51 Results for

Research Jobs in Prosper, TX

Jobs

Dallas, Texas11 days ago

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.

Irving (Dallas), Texas30+ days ago

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

Irving (Dallas), Texas30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Dallas, Texas11 days ago

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

Denton, Texas29 days ago

The 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.

Irving (Dallas), Texas18 days ago

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

Irving (Dallas), Texas30+ days ago

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

Plano, TX30+ days ago

Prepares 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.

New!

Denton, Texas2 days ago

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

Denton, Texas12 days ago

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

New!

Denton, Texas4 days ago

The 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.

denton, TX30 days ago

Full-time

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

Denton, Texas30+ days ago

The Postdoctorate Research Associate role is primarily focused on the independent technical delivery of and leadership in the development of projects/activities related to powder processing and alloy development for AM within CAAAM (caaam.unt.edu), a State of Texas funded multimillion dollar initiative with a multidisciplinary focus on further advancing the science and technology of additive manufacturing (AM). The selected candidate is expected to have experience in areas such as: processing of metallic/alloy powders, AM of metals and/or other powderbased manufacturing technologies such as hot isostatic pressing or spark plasma sintering of alloys/composites, alloy development including a strong background in physical metallurgy.

Garland, TEXAS30+ days ago

Remote

You will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.

New!

Dallas, Texas4 days ago

Remote

$65,000–$75,000 Per Year

The position collaborates with principal investigators, analytical laboratories, data scientists, statisticians, and software teams across the PTFI ecosystem to coordinate research operations, manage complex data workflows, and translate multi-omics datasets into analysis-ready resources and scientific outputs. Acting as connective tissue across research teams and data systems, the role helps design studies, coordinate sample logistics, oversee multi-omics data readiness, and support the development of analytical tools and publications that advance discovery and real-world applications.

Denton, Texas30+ days ago

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. 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.

Denton, Texas30+ days ago

Familiarity with one or more material diagnostic techniques such as infrared imaging and spectroscopy, thermal imaging, Raman spectroscopy for metals and ceramics, plasma emission spectroscopy, non-destructive ultrasonic spectroscopy and testing of materials, transient laser spectroscopy as well as other diagnostic methods will be preferred. The candidate will assist in advancing necessary instrumentation for data collection and analysis, integrating process diagnostics with closed-loop process control of AM platforms, and work with fellow researchers to implement machine learning algorithms based on in-situ data collection and analysis.

New!

Denton, TX4 days ago

CAAAM'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.

New!

Denton, TX4 days ago

Plano, TX30+ days ago

Prepares documents like the clinical protocol, investigator's brochure, case report forms, informed consent documents, and parts of an IND application. + Works with team managers and others to define the strategic initiatives, scope, goals and timelines of the research program.

Plano, TEXAS30+ days ago

As a Work From Home Research Panel Member, you will help research teams gather authentic reactions from consumers in Plano and across the United States. Join scheduled virtual focus groups, interviews, or short opinion studies and participate professionally.

Denton, Texas22 days ago

$82,000–$102,000 Per Year

The RIC unit provides guidance and assistance to researchers in the following areas: Human Subjects and Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), Institutional Biosafety Committee (IBC), Conflict of interest (COI), Export controls, and Responsible conduct of research (RCR). Provides administrative oversight and support for the UNT Institutional Review Board Committee reviews of proposed human subjects research study protocols to ensure compliance with all federal government, funding agency regulatory guidelines, and university policies.

Denton, Texas30+ days ago

GCA aspires to be a model organization in the field of research administration, providing exceptional of externally funded sponsored projects and envision an environment that facilitates the University of North Texas' commitment to research and encourages continued efforts to attract additional research funding. Bachelor's degree in business administration, accounting, finance, auditing, public administration, or related field and five years of relevant administrative work or any equivalent combination of education, training, and experience.

