NewRN Hospice Admissions/Clinical Liaison - $10,000 Sign-On Bonus! AccentCare, Inc.RN Hospice Admissions/Clinical Liaison - $10,000 Sign-On Bonus!Houston, TX$95,000–$105,000 / yearJoin AccentCare as a Clinical Liaison VIPC, Inpatient Hospice Admissions RN, where you’ll serve as a trusted resource for patients, families, and healthcare partners — helping ensure those who need hospice care receive timely, compassionate support. As a Clinical Liaison VIPC, Inpatient Hospice Admissions RN, you will play a key role in identifying patient needs and facilitating seamless transitions into hospice services.
Clinical - Clinical Pharmacist 1 - 210392 Pacer GroupClinical - Clinical Pharmacist 1 - 210392Houston, TXRemote$60–$65In this role, you will review prior authorization and appeal requests to help ensure members receive the right medications based on clinical guidelines and health plan policies. You will work with healthcare providers, pharmacy technicians, and internal teams to make accurate and timely coverage decisions.
Research Coordinator II - Cancer - Clinical Trials Clinical Studies Houston Methodist HospitalResearch Coordinator II - Cancer - Clinical Trials Clinical StudiesHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
Part time Clinical Nurse - Clinical & Translational Research Center University of Texas MD Anderson Cancer CenterPart time Clinical Nurse - Clinical & Translational Research CenterHouston, TXWith a 41-bed treatment area and a full-function laboratory, the 12,660-square-foot CTRC provides a dedicated environment for first-in-human and Phase I and II clinical research where innovation meets patient care. The Clinical & Translational Research Center (CTRC) is the hub for groundbreaking early-phase clinical trials, supporting more than 700 cutting-edge studies across 22 departments.
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote Merck & Co IncClinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- RemoteHouston, TXRemote$96,200–$151,400 / yearRequired Skills: Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies, Data Analysis, Data Reporting, Early Clinical Development, Policy Development, Preventive Action, Protocol Adherence, Regulatory Compliance, Site Management. Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Clinical Nurse - Clinical & Translational Research Center University of Texas MD Anderson Cancer CenterClinical Nurse - Clinical & Translational Research CenterHouston, TXSpecific competencies include: IV insertion and venous access device management; Accurate administration and monitoring of infusions via a variety of routes (oral, subcutaneous, intramuscular, intravenous); Performing an independent double-check for chemotherapy administration; Safe handling and disposal of chemotherapy to minimize patient and staff exposure to hazardous drugs; Management of treatment-related side effects and adverse reactions; Minimizing the risk for infection among patients who are actually or potentially immunocompromised; Knowledge needed to facilitate early detection of specific side effects that lead to effective self-management of the side effect when it does occur. Advanced Cardiac Life Support (ACLS) certification and Pediatric Advanced Life Support (PALS) certification if working in the following department: Nrsg Post Anesthesia Care Unit (600160).
Assistant Professor, Clinical Faculty Appointment (CFA) - Clinical Cancer Prevention MD AndersonAssistant Professor, Clinical Faculty Appointment (CFA) - Clinical Cancer PreventionHouston, TXThis position will provide clinical services primarily at MD Anderson's Cancer Prevention Center locations, including the Texas Medical Center - Fannin, Northwest Houston, and Missouri City, with designated protected time allocated for research and educational activities. The Clinical Cancer Prevention Department is a multidisciplinary department whose members conducts basic, translational, and cancer prevention clinical research, and provides clinical cancer prevention services and education.
