Clinical Research Coordinator III

Location 300 N Rufe Snow Drive,Keller, TX, 76248,United States Employee Type Non-Exempt - FT J ob Title : Clinical Research Coordinator I I I FLSA Classification: Non - Exempt Reports to: Site Operations Manager Job Summary / Objective : The Clinical Research Coordinator I I I is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager Essential Functions : Overseeing Clinical Trials: Ensure trouble-free running of clinical trials. Monitor study participants’ health throughout the trial. Compile reports summarizing the success or failure of drugs, technologies, or medical procedures Oversee 5+ trials Data Collection and Analysis: Collect data obtained from research. Participant Interaction: Communicate with study participants regarding study objectives . Monitor participant adherence to study rules. Collaboration and Compliance: Liaise with laboratories Monitor study compliance with protocols and ethical standards. Ensure adherence to regulatory requirements. Record Keeping: Maintain research records, including case report forms and drug dispensation records. Direct specimen collection, labeling, storage, and transport. Logistics and Supplies: Ensure all necessary equipment and supplies are in stock and functional. Education/Experience/Skills Education : Bachelor's degree preferred in health-related field Experience : 3 years experience in Clinical Research preferred Skills: Filing and accessing documents, Study Submission Assistant , Conduct Close out Visits Finance Stipend payme nts Subject Interaction Recruit, interview, screen , enroll , and randomize subjects Collect medical history Conduct study visits Administrative EDC Query resolution AE/SAE documentation and reporting Ad d ress protocol violations and deviations Order supplies Clinical Skills Vital Sign s

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Study Management Conduct PSSV’s and SIV’s Complete Feasibility Questionnaires Manage trials from start to closeout Working Conditions / Physical Demands: Standard operating hours are Monday through Friday, 8:00 a.m. to 5 : 00 p.m . M ay be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour work week . Requires prolonged walking, standing, some bending , stooping, and stretching . Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment . Requires normal range of hearing and eyesight to record, prepare , and communicate appropriate reports . Travel required: as needed (travel to IM’s may be required ) Disclaimer T his job description may not be inclusive of all assigned duties, responsibilities , or aspects of the jo b described , and may be amended at any time at the sole discretion of the Employer #J-18808-Ljbffr Jimmy Jazz