23 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"Dr" positions at Temple University in United States
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research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations. As a Clinical Research Coordinator
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Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study
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clinical research projects such as preparing IRB submissions, screening and enrolling participants into research studies, and collecting and entering study data using Good Clinical Practice techniques
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Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study
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letter addressing qualifications. Curriculum vitae. Statement of teaching philosophy. Statement of contributions working effectively in an urban environment Contact information for 3-5 professional
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study data. *Perform various research, database, and clerical tasks to support clinical trials, aiding investigators in organizing, gathering, and compiling clinical research data. *Organize and maintain
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information, contact Cheri Carter at cheri.carter@temple.edu. Application review begins immediately and will continue until the position is filled. Temple University is an equal opportunity/affirmative action
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training meetings as required by study project *Demonstrated computer skills, and proficiency with MS Office Suite software programs. *Excellent written and verbal communication skills *Patient facing
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; administrative operation of the department, disseminating information, and handling confidential information; provides directions to student workers. In addition, the Administrative Specialist will be responsible
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and conduct study visits *Collect and enter data; register subjects and study visits in OnCore *Perform Epic research billing review *Maintain an up-to-date regulatory binder *Schedule and attend