NewClinical Research Coordinator JouléClinical Research CoordinatorDallas, TX$26–$30 / hourOverview: Join a busy, onsite clinical research site in Dallas, TX as a Clinical Research Coordinator, supporting vaccine and other clinical trials by coordinating study visits, assisting with informed consent, maintaining source documentation, and ensuring compliance with GCP/SOPs. You’ll partner closely with the PI, research staff, and participants to support screening, data entry, safety reporting, and day-to-day study operations with a strong focus on quality and patient experience.
NewInpatient Unit Clinical Research Assistant Adams ClinicalInpatient Unit Clinical Research AssistantDallas, TexasWorking under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
Clinical Research Assistant Adams ClinicalClinical Research AssistantDallas, TX$19.23–$23.08 / hourWorking under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
Clinical Research Coordinator I Dallas Research InstituteClinical Research Coordinator IDallas, TexasComplete 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. Summary: The Clinical Research Coordinator I will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are followed.
Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TX Fortrea IncOutpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TXDallas, TXWe are currently seeking a OPV (Outpatient Visit) Research Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
PRN Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TX Fortrea IncPRN Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TXDallas, TXWe are currently seeking a OPV (Outpatient Visit) Research Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
Clinical Research Assistant Stryde ResearchClinical Research AssistantPlano, TXFull timeYou're Perfect If: You've worked in a clinic setting in US and know how healthcare actually operates, you can switch from scheduling patients to creating excel/ppt to answering sponsor emails-all before lunch, you're comfortable with medical terminlogy and talking to patients about their care, you thrive on variety and don't mind wearing multiple hats every single day, and you want to use your clinic experience to help bring new treatmens to patients. What You'll Actually Be Doing: Clinic administration, patient scheduling, documentation, coordinating between patients, providers, and research teams, handling everything from scheduling to data entry to site communications, troubleshooting daily operational challenges (because something always comes up), and supporting the team while keeping every detail organized.
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.
Research Technician (HR Title: Research Assistant) Southern Methodist UniversityResearch Technician (HR Title: Research Assistant)Dallas, TXAbout SMU SMUs more than 12,000 diverse high-achieving students come from all 50 states and 90 countries to take advantage of the Universitys small classes, hands-on research opportunities, leadership development, community service, international study, and innovative programs. 75092true75092false Submission for the position Research Technician HR Title: Research Assistant - Job Number: DED00000460 false 75092false true Research Technician HR Title: Research Assistant DED00000460 Hourly Range: 21.12/hr - 41,184/yr.
Research Technician (Nights), Early Phase Clinical Research - Dallas, TX Fortrea IncResearch Technician (Nights), Early Phase Clinical Research - Dallas, TXDallas, TXAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
NewClinical Research Enrollment Assistant Adams ClinicalClinical Research Enrollment AssistantDallas, TexasThis role focuses on the hands-on execution of essential administrative and clinical tasks—such as scheduling, preparing visit materials, supporting participant flow, maintaining source documentation, and completing timely data entry—to ensure efficient site operations and high-quality study conduct. The enrollment RA works closely with the enrollment coordinators to provide insights that inform clinical judgment on participant eligibility and study suitability and assists with screening activities and accurate documentation in compliance with ICH-GCP, study protocols, and regulatory requirements.
PRN Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TX FortreaPRN Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TXDallas, TexasWe are currently seeking a OPV (Outpatient Visit) Research Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
Outpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TX FortreaOutpatient Visit Research Technician, Early Phase Clinical Research - Dallas, TXDallas, TexasWe are currently seeking a OPV (Outpatient Visit) Research Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
Clinical Research Coordinator II Iterative Scopes IncClinical Research Coordinator IIMansfield, TXLead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
VP, Non-Interventional Research - Collections Research Iterative Scopes IncVP, Non-Interventional Research - Collections ResearchDallas, TXWork cross-functionally with site operations leaders and executive leadership to identify and onboard the right sites and networks network to stand up and support collections studies across different therapeutic areas and specialty networks. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Outpatient Visit Research Nurse I, Early Phase Clinical Research - Dallas, TX Fortrea IncOutpatient Visit Research Nurse I, Early Phase Clinical Research - Dallas, TXDallas, TXWe are currently seeking an Outpatient Visit (OPV) Research Nurse, to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
Clinical 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.
Clinical Research Coordinator / Ophthalmology exp. required Texas Retina AssociatesClinical Research Coordinator / Ophthalmology exp. requiredDallas, 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.