Dallas, Texas11 days ago

The Clinical Support Associate assists the Clinical Operations Team within a limited scope of defined responsibilities in carrying out one of the assigned roles (collection/processing of laboratory samples, data entry of clinical data or administrative/front office support). Data Entry Responsibilities:Assist in the conduct of clinical trials by performing data entry tasks in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs under the direction of the Clinical Research Team.

Dallas, Texas30+ days ago

Remote

$90,000–$110,000 Per Year

This position collaborates with principal investigators, biostatisticians and key thought leaders to design studies that leverage American Heart Association unique assets, including its extensive registry site network, scientific expertise and data science capabilities. The American Heart Association’s 2028 Goal: Building on over 100 years of trusted leadership in cardiovascular and brain health, by 2028 the Association will drive breakthroughs and implement proven solutions in science, policy, and care for healthier people and communities.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Ophthalmology to join our Clinical Trial Management Group in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial Management Group in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers /Project Managers to join our Clinical Trial Management Group in Dallas,TX. 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.

Irving (Dallas), Texas30+ days ago

Responsibilities : Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Dallas, TX office.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus in Immunology, Rheumatology, Allergy, and/or Dermatology to join our Clinical Trial Management Group in our Dallas, TX office. 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.

Dallas, Texas30+ days ago

The Clinical Site Director oversees and manages all aspects of the clinical trial process including study feasibility, clinic staffing, patient recruitment, study conduct and regulatory compliance. 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.

Denton, Texas30+ days ago

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. As a student-focused, public research university, UNT prides itself on fostering a dynamic academic community that emphasizes excellence in education, cutting-edge research, and innovation.

Irving (Dallas), Texas30+ days ago

Responsibilities : Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Dallas office.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Immunology, Rheumatology, Allergy or Dermatology areas for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Responsibilities : Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm for a full-time, office-basedAssociate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position based in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to CNS/Neuroscience for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) based in our Dallas, TX office. 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.

Irving (Dallas), Texas30+ days ago

Responsibilities : Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research for a full-time, office-basedAssociate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

Dallas, Texas25 days ago

The PER Partner engages with the community, establishes and nurtures relationships with clinicians (internal and external), creates and manages participant referral patterns, expands site therapeutic and specialty capabilities, reviews patient health records, and ensures patient engagement for clinical trials. 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.

Dallas, Texas30+ days ago

Remote

$70,000–$90,000 Per Year

Develop and deliver site and program-wide targeted education and training materials, utilizing collected insights; this includes fully developing and implementing national educational webinars for clinicians and healthcare leadership, researching and creating patient and clinician educational materials, etc. Prospect new hospitals and associated clinics by working with established customers, routinely reviewing their data, consulting on identification of patients and clearly conveying the referral process to all involved site staff, Serve as main account manager of participating sites.

Carrollton, TX24 days ago

The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Internistto join our expanding team of clinical professionals.

Richardson, TX30+ days ago

The LVN will collaborate with the research team to ensure the successful implementation of clinical trials, maintaining strict adherence to study protocols while delivering compassionate and comprehensive patient care. Job Summary:The Licensed Vocational Nurse (LVN) at our inpatient clinical research site is responsible for providing high-quality nursing care to patients participating in clinical research studies.

Richardson, Texas30+ days ago

Texas Oncology is the largest community oncology provider in the country and has approximately 530 providers in 280+ sites across Texas, our founders pioneered community-based cancer care because they believed in making the best available cancer care accessible to all communities, allowing people to fight cancer at home with the critical support of family and friends nearby. TheUS Oncology Network is supported by McKesson Corporation focused on empowering a vibrant and sustainable community patient care delivery system to advance the science, technology, and quality of care.

Dallas, Texas17 days ago

Remote

$110,000–$120,000 Per Year

Through strong interpersonal and leadership skills and the SMA’s broad general knowledge of cardiovascular care and science, the SMA works with the science volunteers to produce the Association’s Scientific Statements, Clinical Practice Guidelines, online and face-to-face educational programs, responses to proposed advocacy and policy stances for the Association, and other activities that involve input from clinical and research experts. Provide consultation, guidance, and approval on science aspects to internal Association staff who develop and maintain public and professional programs, patient and lay publications, Association websites, press releases, corporate relations, and marketing materials with health and science implications and other public-facing activities.

