Clinical Research Assistant II — Internal Medicine Trials
University of Texas Southwestern Medical Center
UT Southwestern Medical Center is seeking a Clinical Research Assistant II to support multiple clinical studies by recruiting, screening, consenting, enrolling, and following participants. You will coordinate study visits, explain procedures, and manage data through CRFs, EDC systems, and EPIC, while supporting lab activities and QA/QC checks. You will also assist with regulatory documentation, study startup and closeout, and provide operational support to the CRA Lead and study teams. #J-18808-Ljbffr University of Texas Southwestern Medical Center
- UT Southwestern Medical Center is seeking a Clinical Research Data Specialist to support trauma-focused trials. You will manage study databases, track participant visits, and prepare data summaries for measurement-based care. The role involves data entry, regulatory documentation...Suggested
- ...‑renowned medical and research center, we strive to provide... ...‑treatment/treatment) trials/studies. May provide... ...direction of the PI, Clinical Research Coordinator... ...The Clinical Research Assistant II serves as a... ...formal sponsor audits or internal audits. Recruits and enrolls...SuggestedFull timeLocal area
- UT Southwestern Medical Center in Dallas, TX seeks a Research & Laboratory professional to support data management for local and national... ...under supervision of investigators, coordinating observational trials and managing study databases for the CTRN. Responsibilities...SuggestedLocal area
- ..., global Contract Research Organisation (CRO)... ..., patient-focused clinical development. We specialise... ...for a CRA II/III who is... ...hope for patients International projects and professional... ...clinical trial monitoring experience... .../institutions and assist with the execution...SuggestedFull timeContract workInterim roleRemote workWorldwide
- SGS is seeking a Clinical Research Assistant II (Contract) on call for 6-8 weeks in Richardson, TX. You will support study procedures in the clinic and perform related administrative duties to assist coordinators, following GCP guidelines and SOPs. Responsibilities include...SuggestedContract work
- Clinical Research Assistant II (Contract) - On Call - 6-8 weeks This is a Contract position. We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600...Contract workWork experience placementWork at officeFlexible hoursDay shiftAfternoon shift
- ...innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources... ...under minimal supervision to provide responsible technical assistance in performance of assignments requiring basic knowledge of...Full timePart timeShift work
- ...Overview Job Summary: Coordinate various research trials for the Institute for Global Health, including early or late phase FDA-regulated... ...regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial patient data...Full timeWork at officeMonday to Friday
- ...laboratories, working together to enable a better, safer and more interconnected world. Job Description ~ Performs daily clinic tasks to assist coordinators with study procedures. Tasks may include but are not limited to Electronic Self-Assessment Questionnaire (ESAQ...Full timeWork experience placementWork at office
- SGS North America Inc. is seeking an Administrative/Clinic Support role to assist coordinators with study procedures and daily clinic tasks in a fast-paced environment. Responsibilities include preparing materials, coordinating appointments, QC of study documents, and maintaining...
- ...an alternative application process. Clinical Research Assistant Full Time Dallas, TX, US Summary:... ...allowable limits defined within clinical trials protocols, standard operating... ...Food and Drug Administration (FDA), International Council for Harmonization Good Clinical...Full timeTemporary workWork at officeLocal areaFlexible hours
- ...SummaryJoin our CRA Team in Dallas, Texas!The Clinical Research Associate position offers an exciting... ...levels of CRAOpportunity to work with international team of CRAsResponsibilitiesConduct... ...) through our integrated Clinical Trial Management System to identify site deviations...Contract workWork experience placementWork at officeLocal areaImmediate startRemote work
- Job SummaryExperienced Clinical Research Associate (CRA) - join our growing team!Medpace is growing... ...levels of CRAOpportunity to work with international team of CRAsResponsibilitiesConduct... ...) through our integrated Clinical Trial Management System to identify site deviations...Contract workWork at officeRemote workWork from home
- Summit Clinical Research Solutions in Dallas, TX is seeking a Clinical Research Assistant to support the Clinical Research Coordinator and principal investigator in administering clinical trial activities, ensuring confidentiality and adherence to FDA, ICH GCP, HIPAA,...
