Hiring: Clinical Research Coordinator Company: The START Center for Cancer Research Location: Fort Worth, TX Job Posted Time: 2026-09-17 10:54:19 Target Skills & Keywords : GCP, Microsoft Office About the job Experience: •2 years of clinical research experience. •Basic understanding of oncology clinical trials, particularly Phase 1 studies. •Strong attention to detail and accuracy in data collection and documentation. •Solid functional working knowledge of GCP and regulatory requirements. •Proficient in Microsoft Office Suite and clinical trial management software. Required Skills: •Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol. •Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study. •Create/review forms created or revised for assigned trials to assure protocol compliance. •Maintain files using standardized study document labeling and filing procedures. •Implement initial protocol and amendments, training staff who will be involved in patient treatment and management. •Assist with patient screening and determination of eligibility. •Facilitate the informed consent process ensuring that consent is appropriately completed. •Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations. Qualifications: •High School Diploma or GED. Compensation: •Flexible work environment (work from home / hybrid options) •Competitive benefits and rewards package •401(k) retirement savings plan with employer match Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!