50 Results for

Research Jobs in Melissa, TX

Jobs

New!

Plano, TX5 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.

New!

Plano, TX5 days ago

Current licensure from the Texas Board of Nursing as an Advanced Practice Registered Nurse (APRN) with authorization to practice as an Adult-Gerontology Acute Care or Acute Care Nurse Practitioner and a Pediatric Acute Care Nurse Practitioner. Bachelor's degree from an accredited college or university and successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.

New!

Plano, TX5 days ago

New!

Plano, TX5 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.

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, TX30+ days ago

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 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.

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, Texas25 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.

New!

Flower Mound, Texas2 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.

Richardson, TX30+ days ago

Other Qualifications To the extent this position requires the holder to research work on or have access to critical infrastructure as defined in Section 117.0012 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. Special Instructions Summary Important Message 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.

Irving, TX30+ days ago

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; • Coordinate project meetings and produce quality meeting minutes. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace.

Irving, TX30+ days ago

Communicate with research sites (doctors offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB)); Maintain timelines for study start-up through both internal and external collaboration; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, eco-friendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace.

Plano, TX14 days ago

Performs 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.

Irving (Dallas), Texas30+ 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.

Irving, TX30+ days ago

$25,900–$64,800 Per Year

nEssential Duties and Responsibilities\n \nEssential and other important responsibilities and duties may include but are not limited to the following:\n\n Daily confirmation of all on-site clinic and off-site appointments.\n \n\n Receive, screen and coordinate telephone calls from healthcare providers.\n \n\n Assist with maintaining and updating all provider addresses and phone numbers\n \n\n Receive incoming correspondence and review/forward to appropriate staff.\n \n\n Perform a variety of administrative duties including but not limited to answering phones; faxing and filing of confidential documents; and basic Internet and email utilization.\n \n\n Provide excellent customer service to all internal and external customers.\n Our IDS team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.\n \nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Carrollton, 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.

Irving, TX30+ days ago

$148,000–$175,500 Per Year

Support BTI and Sales: Provide sales support serving as voice of the market to help Insights teams create content and to drive engagement with clients to make progress against their critical priorities to grow their business. Develop new insights and ideas through thought leadership and offer compelling, actionable approaches to clients needs and requests that accelerate the clients ability to act.

Dallas, Texas18 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.

Plano, TX22 days ago

Your work will directly impact the design, architecture, and functionality of our offerings, collaborating with cross-functional teams to contribute to discussions on design and research, and leading the decision on which methods best suit key design questions. Chase is a leading financial services firm, helping nearly half of Americas households and small businesses achieve their financial goals through a broad range of financial products.

Irving, TX30+ days ago

$43,400–$108,200 Per Year

Management of Clinical Trial Patients • Collaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol • Educates the patient and family regarding protocol participation • Provides patient education regarding required study procedures • If the Research Coordinator is a Registered Nurse, educates the patient and family regarding clinical condition, and/or disease process • If the Research Coordinator is not a RN, he/she will schedule educational time with a RN • Identifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety • If the Research Coordinator is not an RN, he/she will schedule educational time with a RN • Coordinates, schedules, and ensures timely completion of protocol-required events and other requirements (e.g., pharmacokinetics or -dynamics, scans, study visits, QOL) • Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary • Evaluates patient's adherence to and documentation of self-administered protocol agents and the return of such agents • Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers • Evaluates patient's adherence to and documentation of self-administered protocol agents and return of such agents • Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers • Ensures appropriate communication between research and clinical staff related to patient-specific care needs • Ensures evidence-based symptom management as permitted by the protocol. • Informed Consent • Identifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception) • Describes and abides by institutional policy and processes for informed consent • Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient • Collaborates with the physician investigator to ensure initial and ongoing consent process is performed and documented • Assesses ongoing consent through discussions with patients and reinforcement of education • Assesses patient's understanding of the information provided during the informed consent process • Ensures timely re-consenting as needed by the physician investigator • Demonstrates understanding of tiered consent process when optional correlative studies (e.g., biospecimen, quality of life, patient-reported outcomes collections) are involved • Confirms informed consent is obtained prior to performing any study specific tasks.

Frisco, TX30+ days ago

Industry Competitive Benefits: We offer comprehensive benefit plans to include flexible vacation, two company-wide Mental Health Days off, access to the Headspace app, retirement savings, tuition reimbursement, employee incentive programs, and resources for mental, physical, and financial wellbeing. • Hybrid Work Model: Weve adopted a flexible hybrid working environment (2-3 days a week in the office depending on the role) for our office-based roles while delivering a seamless experience that is digitally and physically connected.

New!

Richardson, TX3 days ago

Performs some highly technical laboratory procedures, including animal handling, retrograde tracing procedures, perfusions, and immunohistochemistry; participates in regular meetings with other Center researchers and creates and maintains constructive collaborations with outside researchers. To 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.

