Licensed Clinical Social Worker Or Licensed Clinical Counsler/Phycologist Commonwealth Medical ServicesLicensed Clinical Social Worker Or Licensed Clinical Counsler/PhycologistEuless, TXCommonwealth Medical Services is seeking a compassionate and dedicated Licensed Clinical Social Worker (LCSW) or Licensed Clinical Counselor/Psychologist to join our esteemed team in the Hospital & Health Care industry. As a key member of our healthcare team, you will engage with clients to assess their mental health needs, develop personalized treatment plans, and implement evidence-based interventions to promote their emotional and psychological well-being.
Clinical Research Coordinator II Pinnacle Clinical ResearchClinical Research Coordinator IIFarmers Branch, TexasComplete 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. Summary: The Clinical Research Coordinator II 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.
Academic Professional Track (Non-Tenure): Clinical Assistant Professor or Clinical Associate Professor Texas A&M UniversityAcademic Professional Track (Non-Tenure): Clinical Assistant Professor or Clinical Associate ProfessorDallas, TXThe faculty member will: Lead and contribute to the behavioral science curriculum across the DDS and dental hygiene programs, including instruction in health behavior theory, motivational interviewing, patient communication, cultural competence, and social determinants of oral health, etc. The Department of Public Health Sciences in the College of Dentistry at Texas A&M University invites applications for a full time 100%FTE, academic professional track (non-tenure) faculty position with an 11-month service period; the start date is August, 2026, or negotiable.
Clinical Research Regulatory Specialist Baylor Scott & White HealthClinical Research Regulatory SpecialistDallas, TXThis includes protocol revisions or amendments for new treatments, administrative changes, subject population changes, funding, recruitment, site changes, informed consent changes, or dual enrollment. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits.
Clinical Research Associate II/III - US Optimapharm ddClinical Research Associate II/III - USDallas, TXRemoteWith operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. As we expand our US Clinical Operations team, we're searching for a CRA II/III who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives.
Clinical Research Coordinator II - Mansfield, TX Iterative HealthClinical Research Coordinator II - Mansfield, TXMansfield, TexasWe built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Clinical Research Coordinator Wake ResearchClinical Research CoordinatorDallas, TXAs of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).
Clinical Research Coordinator II ObjectiveHealthClinical Research Coordinator IIDallas, TXNot easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
Clinical Research Coordinator II - Mansfield, TX Iterative Scopes Inc.Clinical Research Coordinator II - Mansfield, TXMansfield, TXThis role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success. Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
Clinical Research Coord 1 Baylor Scott & White HealthClinical Research Coord 1Plano, TXPerforms research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met. Examples include providing in-service education for healthcare professionals and working with Pharmacy to ensure smooth project flow.
Pediatric Phlebotomist/Clinical Research Assistant General AccountsPediatric Phlebotomist/Clinical Research AssistantMesquite, TexasSMS Clinical Research is seeking an experienced Pediatric Phlebotomist who will also work as a Clinical Research Assistant to join our growing clinical research team. This is an excellent opportunity for a highly skilled phlebotomist who enjoys working with infants, children, and families and is interested in expanding their experience in clinical research.
Clinical Research Systems Specialist Iterative HealthClinical Research Systems SpecialistSouthlake, TX$23–$40 / hourA Clinical Research Systems Specialist at Iterative Health plays an important role in enabling our clinical research operations by ensuring the systems, study builds, and operational materials that support our trials are accurate, efficient, and ready for use by our teams and research sites. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Pediatric Phlebotomist/Clinical Research Assistant Salma Mazhar MD PAPediatric Phlebotomist/Clinical Research AssistantMesquite, TXFull timeSMS Clinical Research is seeking an experienced Pediatric Phlebotomist who will also work as a Clinical Research Assistant to join our growing clinical research team. This is an excellent opportunity for a highly skilled phlebotomist who enjoys working with infants, children, and families and is interested in expanding their experience in clinical research.
Clinical Regulatory Specialist Iterative HealthClinical Regulatory SpecialistSouthlake, TXYou will collaborate with site teams, internal stakeholders, sponsors, CROs, IRBs, and other external partners to ensure regulatory requirements are completed accurately, efficiently, and in accordance with applicable guidelines and study requirements. Working under the direction of a Clinical Regulatory Manager Director, you will partner closely with clinical research sites to manage regulatory activities throughout the study lifecycle—from study start-up and activation through ongoing maintenance and closeout.
Clinical Trial Project Manager - Immunology - Dallas Medpace, Inc.Clinical Trial Project Manager - Immunology - DallasIrving (Dallas), TexasJob 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. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Trial Project Manager - Neuroscience - Dallas Medpace, Inc.Clinical Trial Project Manager - Neuroscience - DallasIrving (Dallas), TexasWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. 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.
Clinical Trial Project Manager - Ophthalmology - Dallas Medpace, Inc.Clinical Trial Project Manager - Ophthalmology - DallasIrving (Dallas), TexasJob 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. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Trial Project Manager - Dallas, TX Medpace, Inc.Clinical Trial Project Manager - Dallas, TXIrving (Dallas), TexasWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. 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 .
Clinical Trial Project Manager - Infectious Diseases - Dallas Medpace, Inc.Clinical Trial Project Manager - Infectious Diseases - DallasIrving (Dallas), TexasResponsibilities: 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.
Clinical Research Systems Specialist Iterative Scopes Inc.Clinical Research Systems SpecialistSouthlake, TXA Clinical Research Systems Specialist at Iterative Health plays an important role in enabling our clinical research operations by ensuring the systems, study builds, and operational materials that support our trials are accurate, efficient, and ready for use by our teams and research sites. Familiarity with clinical trial documentation, including study budgets, Clinical Trial Agreements (CTAs), eCRF guidelines, lab manuals, pharmacy manuals, informed consent forms, and annotated CRFs.