NewBriefing and Research Attorney JobotBriefing and Research AttorneyHouston, TX$90,000–$110,000 / yearOver the years our client has gone from being the go-to auto, trucking, and on-the-job injury firm in Texas to becoming a nationally-recognized personal injury practice handling all types of accident claims and representing clients in mass tort, personal injury, product liability, child injury, and whistleblower protection cases nationwide as one of the largest law firms. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
NewBilingual Clinical Research Coordinator I (English/Spanish) Johnson County ClintrialsBilingual Clinical Research Coordinator I (English/Spanish)Houston, TXBy applying advanced knowledge of study protocols, strong organizational skills, and sound judgment, the Clinical Research Coordinator I contributes to the timely, efficient, and high-quality conduct of clinical studies that advance research objectives and improve patient outcomes. The purpose of the Clinical Research Coordinator I role is to ensure the successful execution of multiple concurrent clinical trials through effective study coordination, subject management, and cross-functional communication.
NewBilingual Clinical Research Coordinator II (English and Spanish) Johnson County ClintrialsBilingual Clinical Research Coordinator II (English and Spanish)Houston, TXBy applying advanced knowledge of study protocols, strong organizational skills, and sound judgment, the Clinical Research Coordinator II contributes to the timely, efficient, and high-quality conduct of clinical studies that advance research objectives and improve patient outcomes. The purpose of the Clinical Research Coordinator II role is to ensure the successful execution of multiple concurrent clinical trials through effective study coordination, subject management, and cross-functional communication.
NewClinical Research Coordinator Pinnacle Clinical ResearchClinical Research CoordinatorHouston, TXComplete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs. Job Description Summary: The Clinical Research Coordinator will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are followed.
NewClinical Research Coordinator - Onsite - North Houston Advanced Rheumatology of HoustonClinical Research Coordinator - Onsite - North HoustonSpring, TXIn this hands-on role, you will help coordinate clinical trials involving autoimmune, inflammatory, and rheumatologic conditions while working closely with patients, investigators, sponsors, and clinical research partners. Our growing private rheumatology practice in The Woodlands, Texas, is seeking a motivated and highly organized Clinical Research Coordinator (CRC) to join our research team.
NewClinical Research Coordinator aQua DialysisClinical Research CoordinatorHouston, TXConcrete background in medicine· Thorough knowledge of medical research· Excellent verbal and written communication skills· Proficiency with computers, especially Microsoft office· Knowledgeable about ICH Guidelines, GCPs, as well as FDA regulations· Able to handle multiple protocols in various therapeutic areas· Must be detailed oriented· Must be willing to travel to various locations in Greater Houston Education Experience· Bachelors required, Master degree preferred.· Maintains strict patient confidentiality according to HIPAA regulations and applicable law.· Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs guidelines· Contribute to growth of company with future supervisory role REQUIREMENTS:· Great at customer service· Self-motivated/starter· Outgoing, excellent recruiting skills· Phlebotomy experiences a MUST.·
NewClinical Trial Research Assistant Advanced Rheumatology of HoustonClinical Trial Research AssistantSpring, TXWoodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. Preferred Skills: Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
NewClinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorSugar Land, 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;].
NewMedical Technologist - MRIT - Lab/Research Tech Accountable Healthcare StaffingMedical Technologist - MRIT - Lab/Research TechHouston, TXJob Description Medical Technologist - Immediate and Future Travel / Local Contracts and Per Diem Availability - Start Date: ASAP / Medical Technologist - MRIT - Lab/Research Tech / Travel Contract DISRUPTING THE TYPICAL AGENCY MODEL . Our efforts to provide growth opportunities both for our clinician and internal employees allowed Accountable to be singled out and recognized as an outstanding employer in the healthcare industry.
NewClinical Research Coordinator HOUSTON REGIONAL GASTROENTEROLOGY INSTITUClinical Research CoordinatorKaty, TXThis role requires the ability to independently manage up to five active study protocols simultaneously while ensuring high-quality study execution and regulatory compliance. Potentially supervise staff at assigned research sites, including: Managing daily workflow and task delegation.
