Clinical Research Associate II IREClinical Research Associate IIDallas, TexasWilling and able to travel up to 50% for on-site monitoring visits across south region; preference given to candidates residing in Dallas, Texas near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Systems Specialist Iterative Scopes IncClinical 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.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorDallas, TX$32–$36 / hourThis position focuses on research participant recruitment and consenting, delivering concierge-level service throughout the clinical trial journey, and coordinating biospecimen collection in collaboration with clinical research nursing, laboratory teams, and hospital departments. The Clinical Research Coordinator II (Non-RN) plays a key role in all aspects of clinical research, including screening and enrolling participants, coordinating their care and follow-up, and ensuring strict adherence to regulatory and protocol requirements.
Clinical Investigator SGS SAClinical InvestigatorRichardson, TXWrites protocols, collects and reviews data, prepares progress reports, analyzes results, writes summaries and conclusions and issues reports. Interfaces with the Sponsor, staff, contractors, professional societies, Institutional / Investigational Review Board (IRB), subjects, government agents / agencies and other business units.
Clinical Regulatory Specialist Iterative Scopes IncClinical 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.
NewPre-Clinical Research Associate Orano SAPre-Clinical Research AssociatePlano, TXRemoteOrano's activities in the U.S. include developing uranium enrichment facility in Oak Ridge, TN; packages and transportation of uranium & nuclear fuel assemblies; fabricating & installing used nuclear fuel dry storage canisters and casks, conducting pool-to-pad used nuclear fuel transfers; providing solutions to the National Labs and to the Dept of Energy; and supplying U.S. nuclear energy utilities with uranium, conversion, and enrichment services. Name Pre-Clinical Research Associate Ref # 16520 Posting date Friday, September 25, 2026 Country United States Region Texas City Plano Business Unit (BU) CORP Type of Employment Permanent/Regular Desired Starting Date 19-10-2026 Work Schedule Full time Remote Work In office Job N - LABORATORY.
NewDallas Clinical Research Project Coordinator Medpace, Inc.Dallas Clinical Research Project CoordinatorIrving (Dallas), TexasResponsibilities: 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. 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.
NewClinical Quality Program Manager Elevance Health IncClinical Quality Program ManagerGrand Prairie, TXCandidates should possess exceptional organizational, project management, and communication skills, with demonstrated ability to manage multiple priorities, coordinate across diverse stakeholder groups, and drive complex initiatives to successful completion. Minimum requirements: Requires a BS in health administration, nursing, or a related clinical field; 4 years of health care quality or data analysis experience; or any combination of education and experience, which would provide an equivalent background.
Clinical Informatics Analyst Medpace Holdings IncClinical Informatics AnalystIrving, TXBachelor's in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to prioritize multiple projects on a sprint schedule; Excellent verbal communication skills; Programming experience in R or Python; Work experience with clinical data; Experience building web applications is preferred (with either Shiny or Streamlit); and. 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.
NewStudy Start-Up Coordinator – Clinical Research Coordinator Experience Medpace, Inc.Study Start-Up Coordinator – Clinical Research Coordinator ExperienceIrving (Dallas), TexasResponsibilities: 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. 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.
Cryo Nerve Block Clinical Specialist - Dallas AtriCure IncCryo Nerve Block Clinical Specialist - DallasDallas, TXCryo Nerve Block Clinical Specialist - Dallas. Ho Chi Minh City, Ho Chi Minh, Vietnam.
NewClinical Data Manager I Cook Children's Health Care SystemClinical Data Manager IFort Worth, TXThis individual interprets, abstracts, and submits comprehensive, accurate data relating to study subjects by abstracting data as required by the study protocol and/or clinical trial sponsor, verifies and updates all information compiled and enter data into the application in a timely manner, and performs coding of adverse events or other designed medical diagnosis, injury, and/or procedures as directed by protocol, as required. 9+ years of combined relevant healthcare experience (degree can be substituted with equivalent clinical healthcare or research experience).
NewAssociate Manager, Mako Clinical Processes, Southwest Stryker CorpAssociate Manager, Mako Clinical Processes, SouthwestDallas, TXRemote$98,200–$163,700 / yearWorks actively with FEES, CONNECT Leads and MPS Managers to create scalable metrics for reporting to Senior Manager of Mako Clinical Processes and Stryker Sales leadership on what "success" looks like during and after onboarding new MPS hires. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
CTRC Clinical Research Nurse University of Texas at DallasCTRC Clinical Research NurseRichardson, TXMonitor research participants during protocol-directed procedures; recognize abnormal findings, symptoms, adverse events, or other safety concerns; and promptly notify the appropriate investigator, Medical Director, or other designated research personnel in accordance with study and CTRC procedures. The Research Nurse may actively participate in research participant recruitment and education and works collaboratively with the Medical Director, principal investigators, physicians, research coordinators and administrators, laboratory personnel, and other members of the research team.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceTXTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedTXTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Informatics Analyst Medpace, Inc.Clinical Informatics AnalystIrving (Dallas), TexasBachelor’s in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to prioritize multiple projects on a sprint schedule; Excellent verbal communication skills; Programming experience in R or Python; Work experience with clinical data; Experience building web applications is preferred (with either Shiny or Streamlit); and. 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.
RN Home Health Clinical Case Manager - ProHealth Home Health (Addison, TX) ProHealth Home Health & HospiceRN Home Health Clinical Case Manager - ProHealth Home Health (Addison, TX)Addison, TexasShe/he supervises home health services to homebound patients in their place of residence in accordance with attending physician orders and plans of care and strives to provide the highest quality of care. The Clinical Manager is available at all times during operating hours (or appoints a similarly qualified alternate) and participates in all activities relevant to professional services furnished, including the development of qualifications and assignment of personnel.
NewPrior Authorization Clinical Pharmacist Elevance HealthPrior Authorization Clinical PharmacistGrand Prairie, TXUnless expressly allowed by state or federal law, or regulation, must be located in a state or territory of the United States when conducting utilization review or an appeals consideration and cannot be located on a US military base, vessel or any embassy located in or outside of the US, unless they are command-sanctioned activities. For URAC accredited areas, the following professional competencies apply: Associates in this role are expected to have strong oral, written and interpersonal communication skills, problem-solving skills, facilitation skills, and analytical skills.
Clinical Research Associate II, Phase I - Texas/Mid-West Fortrea IncClinical Research Associate II, Phase I - Texas/Mid-WestDallas, TXRemote$100,000–$120,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.