Clinical Research Coordinator III

Location 330 N Rufe Snow Drive,Keller, TX, 76248,United States Employee Type Non-Exempt - FT Job Title Clinical Research Coordinator III FLSA Classification Non-Exempt Reports to Site Operations Manager This position will float between Keller, Dallas, and Flower Mound, with Keller as the home base Job Summary/ Objective The Clinical Research Coordinator III 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 a health-related field Experience 3 years' experience in Clinical Research preferred Skills Regulatory Filing and accessing documents, Study Submission Assistant, Conduct close-out visits Finance Stipend payments Subject Interaction Recruit, interview, screen, enroll, and randomize subjects Collect medical history Conduct study visits Administrative EDC Query resolution AE/SAE documentation and reporting Address protocol violations and deviations Order supplies Clinical Skills Vital Signs ECG 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. May 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 This job description may not be inclusive of all assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of the Employer. #J-18808-Ljbffr Helios Clinical Research