68 Results for

3rd Shift Research Jobs in Texas

Jobs

Dallas, Texas14 days ago

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. 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.

Ft Worth, Texas29 days ago

Our founders pioneered community-based cancer care because they believed in making the best available cancer care accessible to all communities, allowing people to fight cancer at home with the critical support of family and friends nearby. Our mission is still the same today—at Texas Oncology, we use leading-edge technology and research to deliver high-quality, high-touch, evidence-based cancer care to help our patients achieve “More breakthroughs.

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.

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.

Lubbock, TX13 days ago

The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act is a federal statute requiring colleges and universities participating in federal financial aid programs to maintain and disclose campus crime statistics and security information. Trained in immunology and microbiology methods, including bacterial culturing, Gram staining, biochemical and ATP assays, antibiotic susceptibility testing, immunodiffusion, and blood cell analysis.

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.

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.

Dallas, TX18 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.

New!

Austin, TX2 days ago

The Graduate Research Assistant will support mixed-methods research on clinical reasoning and AI use in healthcare, analyzing multimodal data including chat transcripts, videos, surveys, and interviews. They will conduct quantitative and qualitative analyses, code data, interpret findings, and develop analytic memos while collaborating with faculty and research teams.

New!

San Antonio, Texas5 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.

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.

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.

Dallas, Texas14 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.

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.

Fort Worth, Texas26 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. The UNT System includes the University of North Texas in Denton and Frisco, the University of North Texas at Dallas and UNT Dallas College of Law, and University of North Texas Health Fort Worth.

Fort Worth, Texas25 days ago

Maintain accurate records, code and verify data in accordance with specified research protocol and coding procedures enter data into a computer database and/or spreadsheet application for subsequent analysis. Ranked among the top 50 medical schools for seven consecutive years, UNT Health is a 33-acre graduate school located in the city’s Cultural District with a local economic impact of $500 million annually.

Dallas/Fort Worth, TX30+ days ago

The Medical Assistant – Patient Recruiter plays a key role in identifying potential participants, conducting phone screenings, scheduling visits, supporting the consent process, and ensuring accurate documentation. Prime Clinical Research partners with pharmaceutical companies, biotechnology organizations, and contract research organizations to conduct clinical trials that advance medical innovation and improve patient outcomes.

Houston, TX11 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.

Dallas/Fort Worth, TX30+ 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.

New!

The Woodlands, Texas5 days ago

$50,000–$85,000

We are a growing private rheumatology practice in The Woodlands seeking an experienced Clinical Research Coordinator (CRC) to support and manage clinical trials focused on autoimmune and inflammatory conditions. Join a dedicated team committed to improving patient outcomes through high-quality clinical research in a collaborative and patient-centered setting.

San Antonio, TX19 days ago

Full-time

Use and maintain an autorefractor, phoropter, auto and manual keratometer, tonopen, Humphrey and Goldman visual field machines, corneal topographer, A-scan machine, pachymeter, specular microscope, ophthalmic photography equipment, slit lamp, potential acuity meter, brightness acuity test, color vision plates, stereo vision test, and personal computers. Our company has been operating for over 14 years and provides Information Technology engineering and support services, Healthcare IT, and clinical staffing to a variety of clients from the following industries: Federal Civilian and Defense Government Agencies (FLDOT, U.S. Air Force, U.S. Navy), Healthcare, Insurance, Manufacturing, Retail, and Real Estate.

New!

The Woodlands, Texas5 days ago

$60–$100

We 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.

Austin, Texas30+ days ago

Trains and supports health center staff on study participation according to PPGT Research SOPs and protocol including ensuring complete confidentiality of subjects and patients services, including proper and prompt transfers, purging and storage of records; schedule subject follow-up appointments within designated protocol timeframes; recruit, screen, consent and manage study subjects per protocol and GCP guidelines and PPGT Research SOPs; record and accurately reconcile subject stipends; dispense investigational product according to protocol and maintain accurate and timely product accountability. Integrated Approaches to Testing and Assessment (IATA) certification, Collaborative Institutional Training Initiative (CITI) Training, Good Clinical Practice (GCP), Human Subjects Protection (HSP), Responsible Conduct of Research (RCR) modules must be successfully completed.

Austin, Texas30+ days ago

Tyler, Texas29 days ago

El Paso, Texas30+ days ago

Dallas/Fort Worth, TX30+ days ago

This role works closely with the Principal Investigator and clinical research team to provide protocol-driven medical oversight, participant safety management, and high-quality clinical documentation. The NP Sub-Investigator plays an essential role in protecting participant safety while ensuring studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements.