NewClinical Research Psychometric Rater Tekton Research IncClinical Research Psychometric RaterHouston, TXConducting a variety of psychometric rating scales on subjects with various diagnoses (such as ADHD, Alzheimer's Disease, Bipolar Disorder, GAD, Major Depressive Disorder, Post Traumatic Stress Disorder, Substance Use Disorders, Epilepsy, Anxiety Disorders, and Schizophrenia/Schizoaffective Disorder) for our clinical trials, in compliance with specific study protocols, FDA, GCP, ICH, and privacy guidelines. The Psychometric Rater will be responsible for interviewing research participants and their informants/caregivers, who are being evaluated to participate in a research study for various health conditions, in compliance with study protocol, SOPs, GCP, ICH, and FDA Regulations.
NewClinical Research Infusion Nurse INTEGRITY ADVANCED THERAPEUTICS PLLClinical Research Infusion NurseHouston, TXThe Clinical Research Infusion Nurse plays a critical role in the execution of clinical trials by safely administering investigational medications or placebos to study participants. Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
NewResearch Assistant World Research LinkResearch AssistantHouston, TXOn a typical day, a Research Assistant may help prepare for participant visits, confirm appointments, organize study materials, perform approved prescreening, obtain vital signs, prepare laboratory kits, process specimens, enter data, maintain research records, assist with recruitment, and prepare documents requested by a clinical trial monitor. A Research Assistant helps ensure that research visits are organized, study documentation is complete, participants receive professional and attentive support, and clinical trial activities are performed according to the study protocol, Good Clinical Practice (GCP), ICH guidelines, World Research Link SOPs, and applicable regulatory requirements.
NewClinical Research Coordinator (CRC) One of a Kind Clinical Research Center LLCClinical Research Coordinator (CRC)Houston, TXThis position is embedded within a clinical practice and offers the opportunity to work closely with patients, physicians, and research teams to advance clinical trials. As a newer site, we move with purpose and passion — building a team that's collaborative, community-connected, and committed to making a real impact in the world of clinical research.
NewClinical Research Assistant Horizon Clinical ResearchClinical Research AssistantCypress, TXThe CRA will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical research timeline from pre-site visit (PSV) through study close-out. Work closely with Principal Investigators (PIs) to assure subjects receive appropriate medical evaluation and care.
NewClinical Research Assistant Pinnacle Clinical ResearchClinical Research AssistantHouston, TXAlways maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties. Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.
NewClinical Research Coordinator -Traveling PRN Alcanza Clinical ResearchClinical Research Coordinator -Traveling PRNSugar Land, TXResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 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; Scheduling 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. Skills, Knowledge and Expertise Minimum Qualifications : A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.
NewClinical Research Coordinator (CRC) LINQ Research, LLCClinical Research Coordinator (CRC)Pearland, TXThis position is ideal for a CRC who has previously taken ownership of clinical studies, interfaced directly with study monitors and sponsors, and can confidently manage patient visits, data integrity, investigational product accountability, and study activities with minimal oversight. The CRC will work closely with the Site Manager, Principal Investigator, Investigators, Recruitment, Regulatory, sponsors, CROs, and study monitors and will serve as a primary point of contact for study participants, sponsors, and monitors.
NewBusiness Development Manager - Clinical Research LINQ Research, LLCBusiness Development Manager - Clinical ResearchPearland, TX$90,000–$115,000 / yearThis individual should be proactive, resilient under pressure, and target-driven when opportunities move slowly or prospects decline, consistently generate new pipeline rather than simply maintain existing relationships, and bring either an established network or a demonstrated ability to rapidly build one within the clinical research and site-management industry. This position will develop and execute business development strategies, establish and monitor departmental KPIs, coach and develop Business Development Associates, identify and engage new physician and Principal Investigator prospects, build Sponsor and CRO relationships, and generate new clinical trial opportunities.
NewClinical Research Coordinator (CRC)-FT Evolution Research GroupClinical Research Coordinator (CRC)-FTHouston, TXMaintain organized, accurate and complete study records including but not limited to regulatory documents, signed informed consents, IRB correspondence/approvals, source documentation, drug dispensing logs, subject logs and study-related communications. In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.