Irving (Dallas), Texas30+ days ago

Responsibilities : Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc; Perform administrative duties in conformity with company policies and procedures; Coordinate and schedule meetings, provide meeting minutes; Maintain databases/project specific status reports; Support filing and quality control reviews of our internal regulatory filing system; Manage study supplies; 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.

New!

Irving, TX4 days ago

Physician 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.

Dallas, Texas19 days ago

Remote

$100,000–$115,000 Per Year

The Scientific Lead supports growth of the PTFI laboratory network by identifying and onboarding high-capacity laboratories, aligning training resources and analytical workflows, and guiding harmonized data generation and interpretation across the ecosystem to enable biomarker discovery, cross-study comparability, and translation of molecular food composition data into biological and clinical insights. The American Heart Association’s 2028 Goal: Building on over 100 years of trusted leadership in cardiovascular and brain health, by 2028 the Association will drive breakthroughs and implement proven solutions in science, policy, and care for healthier people and communities.

Garland, Texas22 days ago

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

New!

Irving, TX4 days ago

Current 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.

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Research Jobs in Prosper, TX

Clinical Research Assistant Velocity Clinical Research, Inc.

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

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

Senior Clinical Research Coordinator Velocity Clinical Research, Inc.

Postdoctoral Research Associate - The Skellam Lab University of North Texas System

Dallas Clinical Research Project Coordinator Medpace, Inc.

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

Supervisor Clinical Research Baylor Scott & White Health

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

Research Assistant University of North Texas System

Hourly Research Assistant University of North Texas System

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

Postdoctoral Research Associate University of North Texas System

Remote Market Research Assistant Earn Up to $50/Task Occupons Quebec

Project Manager, Research and Data Workflow American Heart Association

Postdoctoral Research Associate | Spectroscopy and Materials Synthesize University of North Texas System

Postdoctoral Research Associate - CAAAM University of North Texas System

Postdoctoral Research Associate University of North Texas

Postdoctoral Research Associate | Spectroscopy and Materials Synthesize University of North Texas

Research Project Coord 1 Baylor Scott & White Health

Work From Home Research Panel Member AFG

Director Research Compliance University of North Texas System

Senior Research Analyst University of North Texas System

Clinical Support Associate Velocity Clinical Research, Inc.

Grant Proposal Manager, Clinical American Heart Association

Clinical Trial Project Manager - Ophthalmology - Dallas Medpace, Inc.

Clinical Trial Project Manager - Neuroscience - Dallas Medpace, Inc.

Clinical Trial Project Manager - Dallas, TX Medpace, Inc.

Clinical Trial Project Manager - Infectious Diseases - Dallas Medpace, Inc.

Clinical Trial Project Manager - Immunology - Dallas Medpace, Inc.

Director, Clinical Site Velocity Clinical Research, Inc.

Clinical Assistant or Associate Professor - Mechanical Engineering/Mechanical Engineering Technology/Engineering Management University of North Texas System

Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX Medpace, Inc.

Associate Clinical Trial Manager - PhD - Immunology - Dallas Medpace, Inc.

Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience - Dallas Medpace, Inc.

Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX Medpace, Inc.

Patient Experience & Recruitment Partner Velocity Clinical Research, Inc.

Program Implementation Manager, Clinical Studies American Heart Association

Physician - Internist ECN Operating LLC

LVN - Unit Clinician -7p-7a (FT, PT or PRN) Pillar Clinical Research, LLC

Medical Billing AR Analyst Texas Oncology

Science & Medicine Advisor American Heart Association

Clinical Trial Intern - 2026/2027 Grads Medpace, Inc.

Advanced Practice Provider II- Trauma Parkland Health Hospital System

Scientific Lead, Multi-omics American Heart Association

Advanced Practice Provider Sr.- Garland Texas Oncology

Advanced Practice Provider II- Cardiology Parkland Health Hospital System

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