Research Assistant I University of Texas at DallasResearch Assistant IRichardson, TX$36,764–$38,000 / yearTo the extent this position requires the holder to research, work on, or have access to critical infrastructure as defined in Section 117.001(2) 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. 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.
Clinical Research Specialist IntraCareClinical Research SpecialistDallas, TexasApplicants who have worked 2+ years in a pulmonary office and are familiar with patient assessments, spirometry, or chronic respiratory disease management will find this an excellent opportunity to transition into clinical research. Maintain comprehensive and organized study documentation, such as case report forms, regulatory paperwork, and study logs.
Clinical Research Assistant II SGS SAClinical Research Assistant IIRichardson, TXTasks may include but are not limited to Electronic Self-Assessment Questionnaire (ESAQ) administrations, check-in process, informed consent signing, instrumentation assist, photography assist, etc. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Clinical Research Assistant II (Contract) - On Call - 6-8 weeks SGS SAClinical Research Assistant II (Contract) - On Call - 6-8 weeksRichardson, TXTasks may include but are not limited to Electronic Self-Assessment Questionnaire (ESAQ) administrations, check-in process, informed consent signing, instrumentation assist, photography assist, etc. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Clinical Research Technician (Night shift), Early Phase Clinical Research - Dallas, TX FortreaClinical Research Technician (Night shift), Early Phase Clinical Research - Dallas, TXDallas, TexasAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Manager Clinical Research Baylor Scott & White HealthManager Clinical ResearchDallas, TXWorks with investigators and industry to develop scientific protocols, concepts and tools to conduct clinical research effectively. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits.
NewOutpatient Visit Research Nurse I / Paramedic, Early Phase Clinical Research - Dallas, TX FortreaOutpatient Visit Research Nurse I / Paramedic, Early Phase Clinical Research - Dallas, TXDallas, TexasWe are currently seeking an Outpatient Visit (OPV) Research Nurse or a Paramedic, to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
Clinical 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.
Senior Clinical Research Coordinator Velocity Clinical Research, Inc.Senior Clinical Research CoordinatorDallas, TexasFull timeImplement 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.
NewProject Manager, Clinical Research - New Site Build Iterative Scopes IncProject Manager, Clinical Research - New Site BuildDallas, TX$80,000–$110,000 / yearThis role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Clinical Research Coordinator Revival Research InstituteClinical Research CoordinatorDenton, TexasAdditional Qualifications: Expert 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. We are seeking a full-time Clinical Research Coordinator with a minimum of 1 year of clinical experience, for our Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow.
Clinical Research Coordinator II - Nurse Iterative Scopes IncClinical Research Coordinator II - NurseSouthlake, TXBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Supv Clinical Research Baylor Scott & White HealthSupv Clinical ResearchPlano, TXPrepares initial project submissions, amendment notifications, SAE reports, continuing review reports, and other reports for the IRB. Establishes and maintains good relations with the public, patients, and staff; promotes the department''s research programs.
Clinical Research Regulatory Specialist Baylor Scott & White HealthClinical Research Regulatory SpecialistDallas, TXThis includes protocol revisions or amendments for new treatments, administrative changes, subject population changes, funding, recruitment, site changes, informed consent changes, or dual enrollment. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorDallas, TX$32–$36 / hourThis position focuses on research participant recruitment and consenting, delivering concierge-level service throughout the clinical trial journey, and coordinating biospecimen collection in collaboration with clinical research nursing, laboratory teams, and hospital departments. The Clinical Research Coordinator II (Non-RN) plays a key role in all aspects of clinical research, including screening and enrolling participants, coordinating their care and follow-up, and ensuring strict adherence to regulatory and protocol requirements.
Clinical Research Coordinator II Adams ClinicalClinical Research Coordinator IIDallas, TX$23–$28.37 / hourMaintain 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.
Clinical Research Coordinator II ObjectiveHealth IncClinical Research Coordinator IIDallas, TXNot 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. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
Project Manager, Clinical Research - New Site Build Iterative HealthProject Manager, Clinical Research - New Site BuildSouthlake, TX$80,000–$110,000 / yearThis role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Senior Clinical Research Coordinator Velocity Clinical Research IncSenior Clinical Research CoordinatorDallas, TXImplement 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 manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Required Licenses/Certifications: Phlebotomy if applicable and required by state lawIntravenous/Intramuscular dose administration and preparation if applicable and required by state lawCertified Clinical Research Coordinator through ACRP or SOCRA within six months of being in the role.
Project Manager, Clinical Research - New Site Build Iterative Scopes Inc.Project Manager, Clinical Research - New Site BuildDallas, TXThis role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials. As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from the ground up.
