NewPer Diem Family Medicine Physician Assistant or Nurse Practitioner (Casual Employee) One MedicalPer Diem Family Medicine Physician Assistant or Nurse Practitioner (Casual Employee)DALLAS, TXOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.
Clinical 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.
Clinical Research Assistant / Dallas (Refraction exp. req.) Texas Retina AssociatesClinical Research Assistant / Dallas (Refraction exp. req.)Dallas, TX
Research 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.
Clinical Research Assistant Velocity Clinical Research IncClinical Research AssistantDallas, TXSummary: 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. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
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.
Clinical Research Associate (CRA) Dallas Medpace Holdings IncClinical Research Associate (CRA) DallasIrving, 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; 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 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; 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; 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; and Must be detail-oriented and efficient in time management.
Research Technician, Early Phase Clinical Research - Dallas, TX FortreaResearch Technician, 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.
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.
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.
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.
PRN Outpatient Visit Research Nurse I, Early Phase Clinical Research - Dallas, TX FortreaPRN Outpatient Visit Research Nurse I, Early Phase Clinical Research - Dallas, TXDallas, TexasWe 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.
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.
Lab Technician/Research Assistant University of Texas at DallasLab Technician/Research AssistantDallas, TXTo 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. Following the probationary period, this role may be eligible for a partial hybrid work schedule (a combination of remote and in-office work), subject to business needs and manager approval.
PRN Outpatient Visit Research Nurse I, Early Phase Clinical Research - Dallas, TX Fortrea IncPRN Outpatient 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.
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.
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 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.
Clinical Research Coordinator Act for HealthClinical Research CoordinatorDallas, TexasParticipates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets . Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).
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.
Clinical Research RN II- Dallas Sammons Texas OncologyClinical Research RN II- Dallas SammonsDallas, 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.
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.
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.
Research Assistant UNIVERSITY OF NORTH TEXAS SYSTEMResearch AssistantDenton, TXThe 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.
Non-Student Research Assistant, Chemistry UNIVERSITY OF NORTH TEXAS SYSTEMNon-Student Research Assistant, ChemistryDenton, TXOur 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.
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 Coordinator II Baylor Scott & White HealthClinical Research Coordinator IIDallas, TXCert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Obtain research certification related to your work area within one year. Develops research study budgets for new clinical trials and assists in the completion of all applicable research billing compliance procedures.
Clinical Research Coord 2 Baylor Scott & White HealthClinical Research Coord 2Plano, TXCert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Obtain research certification related to your work area within one year. Develops research study budgets for new clinical trials and assists in the completion of all applicable research billing compliance procedures.
Non-Student Hourly Research Assistant UNIVERSITY OF NORTH TEXAS SYSTEMNon-Student Hourly Research AssistantDenton, TXOur 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.
Hourly Research Assistant UNIVERSITY OF NORTH TEXAS SYSTEMHourly Research AssistantDenton, TXThe Henard Laboratory (https://bdi.unt.edu/people/calvin-henard.html) in The BioDiscovery Institute and the Department of Biological Sciences at the University of North Texas is seeking to hire a highly motivated Research Assistant to join our team. These projects apply molecular and synthetic biology tools and techniques; thus, candidate familiarity with PCR, molecular cloning, site-directed mutagenesis, DNA transformation, and microbial physiology and biochemistry is desired.
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.
Assistant General Counsel - Clinical Research Cook Children's Health Care SystemAssistant General Counsel - Clinical ResearchFort Worth, TXThis position provides expert advice on regulatory and legal matters related to System-wide biomedical research, clinical trials, grants, institutional compliance and governance, including the Research and Grants Administration Office (RAO). Patients benefit from the integrated system because it allows Cook Children's to use all of its resources to treat a patient and allows for easy communication between the various companies by physicians with a focus on caring for children and adolescents.
Supervisor Clinical Research Baylor Scott & White HealthSupervisor Clinical ResearchDallas, TXThis role provides direct oversight of staff and study operations, actively contributes to study start-up, recruitment, and ongoing study execution, and supports budget development, and grant administration/submission activities. The role will ensure efficient coordination of clinical research activities across the Division of Rehabilitation, Division of Sports Therapy and Research, and Division of Trauma and Behavioral Health.
International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research InstituteInternational Medical Graduate (IMG) - Clinical Research CoordinatorDenton, TexasAdditional 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.
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 I Baylor Scott & White HealthClinical Research Coordinator IDallas, TXObtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations. Performs research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
Clinical 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.
Assistant Director of Research Operations University of Texas at DallasAssistant Director of Research OperationsDallas, TXTo 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. The Assistant Director will lead efforts to submit grants and contribute to the implementation of brain health interventions and programs, while supporting collaborative research efforts.
Clinical Research Engagement Lead (CREL) - Central Region (Dallas/Ft Worth, TX) Genentech IncClinical Research Engagement Lead (CREL) - Central Region (Dallas/Ft Worth, TX)Dallas, TX$108,800–$202,000 / yearRelationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).
Clinical 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.
Clinical Research Associate II ICON PlcClinical Research Associate IIDallas, TXAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Clinical Research Nurse Coordinator Actalent IncClinical Research Nurse CoordinatorFort Worth, TX$40–$45 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. We are seeking a dedicated Clinical Research Nurse Coordinator who will play a pivotal role in the coordination and management of clinical trials and research studies.
Registered Nurse Pediatric Clinical Research Act for HealthRegistered Nurse Pediatric Clinical ResearchDallas, TexasTwo (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred) . You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation.
Professor & Director - Charles and Jane Pak Center for Mineral Metabolism and Clinical Research University of Texas Southwestern Medical CenterProfessor & Director - Charles and Jane Pak Center for Mineral Metabolism and Clinical ResearchDallas, TXThe operational goals of the Center are three-fold: 1) to identify and implement new knowledge of mineral metabolism and its disorders, 2) to educate staff, students, physicians, and scientists to conduct research in and manage patients with diseases of mineral metabolism, and 3) to provide excellence in care for people with diseases of mineral metabolism. The Center exists to advance medical knowledge of the causes and treatments of diseases of mineral metabolism through discovery, to instruct and educate health care personnel and scientists in research and clinical practice, and to provide excellence in clinical care of patients with such diseases.
Clinical Research Associate ICON PlcClinical Research AssociateDallas, TXFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
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. 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.
Non-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.
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.
Part Time Market Comparable Research Assistant Partner Valuation Advisors LLCPart Time Market Comparable Research AssistantPlano, TXRemoteThis role is primarily focused on identifying, verifying, and analyzing market rent comparables for seniors housing properties using a combination of phone outreach and online research tools. Conduct market rent comparable research for seniors housing properties across the U.S. Perform outbound calls to property operators, managers, and other market participants to gather rental rate and operational data.