Parkland Health and Hospital SystemNewAdvanced Practice Provider II- Emergency General Surgery Parkland Health and Hospital SystemAdvanced Practice Provider II- Emergency General SurgeryFort Worth, TXCurrent licensure from the Texas Board of Nursing as an Advanced Practice Registered Nurse (APRN) with authorization to practice as a Family, Adult, Gerontology, Adult-Gerontology, Adult-Gerontology Acute Care, Acute Care, Pediatric, Pediatric Acute Care, Psychiatric Mental Health, or Women's Health Nurse Practitioner. Bachelor's Degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.
Parkland Health and Hospital SystemNewAdvanced Practice Provider II- Burns Parkland Health and Hospital SystemAdvanced Practice Provider II- BurnsArlington, TXCurrent licensure from the Texas Board of Nursing as an Advanced Practice Registered Nurse (APRN) with authorization to practice as an Adult-Gerontology Acute Care or Acute Care Nurse Practitioner and a Pediatric Acute Care Nurse Practitioner. Bachelor's degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.
Parkland Health and Hospital SystemNewAdvanced Practice Provider II- Trauma Parkland Health and Hospital SystemAdvanced Practice Provider II- TraumaDallas, TXPhysician Assistant: Bachelor's Degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors. Performs all clinical practitioner service activities in the designated specialty area, including obtaining histories, performing physical exams, making assessments, and ordering tests to adequately assess, determine diagnoses, and plan care.
Parkland Health and Hospital SystemNewAdvanced Practice Provider II- Adult Parkland Health and Hospital SystemAdvanced Practice Provider II- AdultGrand Prairie, TXCurrent licensure from the Texas Board of Nursing as an Advanced Practice Registered Nurse (APRN) with authorization to practice as a Family, Adult, Gerontology, Adult-Gerontology, Adult-Gerontology Acute Care, Acute Care, Pediatric, Pediatric Acute Care, Psychiatric Mental Health, or Women's Health Nurse Practitioner. Bachelor's Degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.
Parkland Health and Hospital SystemNewAdvanced Practice Provider II- Cardiology Parkland Health and Hospital SystemAdvanced Practice Provider II- CardiologyGrand Prairie, TXCurrent licensure from the Texas Board of Nursing as an Advanced Practice Registered Nurse (APRN) with authorization to practice as a Family, Adult, Gerontology, Adult-Gerontology, Adult-Gerontology Acute Care, Acute Care, Pediatric, Pediatric Acute Care, Psychiatric Mental Health, or Women's Health Nurse Practitioner. Bachelor's Degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.
Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate)Irving, TXRemoteConduct 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.
Medpace, Inc.Clinical Research Associate (CRA) - Dallas Medpace, Inc.Clinical Research Associate (CRA) - DallasIrving (Dallas), TexasResponsibilities : 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.
Medpace Holdings IncClinical Research Associate PhD in Life Sciences Medpace Holdings IncClinical Research Associate PhD in Life SciencesIrving, TXConduct 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.
Texas Retina AssociatesClinical Research Coordinator / Ophthalmic exp. required - Dallas Texas Retina AssociatesClinical Research Coordinator / Ophthalmic exp. required - DallasDallas, TXTexas 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.
PRIME CLINICAL RESEARCH INCClinical Research Coordinator PRIME CLINICAL RESEARCH INCClinical Research CoordinatorMansfield, TXPRIME 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.
UNIVERSITY OF NORTH TEXAS SYSTEMResearch Assistant II (Outreach) UNIVERSITY OF NORTH TEXAS SYSTEMResearch Assistant II (Outreach)Fort Worth, TXTitle: 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.
Medpace, Inc.Clinical Research Associate - PhD in Life Sciences Medpace, Inc.Clinical Research Associate - PhD in Life SciencesIrving (Dallas), TexasResponsibilities : 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.
Velocity Clinical Research, Inc.Senior Clinical Research Coordinator Velocity Clinical Research, Inc.Senior Clinical Research CoordinatorDallas, TexasImplement 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.
University of North Texas SystemResearch Assistant II (Outreach) University of North Texas SystemResearch Assistant II (Outreach)Fort Worth, TexasThe 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.
HR AnewClinical Research Coordinator (without Regulatory) HR AnewClinical Research Coordinator (without Regulatory)Mansfield, TX$45,000–$55,000 / yearPrime 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.
MRINetwork JobsClinical Research Coordinator MRINetwork JobsClinical Research CoordinatorDallas, TexasClinicalResearch #CRCJobs #ClinicalTrials #HealthcareCareers #DallasJobs #ResearchCoordinator #NowHiring #MedicalResearch #OnsiteJob #TexasCareers. The position involves coordinating study activities, collecting data, ensuring compliance, and collaborating with physicians, sponsors, and research teams to keep studies on track and accurate.