Clinical Trial Program Manager - Neurology (Neurodegenerative division) University of Texas Health Science Center at HoustonClinical Trial Program Manager - Neurology (Neurodegenerative division)Houston, TXRegistered Nurse (RN) State Licensure or Nurse Licensure Compact (NLC) by Texas Board of Nursing (BON) depending on clinical trial, may be required Human Subjects Research (HSR) by Collaborative Institutional Training Initiative (CITI Program) depending on clinical trial, may be requiredMinimum Education:Bachelor''s Degree required In the event that an RN degree is required, the bachelor''s degree may be waivedMinimum Experience:5 years of relevant experience required Pharmaceutical or clinical research strongly preferredPhysical Requirements:Exerts up to 100 pounds of force occasionally and/or up to 50 pounds frequently and/or up to 20 pounds constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Sr. Clinical Research Nurse - Transplant Center Houston Methodist HospitalSr. Clinical Research Nurse - Transplant CenterHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Assists Principal Investigator to ensure that all persons 'engaged' in research studies have met training requirements in accordance with Federal regulations and entity policies and procedures including preparing Institutional Review Board (IRB) and regulatory documents following ICH/GCP guidelines, and the development of materials and tools necessary to appropriately facilitate the conduct of research.
NewManager, Clinical Radiology PRN - Neuroradiology University of Texas Health Science Center at HoustonManager, Clinical Radiology PRN - NeuroradiologyHouston, TXCertified Medical Radiologic Technologist (MRT) by Texas Medical Board (TMB) requiredRadiography (R) by American Registry of Radiologic Technologists (ARRT) requiredBasic Life Support (BLS) by American Heart Association (AHA) requiredMinimum Education:Associate''s Degree in Radiography, Clinical Radiation Science or related field requiredMinimum Experience:5 years of directly related experience required Experience with WBCT preferredPhysical Requirements:Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Clinical Research Specialist (Neurology Department) Houston Methodist HospitalClinical Research Specialist (Neurology Department)Houston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols, gathering patient data via methods specified in the study protocol, study reports.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Houston, TexasFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
NewSenior Manager, Clinical Trial Program - Neurology (Stroke Institute) University of Texas Health Science Center at HoustonSenior Manager, Clinical Trial Program - Neurology (Stroke Institute)Houston, TXRegistered Nurse (RN) State Licensure or Nurse Licensure Compact (NLC) by Texas Board of Nursing (BON) depending on clinical trial may be required Human Subjects Research (HSR) by Collaborative Institutional Training Initiative (CITI Program) may be requiredMinimum Education:Bachelor''s Degree required In the event that an RN degree is required, Bachelor''s degree may be waivedMinimum Experience:7 years of relevant experience required Pharmaceutical or clinical research strongly preferredPhysical Requirements:Exerts up to 100 pounds of force occasionally and/or up to 50 pounds frequently and/or up to 20 pounds constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Clinical Research Administrator - Pediatrics TMC University of Texas Health Science Center at HoustonClinical Research Administrator - Pediatrics TMCHouston, TXCertification/Skills: NoneMinimum Education:Bachelor''s Degree in Healthcare Administration, Business, Finance, Accounting, or related degree requiredMinimum Experience:3 years of related experience requiredPhysical Requirements:Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Senior Clinical Research Associate (Texas Region) Axsome TherapeuticsSenior Clinical Research Associate (Texas Region)Houston, TXOur industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, agitation associated with dementia due to Alzheimer's disease, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, as well as multiple novel product candidates addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Reporting to the Senior Manager of Clinical Monitoring, theSenior CRA will be responsible for site management and monitoring activities at assigned sites across assigned programs ensuring the trial is conducted in compliance with the protocol, ICH/GCP, applicable regulatory requirements and applicable SOPs/Work Instructions.
Clinical Research Assistant Alcanza Clinical Research LLCClinical Research AssistantKaty, TXResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Clinical Research Coordinator II - Nurse Iterative Scopes IncClinical Research Coordinator II - NurseWebster, TXBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorKaty, TXScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Clinical Research Assistant/ Medical Assistant Alcanza Clinical ResearchClinical Research Assistant/ Medical AssistantKaty, TexasResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Clinical Research Nurse - Transplant Center Houston Methodist HospitalClinical Research Nurse - Transplant CenterHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.