Pearland, TX27 days ago

AIH Research partners with Community Health Network to bring FDA‑approved studies to patients who need them most—improving health equity while delivering high‑quality data to sponsors. Flexible schedule, Paid time off, Health insurance, Dental insurance, Vision insurance, Life insurance, Disability insurance, Referral program, Employee discount, Pet rider program, Mileage reimbursement, OtherJob Type.

Lubbock, TX20 days ago

$48,000–$63,700 Per Year

Department faculty recognitions and awards include membership in the US National Academy of Engineering and foreign Academies of Engineering and Science, recognitions as Thomson-Reuters highly cited scholars, receipts of NSF CAREER awards, PECASE awards, and Department of Defense Young Investigator awards. This group’s research directed by Fazle Hussain, PhD, NAE, has so far addressed the effects of cell signaling pathways on cancer cell mechanics, fluid mechanics, and metastasis, as well as the mitigating effects of naturopathic compounds, and nano therapy.

Austin, TX30+ days ago

Remote

RD Nutrition Consultants is seeking a Registered Dietitian Nutritionist (RDN) for a part-time, 100% remote Telehealth role supporting a long-term weight management clinical research study. RD Nutrition Consultants, LLC is a Registered Dietitian Nutritionist Consulting firm that provides Dietitians to health care facilities throughout the United States.

Dallas, TX30+ days ago

Join Clinitiative Health Research's ClinPI Program, a nationwide initiative that matches board-certified physicians with local, flexible clinical trial opportunities based on your specialty and availability. Are you a hospitalist, private practice physician, or existing principal investigator looking to supplement your income and contribute to medical innovation—without adding administrative burden or sacrificing your clinical autonomy?

New!

Houston, TX2 days ago

Qualifications include a PhD in a related field, with preferred experience in cardiovascular research, molecular techniques, mouse models, and cell culture. Skills required are strong analytical, communication, and presentation abilities, along with laboratory maintenance knowledge.

San Antonio, TX20 days ago

The Supervisor serves as the first-line operational lead for clinical research staff—driving execution, resolving day-to-day challenges, monitoring performance, and ensuring the successful delivery of clinical trials. · Provide day-to-day direction, workflow coordination, and functional oversight for Study Coordinators, Recruiters/Screeners, Data Coordinators, and Lab Support Staff, in partnership with their respective supervisors.

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, research team, Study Sponsor/CROs, potential subjects, and referral sources.

New!

Houston, TX1 day ago

The Postdoctoral Research Associate conducts specialized research in cardiovascular science, utilizing expertise in molecular cloning, mouse heart dissection, cardiomyocyte culture, and related techniques. Qualifications require a PhD in a related field, with preferred experience in cardiovascular disease research and laboratory techniques.

San Antonio, Texas13 days ago

Irving (Dallas), Texas21 days ago

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

JBSA-Lackland, TX30+ days ago

Use and maintain an autorefractor, phoropter, auto and manual keratometer, tonopen, Humphrey and Goldman visual field machines, corneal topographer, A-scan machine, pachymeter, specular microscope, ophthalmic photography equipment, slit lamp, potential acuity meter, brightness acuity test, color vision plates, stereo vision test, and personal computers. Refractive Research Technician Specific Duties: The duties include, but are not limited to the following; • Perform initial medical screening of patients including history, distance and near visual acuity with and without correction or pinhole, pupillary light reflex, and application tonometry; assist with all aspects of patient care.

Irving (Dallas), Texas30+ days ago

Responsibilities : Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB); Maintain timelines for study start-up through both internal and external collaboration; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and. Qualifications : Bachelor's degree required, preferably in a Life Sciences field; 1-5+ years of prior experience as a study coordinator or within the pharmaceutical industry, specializing in study start up is required; Excellent organization and communication skills; and.

Houston, TX30+ days ago

In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings. · Responsible for accurately maintaining and recording Investigational Product receipt from the Sponsor and its use.

Denton, Texas15 days ago

The candidate will assist in the lab of Dr. Mohammad Omary on research in the fields of Inorganic and Materials Chemistry, conducting research into metal-organic frameworks (MOFs) and their applications, utilizing Monte Carlo and crystal building simulations. Our faculty and graduate students successfully compete for research funds from both public and private sources, publish their groundbreaking research in top scientific journals, and are frequently highlighted and interviewed in the media.

New!

Denton, Texas5 days ago

Our faculty and graduate students successfully compete for research funds from both public and private sources (see below), publish their groundbreaking research in top scientific journals, and are frequently highlighted and interviewed in the media. We are growing with the North Texas region, employing more than 14,000 employees, educating a record 49,000+ students across our system, and awarding nearly 12,000 degrees each year.

Sugar Land, Texas30+ days ago

Accurately performs and documents visual acuity, confrontational visual fields, evaluation of motility, pupillary function tests, dilation, and ocular tonometry. has three certified research centers and is home to the Greater Houston Retina Research Center, one of the country’s leading sites for retinal research.