Texas OncologyNewOncology Clinical Research RN Sr.- Flower Mound Texas OncologyOncology Clinical Research RN Sr.- Flower MoundFlower Mound, TexasOur 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.
Adams ClinicalClinical Research Coordinator I Adams ClinicalClinical Research Coordinator IDeSoto, TX$45,760–$56,160 / yearSupport 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.
Adams ClinicalInpatient Unit Clinical Research Coordinator I Adams ClinicalInpatient Unit Clinical Research Coordinator IDeSoto, TX$45,760–$56,160 / yearSupport 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.
Adams ClinicalClinical Research Administrative Coordinator Adams ClinicalClinical Research Administrative CoordinatorDeSoto, TX$37,440–$45,760 / yearAs a liaison between clinicians and research coordinators, participants, and healthcare providers, a successful applicant will work directly with treatment seeking populations scheduling, educating, and assisting participants to foster seamless flow of office visits and operations. Place calls, texts, and emails to potential study participants who missed or rescheduled their appointment to help them arrange a new appointment time and maintain their visit progress in coordination with office staff.
Adams ClinicalClinical Research Recruitment Coordinator Adams ClinicalClinical Research Recruitment CoordinatorDeSoto, TX$18–$22 / hourAs a member of our outreach team, the successful applicant will work directly with treatment seeking populations identifying, educating, and recruiting participants in our clinical trials. 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.
Adams ClinicalInpatient Unit Clinical Research Coordinator II Adams ClinicalInpatient Unit Clinical Research Coordinator IIDeSoto, TX$42,000–$66,650 / yearMaintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs. This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.
Medpace Holdings IncDallas Clinical Research Project Coordinator Medpace Holdings IncDallas Clinical Research Project CoordinatorIrving, TXEngage 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; • Coordinate project meetings and produce quality meeting minutes. 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.
Clinitiative Health ResearchClinical Research Principal Investigator (MD or DO Only -All Specialties Welcome Clinitiative Health ResearchClinical Research Principal Investigator (MD or DO Only -All Specialties WelcomeDallas, TXJoin 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?
University of North Texas SystemResearch Assistant III University of North Texas SystemResearch Assistant IIIFort Worth, TexasThe research assistant will help coordinate scheduling the subjects’ visits to the lab and communicate with the faculty at the Department of Internal Medicine, setup the lab for testing and assist the PI for neurovascular assessments, conduct the IHT/sham intervention train for the study participants/subjects. Employees in this job may be responsible for conducting research on, working on, or having the ability to access critical organizational infrastructure and they must be able to maintain the security and integrity of the infrastructure related to this role.
Medpace Holdings IncStudy Start Up Coordinator - Clinical Research Coordinator Experience Medpace Holdings IncStudy Start Up Coordinator - Clinical Research Coordinator ExperienceIrving, TXCommunicate with research sites (doctors 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 Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges. 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, eco-friendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace.
Adams ClinicalSenior Clinical Research Laboratory Technician Adams ClinicalSenior Clinical Research Laboratory TechnicianDeSoto, TX$50,000–$60,000 / yearThe Senior Laboratory Technician provides operational leadership for laboratory activities supporting ongoing clinical trials while overseeing and guiding Laboratory Technicians to ensure efficient, compliant, and high-quality lab operations. This role manages daily laboratory workflows and oversees specimen collection, processing, documentation, and shipment in accordance with study protocols, ICH-GCP guidelines and site SOPs.
UNIVERSITY OF NORTH TEXAS SYSTEMResearch Assistant UNIVERSITY OF NORTH TEXAS SYSTEMResearch Assistantdenton, TXJob Duties: This person will primarily work with the graduate students on the project to train them and aid with their organic and inorganic synthesis of the hydrophobic porous and non-porous materials; s/he also will work closely with the PI, to track the execution of tasks with weekly project meetings from both the technical and management sides. 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 the University of North Texas Health Science Center at Fort Worth.
University of North Texas SystemResearch Assistant University of North Texas SystemResearch AssistantFort Worth, TexasRanked 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. Employees in this job may be responsible for conducting research on, working on, or having the ability to access critical organizational infrastructure and they must be able to maintain the security and integrity of the infrastructure related to this role.
HR AnewNurse Practitioner (NP) – Clinical Research Sub-Investigator HR AnewNurse Practitioner (NP) – Clinical Research Sub-InvestigatorMansfield, TXThis 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.