New!

Richardson, TX3 days ago

$61,500–$136,100 Per Year

Blue Cross and Blue Shield of Illinois, Blue Cross and Blue Shield of Montana, Blue Cross and Blue Shield of New Mexico, Blue Cross and Blue Shield of Oklahoma, and Blue Cross and Blue Shield of Texas, Divisions of Health Care Service Corporation, a Mutual Legal Reserve Company, and Independent Licensee of the Blue Cross and Blue Shield Association. Knowledge of key software packages (word processing, data management, spreadsheet, statistical analysis and presentation) and experience with corporate programming languages (SAS, SPSS, among others).

Plano, Texas8 days ago

The CSM collaborates closely with cross‑functional partners including Regulatory Affairs, Quality, Medical Affairs, and Product Development to generate high‑quality clinical evidence that supports product safety, performance, and regulatory objectives. Position Overview: The Clinical Study Manager (CSM) is responsible for the planning, execution, and oversight of clinical investigations for medical devices across the product lifecycle, including pre‑market and post‑market studies.

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.

Irving, TX30+ days ago

Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, eco-friendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace. 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.

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.

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

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 /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

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.

New!

Plano, TX1 day ago

Texas Retina Associates is Texas’ largest, most experienced ophthalmology practice focused specifically on the diagnosis, medical and surgical management of diseases of the retina and vitreous. The position will report directly to the Clinical Operations Manager and will help the physician in the testing, examination, education, and treatment of patients.

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.

Dallas, TX30+ 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.

Richardson, Texas10 days ago

Remote

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.

Irving, TX30+ days ago

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 • Coordinate project meetings and produce quality minutes. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Free on-site parking Outdoor seating and workspace.

Irving, TX30+ days ago

Dallas Perks Dallas Campus Overview 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 America''s 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 What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. 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 Coordinate project meetings and produce quality minutes.

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.

Frisco, TX30+ days ago

Part-time

Guided by our mission of fulfilling dreams by building families, Pinnacle offers compassionate care, innovative technology, and comprehensive fertility treatment services to provide patients with a seamless and personalized journey to parenthood. Pinnacle Fertility is a leader in physician-centric fertility care, supporting high-performing fertility clinics and comprehensive service providers nationwide.

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.

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

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.

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.

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.

New!

Lewisville, TX6 days ago

Preferred Work Experience:Previous experience, typically obtained through PhD or postdoctoral work, in laboratory based molecular oncology research such that the participant will be familiar with the molecular genetic DNA tools used in oncology such as next-generation sequencing, tumor sequencing for therapy selection, and circulating tumor DNA analysis. Stay updated on developments in clinical Heme/ONC including new applications, clinical trial data, presentations and publications on the clinical utility of molecular testing, emerging biomarkers that affect the use of current testing and the development of new test modalities.

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Research Jobs in Melissa, TX

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Advanced Practice Provider II- Trauma Parkland Health and Hospital System

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

Clinical Research Associate PhD in Life Sciences Medpace Holdings Inc

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

Senior Clinical Research Coordinator Velocity Clinical Research, Inc.

Oncology Clinical Research RN Sr.- Flower Mound Texas Oncology

Postdoctoral Research Associate University of Texas at Dallas

Dallas Clinical Research Project Coordinator Medpace Holdings Inc

Study Start Up Coordinator - Clinical Research Coordinator Experience Medpace Holdings Inc

Clinical Research Coord 1 Baylor Scott & White Health

Dallas Clinical Research Project Coordinator Medpace, Inc.

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

Research Scheduler IQVIA Holdings Inc

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

Director Analyst, Research & Development Gartner Inc

Project Manager, Research and Data Workflow American Heart Association

Experience Research Senior Associate JPMorgan Chase & Co

Research Coordinator IQVIA Holdings Inc

Lead Research Engineer Thomson Reuters Corp

Research Technician I University of Texas at Dallas

Senior Market Research Consultant HCSC

Clinical Study Manager Argon Medical Devices Inc

Director, Clinical Site Velocity Clinical Research, Inc.

Clinical Trial Project Manager Ophthalmology Dallas Medpace Holdings Inc

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

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

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

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

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

Ophthalmic Medical Assistant / Plano Texas Retina Associates

Grant Proposal Manager, Clinical American Heart Association

Director, Clinical Site Velocity Clinical Research Inc

Medical Billing AR Analyst Texas Oncology

Associate Clinical Trial Manager PhD Postdoctoral Infectious Diseases Dallas Medpace Holdings Inc

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

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

Associate Physician Pinnacle Fertility Inc.

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

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 - Metabolic - 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.

Program Implementation Manager, Clinical Studies American Heart Association

Medical Director - Molecular Oncology & Genomics Quest Diagnostics Inc

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