Clinical Research Coordinator II ObjectiveHealthClinical Research Coordinator IIDallas, TXNot 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. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
NewClinical Research Coordinator II - Nurse Iterative HealthClinical Research Coordinator II - NurseSouthlake, TXBy combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
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.
Clinical Research Coordinator ALS GlobalClinical Research CoordinatorIrving, TexasPerform routine facility and study-area opening and closing procedures, which may include unlocking and securing entrances, disarming and setting alarms, turning lights and equipment on or off, preparing materials for the next study day, and ensuring work areas are clean, stocked, and ready for use. Collaborate with investigators, project managers, clinical management, and other internal departments to communicate study progress, provide status updates, and support the preparation of protocols, interim reports, final reports, and sponsor deliverables.
Clinical Research Coordinator II - Nurse Iterative Scopes Inc.Clinical Research Coordinator II - NurseSouthlake, TXBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Clinical Research Scientist Revance Therapeutics IncClinical Research ScientistDallas, TXJob Summary: The Clinical Research Scientist develops, designs, and executes clinical and consumer research studies to assess the efficacy and consumer appeal of selected Revance products and technology. Collaborates closely with the Investigator and clinical staff in scheduling future appointments, explaining patient diairies, questionnaires, reporting of adverse events, recognizing serious adverse events.
Clinical Research Unit Manager Texas A&M AgriLife ResearchClinical Research Unit ManagerFort Worth, TXConducts various clinical procedures such as phlebotomy, finger sticks for Point of Care devices (ex- glucometer, hemoglobin, etc), vital sign assessment, anthropometrics, body composition analysis, collection of various biological samples (urine, stool, saliva, hair, blood, etc), and specialized assessments such as liver scanning, ultrasound, skin carotenoid assessment, etc. The Texas A&M AgriLife Institute for Advancing Health Through Agriculture, IHA, is the world's first academic institute to bring together precision nutrition, responsive agriculture, and social and behavioral research to reduce diet-related chronic disease and lower health care costs in a way that supports producers and the environment.
Clinical Research Unit Manager Texas A&MClinical Research Unit ManagerFort Worth, TexasConducts various clinical procedures such as phlebotomy, finger sticks for Point of Care devices (ex- glucometer, hemoglobin, etc), vital sign assessment, anthropometrics, body composition analysis, collection of various biological samples (urine, stool, saliva, hair, blood, etc), and specialized assessments such as liver scanning, ultrasound, skin carotenoid assessment, etc. The Texas A&M AgriLife Institute for Advancing Health Through Agriculture, IHA, is the world’s first academic institute to bring together precision nutrition, responsive agriculture, and social and behavioral research to reduce diet-related chronic disease and lower health care costs in a way that supports producers and the environment.
Research Coordinator 2 Methodist Health SystemResearch Coordinator 2Dallas, TXYour Job Requirements: • Bachelor degree or Medical Assistant in appropriate discipline • RN Degree preferred • Medical Assistant Certification, and/or a Certified Clinical Research Coordinator (CCRC) required • LVN or RN license, preferred • 2 or more years of related experience Your Job Responsibilities: • Available to sponsor monitors upon study site visits • Follow patients throughout study • Maintain statistical information • Following all rules and regulations from the FDA, IRB, and other agencies designated by the sponsors. Named one of the fastest-growing health systems in America by Modern Healthcare, Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others.
Senior Clinical Research Finance Specialist Iterative HealthSenior Clinical Research Finance SpecialistSouthlake, TX$85,000–$105,000 / yearYou will own core transactional AR workflows, including monitoring sponsor and site-level accounts, supporting timely collections, posting cash in RealTime CTMS, and assisting with invoicing as needed. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
PRN Telemetry Technician - Early Phase Clinical Research - Dallas, TX Fortrea IncPRN Telemetry Technician - Early Phase Clinical Research - Dallas, TXDallas, TXRepetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment. The important thing for us is you are comfortable working in an environment that is: Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Clinical Research Coordinator ALS LtdClinical Research CoordinatorIrving, TXPerform routine facility and study-area opening and closing procedures, which may include unlocking and securing entrances, disarming and setting alarms, turning lights and equipment on or off, preparing materials for the next study day, and ensuring work areas are clean, stocked, and ready for use. Prepare study areas, patch booths, test materials, volatilized and non-volatilized patches, dilutions, and other supplies required for study conduct, and complete all applicable preparation, equipment, booth, cart, and study logs.