IQVIA Holdings IncResearch Scheduler IQVIA Holdings IncResearch SchedulerIrving, TX$25,900–$64,800 / yearnEssential Duties and Responsibilities\n \nEssential and other important responsibilities and duties may include but are not limited to the following:\n\n Daily confirmation of all on-site clinic and off-site appointments.\n \n\n Receive, screen and coordinate telephone calls from healthcare providers.\n \n\n Assist with maintaining and updating all provider addresses and phone numbers\n \n\n Receive incoming correspondence and review/forward to appropriate staff.\n \n\n Perform a variety of administrative duties including but not limited to answering phones; faxing and filing of confidential documents; and basic Internet and email utilization.\n \n\n Provide excellent customer service to all internal and external customers.\n Our IDS team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.\n \nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Baylor Scott & White HealthClinical Research Coord 1 Baylor Scott & White HealthClinical Research Coord 1Plano, TXPerforms research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met. Examples include providing in-service education for healthcare professionals and working with Pharmacy to ensure smooth project flow.
University of North Texas SystemPostdoctoral Research Associate - The Skellam Lab University of North Texas SystemPostdoctoral Research Associate - The Skellam LabDenton, TexasThe Departments of Chemistry and Biological Sciences, and the BioDiscovery Institute, at the University of North Texas are equipped with modern facilities for all aspects of the research and have a strong community of research groups in biochemistry and molecular biology for a stimulating intellectual environment. This position will investigate the use of P450s as biocatalysts in Nicotinana benthamiana and / or filamentous fungi, testing approaches for enhancing interactions with redox partners, ensure correct anchoring, and designing mutagenesis experiments to diversify substrate scope.
UNIVERSITY OF NORTH TEXAS SYSTEMNewPostdoctoral Research Associate - Materials Science and Engineering UNIVERSITY OF NORTH TEXAS SYSTEMPostdoctoral Research Associate - Materials Science and EngineeringDenton, TXD. degree in Metallurgical or Materials Science and Engineering or related field, at least two to five years of research experience and significant number of refereed scientific articles in high-quality journals demonstrating a strong background in physical metallurgy, phase transformations, titanium alloys, materials characterization (especially scanning and transmission electron microscopy, focused ion beam microscopy, and atom probe tomography), thermodynamics and computational modeling skills. The Department of Materials Science and Engineering provides a high quality education to our student population through excellence and innovation in teaching and research in order to serve the scientific and engineering needs of the state of Texas and the nation.
Medpace, Inc.Dallas Clinical Research Project Coordinator Medpace, Inc.Dallas Clinical Research Project CoordinatorIrving (Dallas), TexasResponsibilities : 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.
Texas A&M AgriLife ResearchPostdoctoral Research Associate Texas A&M AgriLife ResearchPostdoctoral Research AssociateDallas, TXWhen you choose to work for Texas A&M AgriLife, you become part of an organization that is an established leader in agriculture and life sciences with a wide range of capabilities to meet the needs of our statewide, national, and international constituents. Texas A&M AgriLife Research - Dallas Center (https://dallas.tamu.edu/) is seeking a highly motivated individual to join the Controlled Environment Agriculture (CEA) Engineering Lab as a Postdoctoral Research Associate.
University of North Texas SystemPostdoctoral Research Associate University of North Texas SystemPostdoctoral Research AssociateFort Worth, TexasThe Center also supports numerous K-12 science outreach programs, offering summer science camps, campus tours, and in-school events that introduce students to anatomy and its relationship to medical education. The Center is also home to the Structural Anatomy and Rehabilitation Sciences (STARS) PhD program that prepares graduate students to join the workforce as researchers and anatomy educators.
Medpace, Inc.Study Start-Up Coordinator – Clinical Research Coordinator Experience Medpace, Inc.Study Start-Up Coordinator – Clinical Research Coordinator ExperienceIrving (Dallas), TexasResponsibilities : 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.
Children's Medical CenterNewClinical Research Nurse Children's Medical CenterClinical Research NurseDallas, TXSummary: The Clinical Research Nurse performs an essential role supporting the principal investigator in the conduct of clinical trials to ensure compliance with all aspects of the protocol and accuracy of data collection. We are committed to delivering culturally effective care, creating meaningful partnerships in the communities we serve, and equipping and developing our team members to make Children's Health a place where everyone can contribute.
UNIVERSITY OF NORTH TEXAS SYSTEMPostdoctoral Research Associate UNIVERSITY OF NORTH TEXAS SYSTEMPostdoctoral Research Associatedenton, TXCAAAM's Institute for Transformative Education in Additive Manufacturing-or ITEAM-provides courses, seminars, workshops, symposia, in-lab training sessions, and summer camps for industry and community colleges. 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 the University of North Texas Health Science Center at Fort Worth.
University of Texas Southwestern Medical CenterOpen Rank Positions of Epidemiology in Brain Health Research University of Texas Southwestern Medical CenterOpen Rank Positions of Epidemiology in Brain Health Researchdallas, TXThe institute fosters multidisciplinary research and is committed to building partnerships among basic, clinical, and population scientists to achieve its mission: delivering the best possible patient care today while creating a future of better treatment and prevention through discovery and innovation. Additionally, the Dallas-Fort Worth metroplex, home to 7.8 million people, features a large and diverse population\u201441 percent Hispanic and 24 percent African American\u2014offering exceptional opportunities for population health research.
