393 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Edinburgh Napier University" positions at Baylor College of Medicine
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to identify potential study participants, coordinate sample collection and data entry, liaise with collaborating sites, and maintain regulatory compliance. The position requires strong skills in organization
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the daily activities of clinical research studies. Key responsibilities include participant screening, enrollment, and follow‑up; ensuring accurate and timely data collection and documentation; and
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Independently carry out research projects. Participate in lab management and supervision/training of junior lab members. Prepare and conduct laboratory research experiments. Collect, compile and analyze data. May
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Status: Exempt Work Schedule: Monday – Friday, 8 a.m. – 5 p.m. Summary The Texas Children’s Cancer and Hematology Centers (TXCH) Data Manager/Clinical Research Associate is responsible for implementing and
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bioinformatics/data analysis, to join our multidisciplinary research team at Baylor College of Medicine. The Postdoctoral Associate will work on cutting-edge translational cancer research projects that involves
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research experiments within the Pediatric Brain Tumor Research Program. This position will be responsible for evaluation and analyzing large sequencing and multiome data-sets. Baylor College of Medicine
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Coordinator I. This role involves managing day-to-day study activities, including participant screening, enrollment, monitoring, data management, and coordinating study visits. The initial appointment is one
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Work Schedule: Monday – Friday, 8 a.m. – 5 p.m. Summary We are seeking an innovative AI Engineer to join our team at the Baylor College of Medicine and Texas Children's Hospital Data Science Center where
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. Collaborates with biostatistics faculty and team members to develop data analysis plans. Uses statistical software to create programs for data management, manipulation, and standard/advanced analysis. Performs
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patient enrollment, screening, monitoring of research participants, and reporting to the clinical research sponsor. Responsible for ensuring accurate data collection, documentation, organization and safety