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. Participate in departmental quality, safety, and patient experience initiatives. Maintain timely and accurate clinical documentation in the electronic medical record. Education and Supervision Supervise and
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position operates primarily in a professional office environment and requires extended periods of computer use, document review, and participation in in person and virtual meetings. The role involves regular
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, Skills, and Abilities Excellent written, verbal and computer skills required. Excellent communication and interpersonal skills. Must be able to work independently and/or collaboratively. Excellent critical
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: The candidate will work primarily in Newark, NJ and/or New Brunswick, NJ with some remote flexibility. Candidate will have access to a standard computer, phone, and internet access to perform the duties
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Must be a current Rutgers student. Certifications/Licenses Required Knowledge, Skills, and Abilities Effective oral and communication skills. Must be computer literate with proficiency and working
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commitment to quality. Familiarity with Trial Master File (TMF) or electronic Trial Master File (eTMF) systems. Preferred Qualifications Experience managing multicenter clinical trials or complex clinical
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Abilities Excellent communication and analytical skills required. Strong spreadsheet and personal computer skills required. Able to work under deadlines and to balance multiple projects. Preferred
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proficiently. Hearing is essential. The ability to focus on the task at hand despite numerous interruptions. Must be able to sit for extended periods of time and document into an electronic medical record
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. Preferred Qualifications Minimum of one (1) year of lab research experience is highly preferred, but is not required. A basic knowledge of computer programming, particularly with MATLAB and/or LabVIEW is
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forms; counsels patients regarding paperwork requirements. Maintains Computer Databases entering changes in demographic, insurance, and other information as required. Collects co pays, and posts in