University of Texas at ArlingtonPost Doctoral Research Associates University of Texas at ArlingtonPost Doctoral Research AssociatesArlington, TXThe University of Texas at Arlington (UTA) is located in the heart of the Dallas-Fort Worth-Arlington metroplex, a vibrant and diverse metropolitan area that is home to over 7 million people, one of the fastest-growing tech economies in the United States, and a wide array of arts, entertainment, and cultural activities. The successful candidate will work at the interface of computational genomics, AI-driven modeling, and translational oncology, analyzing large-scale multi-omic datasets from pediatric cancer cohorts.
University of North Texas SystemNon-Student Research Assistant, Chemistry University of North Texas SystemNon-Student Research Assistant, ChemistryDenton, TexasOur 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.
University of North Texas SystemNewAssociate Director of AI/ML Research & Training University of North Texas SystemAssociate Director of AI/ML Research & TrainingFort Worth, Texas$92,940–$111,528 / yearThe role supports interdisciplinary research, develops training programs, and contributes to extramural funding efforts to enhance institutional research capacity and impact. 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.
University of Texas Southwestern Medical CenterTenure Track Faculty in Research University of Texas Southwestern Medical CenterTenure Track Faculty in Researchdallas, TXPreference will be given for expertise in neuroscience, immunology, molecular biology, stem cell biology, or cancer biology using state\u2010of\u2010the art technologies with a focus on mechanisms of human disease at a cellular or molecular level. The University of Texas Southwestern Medical Center, Department of Pathology is looking for exceptional individuals (MD, DO, MD/PhD DO/PhD or PhD) to develop or continue groundbreaking basic or translational science as independent investigators.
University of North Texas SystemNewNon-Student Hourly Research Assistant University of North Texas SystemNon-Student Hourly Research AssistantDenton, TexasOur 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. 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.
Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research Coordinatordenton, TXFull timeAdditional 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.
University of North Texas SystemNon-Student Research Assistant University of North Texas SystemNon-Student Research AssistantDenton, TexasResponsibilities will include maintaining mammalian cell cultures, performing immunology-based experiments, developing and optimizing cell-based assays, analyzing data, training students and junior personnel, maintaining accurate laboratory records, and contributing to manuscript, grant, and report preparation. 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.
UNIVERSITY OF NORTH TEXAS SYSTEMPostdoctoral Research Associate | Spectroscopy and Materials Synthesize UNIVERSITY OF NORTH TEXAS SYSTEMPostdoctoral Research Associate | Spectroscopy and Materials SynthesizeDenton, TXTitle: Postdoctoral Research Associate | Spectroscopy and Materials Synthesize Employee Classification: Postdoctoral Research Assoc Campus: University of North Texas Division: UNT-Provost SubDivision-Department: UNT-College of Science Department: UNT-Physics-122300 Job Location: Denton Salary: Salary will be commensurate with experience. plan, develop, and assemble advanced spectrometers; synthesize and characterize novel materials; initiate and conduct research; gather, analyze, and interpret data; connect with contemporary research activities/publications; document research activity, develop synthesize protocols.
IQVIA Holdings IncResearch Coordinator IQVIA Holdings IncResearch CoordinatorIrving, TX$43,400–$108,200 / yearManagement of Clinical Trial Patients • Collaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol • Educates the patient and family regarding protocol participation • Provides patient education regarding required study procedures • If the Research Coordinator is a Registered Nurse, educates the patient and family regarding clinical condition, and/or disease process • If the Research Coordinator is not a RN, he/she will schedule educational time with a RN • Identifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety • If the Research Coordinator is not an RN, he/she will schedule educational time with a RN • Coordinates, schedules, and ensures timely completion of protocol-required events and other requirements (e.g., pharmacokinetics or -dynamics, scans, study visits, QOL) • Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary • Evaluates patient's adherence to and documentation of self-administered protocol agents and the return of such agents • Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers • Evaluates patient's adherence to and documentation of self-administered protocol agents and return of such agents • Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers • Ensures appropriate communication between research and clinical staff related to patient-specific care needs • Ensures evidence-based symptom management as permitted by the protocol. • Informed Consent • Identifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception) • Describes and abides by institutional policy and processes for informed consent • Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient • Collaborates with the physician investigator to ensure initial and ongoing consent process is performed and documented • Assesses ongoing consent through discussions with patients and reinforcement of education • Assesses patient's understanding of the information provided during the informed consent process • Ensures timely re-consenting as needed by the physician investigator • Demonstrates understanding of tiered consent process when optional correlative studies (e.g., biospecimen, quality of life, patient-reported outcomes collections) are involved • Confirms informed consent is obtained prior to performing any study specific tasks.