169 data "https:" "https:" "https:" "https:" "Dr" "L2CM" positions at Temple University
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participants, obtain informed consent, administer questionnaires, collect urine and blood samples, and assist with specimen processing and perform data management. The CRC will be involved with all day-to-day
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communication messaging. The position also requires the ability to interpret and communicate data to inform messaging strategies and assess communication effectiveness. Creative and design skills are considered a
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allows the team members to communicate much more effectively and share information, improving the quality of care for each patient. The team at the Center of Hope is devoted to providing optimal care
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studies, and biochemical interaction assays. Demonstrated success in developing innovative genome engineering strategies. Strong research management and project coordination skills, including rigorous data
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*Establish and maintain databases of subjects *Schedule and conduct study visits *Collect and enter data; register subjects and study visits in OnCore *Perform Epic research billing review *Maintain an up
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visits, coordinating and performing research-related tests, data collection, data entry and regulatory submissions (IRB). This position will play a critical part in the success of the clinical trials and
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the ability to be detail-oriented and to handle multiple tasks. 4)Strong written and verbal communication skills. 5)Demonstrated computer skills, along with the ability to operate standard office equipment and
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philosophy. Statement of contributions working effectively in an urban environment Contact information for 3 professional references. Apply at academic jobs online Equal Employment Opportunity Statement Temple
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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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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