- Clinical Research Associate (CRA) - Dallas Join to apply for the Clinical... ...Coordinators Research Assistants MEDPACE CRA TRAINING PROGRAM... ...CRA, CRA Manager, Clinical Trial Manager, Training and Development... ...Opportunities to work with international team of CRAs....Contract workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
- ...Description Job Description Summary: Assists the Clinical Research Coordinator and the principal... ...allowable limits defined within clinical trials protocols, standard operating... ...Food and Drug Administration (FDA), International Council for Harmonization Good Clinical...Temporary workWork at officeLocal areaFlexible hours
$19.23 - $23.08 per hour
...Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed... ...development of life-changing medicines. Our mission is simple... ...Clinical Research Assistant role at our Dallas... ...supervision of a CRC II, CRC III, or Site Manager...Hourly payWork at officeFlexible hours- ...Engineering backgrounds for the CRA role!The Clinical Research Associate position offers an exciting... ...levels of CRAOpportunity to work with international team of CRAsResponsibilitiesConduct... ...) through our integrated Clinical Trial Management System to identify site deviations...Contract workWork experience placementWork at officeRemote workWork from home
- ...Upstate Medical University in Syracuse, NY seeks a Clinical Research Associate I to coordinate Oncology trials across the Cancer Center and satellites, handling investigational meds and radiation therapy in early to late FDA-regulated studies. You will ensure federal compliance...
$60.41k - $65k
...Job Summary: TheClinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in human through phase 3 trials.... ...study volunteers, collecting detailed clinical information and communicating that to...Full timeMonday to FridayFlexible hoursAfternoon shift- ...Engineering backgrounds for the CRA role! The Clinical Research Associate position offers an exciting... ...of CRA ~ Opportunity to work with international team of CRAs Responsibilities... ...) through our integrated Clinical Trial Management System to identify site deviations...Contract workWork experience placementWork at officeRemote workWork from homeHome officeFlexible hours
$60.4k - $68k
...Job Summary: SUNY Upstate Research Foundation is seeking an Clinical Research Associate I to coordinate various research trials for the Department of Urology, i ncluding early to late phase FDA regulated trials. Key Responsibilities: Ensure compliance with...Full timeWork at officeMonday to Friday$62.34k - $65k
...Job Summary: The Clinical Research Associate I will coordinate Oncology research trials for the Cancer Center and associated satellite sites, primarily involving investigational medications and radiation therapy, including early or late phase FDA-regulated trials....Full timeWork at officeMonday to Friday$18 - $24 per hour
About The Role To support U.S Urology Partners by assisting the research department with patient care needs and treatment appointments. What... ...healthcare insurance verification and pre-authorization process Clinical administration skills Electronic Medical Records...Work at officeLocal areaNight shift$18 - $24 per hour
## Clinical Research AssistantApplylocations: Syracuse, NYtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R3127**About the Role**To support U.S Urology Partners by assisting the research department with patient care needs and treatment appointments....Hourly payWork at officeLocal areaNight shift- ...Clinical Research Associate - Cross Therapeutic Area - Dallas ICON plc is a world-leading healthcare intelligence and clinical research... ...progress and escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as...Remote jobLocal areaVisa sponsorshipFlexible hours
- UT Southwestern Medical Center in Dallas, TX is seeking a Clinical Research Assistant (Emergency Medicine) to support multiple studies in a fast-paced ED setting. You will collect data, coordinate visits, and help ensure regulatory compliance while maintaining participant...
- The University of Texas Southwestern Medical Center in Dallas is seeking a Clinical Research Assistant I in Emergency Medicine to support multiple studies. You will collect and manage data, screen participants, obtain informed consent, and ensure regulatory compliance in...
- ...individual to perform administrative and clinical tasks to support study coordinators.... ...relevant experience. Responsibilities include assisting with study procedures, preparing test... ...environment and the opportunity to contribute to important clinical research. #J-18808-Ljbffr SGS
- ...United States. Responsibilities include on-site service, troubleshooting down to component level, and accurate documentation. A technical college degree with 2+ years' field service experience is required; clinical device experience is a plus. #J-18808-Ljbffr Laborie
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