senior Research Assistant - Experimental Therapeutics MD Anderson

Research Associate - Urology, Gong lab Houston Methodist Hospital

Senior Data Analytics Associate - Clinical Research Data Baylor College of Medicine

Research Assistant II - Pediatric Surgery lab UTHealth

Research Assistant II (Outreach) University of North Texas System

Clinical Research Coordinator (without Regulatory) HR Anew

Clinical Research Coordinator I Adams Clinical

Inpatient Unit Clinical Research Coordinator I Adams Clinical

Research Associate 2 - College of Optometry, Vision Science Department University of Houston

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