Sugar Land, Texas30+ days ago

Essential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.

Katy, Texas30+ days ago

denton, TX30+ days ago

Full-time

Additional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.

New!

San Antonio, TX1 day ago

The Research Assistant supports specialized educational/social science research projects under supervision, handling tasks like recruitment, data collection, and project operations. Responsibilities include conducting research as per plans, scheduling subjects, organizing data, reviewing literature, and performing other duties.

Fort Worth, Texas15 days ago

The Department of Population & Community Health in the College of Public Health at The University of North Texas Health Science Center at Fort Worth advances applied public health research, community engaged scholarship, and graduate education. Faculty, staff, and trainees work together to support evidence informed practice, community partnerships, and public health workforce development aligned with the School of Public Health’s strategic priorities.

New!

Dallas, TX3 days ago

Assists with regulatory duties as they relate to coordination of clinical trials, to include, but not limited to: Providing appropriate study training tools for study team members with appropriate documentation, maintenance and completion of Delegation of Authority Log, sponsor and vendor communication documents, IP/device documentation, etc. Performs study-related procedures that have been delegated by PI according to study protocol (i.e. vital signs, EKG, phlebotomy, pulmonary function testing, urine pregnancy and drug testing, processing blood, or any other procedures required per protocol or ordered by study investigator) and documents appropriately on source documents.

New!

Austin, TX2 days ago

This is a Research Assistant Internship available to current UT students, focusing on Project DUAL, which studies how bilingual experiences influence young adult development. The internship is unpaid, flexible (remote, hybrid, or on-site), with 6 hours per week, starting immediately, and continuing until December 31, 2026.

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3rd Shift Research Jobs in Texas

Clinical Research Assistant Velocity Clinical Research, Inc.

Oncology Clinical RN-Ft Worth, Tx Texas Oncology

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

Clinical Research Assistant (Round Rock) Austin Retina Associates

Medical Student Research Asst - Singh Texas Tech University

San Marcos-Clinical Research Assistant Austin Retina Associates

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

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

Graduate Research Assistant (Mixed-methods and Multimodal Clinical Reasoning Analysis) The University of Texas at Austin

Clinical Research Coordinator Pinnacle Clinical Research

Clinical Research Assistant Retina Consultants of Texas

Bilingual Clinical Research Assistant (Spanish) Retina Consultants of Texas

Senior Clinical Research Coordinator Velocity Clinical Research, Inc.

Clinical Research Coordinator Assistant (CRCA) Flourish Research

Research Assistant II (Rater) University of North Texas System

Research Assistant II University of North Texas System

Medical Assistant – Clinical Research Patient Recruiter HR Anew

Clinical Research Nurse II AES Integrated Resources, Inc

Clinical Research Coordinator (without Regulatory) HR Anew

Clinical Research Coordinator Advanced Rheumatology of Houston

Refractive Research Technician OnesourcePCS, LLC

Clinical Research Chart QA/Auditor Advanced Rheumatology of Houston

Clinical Research Coordinator Planned Parenthood of Greater Texas

Clinical Research RN Texas Oncology

Clinical Research Nurse Sr.- Tyler Texas Oncology

Clinical Research RN Sr-Grandview, El Paso, Tx Texas Oncology

Nurse Practitioner (NP) – Clinical Research Sub-Investigator HR Anew

Clinical Research Regulatory Coordinator Advances in Healthcare

TTU Post Doctoral Research Associate Texas Tech University

Registered Dietitian - 100% Remote Clinical Research Role RD Nutrition Consultants

Clinical Research Principal Investigator (MD or DO Only -All Specialties Welcome Clinitiative Health Research

Postdoctoral Research Associate Texas A&M University

Clinical Research Supervisor Urology San Antonio

Clinical Research Coordinator I Flourish Research

Postdoctoral Research Associate Texas A&M

Research RN Sr-San Antonio, Tx Texas Oncology

Dallas Clinical Research Project Coordinator Medpace, Inc.

Ophthalmology Tech - Refractive Research ERP International

Study Start-Up Coordinator – Clinical Research Coordinator Experience Medpace, Inc.

Clinical Research Coordinator aQua Dialysis

Research Assistant University of North Texas System

Non-Student Research Assistant, Chemistry University of North Texas System

Clinical Research Technician Retina Consultants of Texas

Clinical Research Physician - Metabolic or Hepatology - part time (16 hours per week) Alcanza Clinical Research

Clinical Research Principal Investigator - Neurologist Alcanza Clinical Research

International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLC

Research Area Specialist-Associate UT Health San Antonio

Postdoctoral Research Associate University of North Texas System

Clinical Research Coordinator - Unblinded - Contract Wake Research

Research Assistant Internship (Open to Current UT Students Only) The University of Texas at Austin Students

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