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limited to Phase I-IV clinical trials. The Clinical Research Regulatory Specialist C will, independently prepare and process all regulatory documentation/applications through the IRB and requisite ancillary
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domains of psychology. Primals research is now flourishing, with dozens of investigations in labs around the world. Looking forward, the Primals Project will adapt and reprise the mapping process for
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Responsibilities: Clinical Research Coordinator B Prepare and process all Institutional Review Board (IRB)through the IRB and other regulatory groups as appropriate including initial submissions, amendments
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systems subject matter expert. Manage and process requests to hire or reappoint staff, faculty, postdocs, students, temporary workers, and consultants. Responsible for job board postings, employee data
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success of the PPRC sample repository. Job Responsibilities Independently manage PPRC sample repository: receive samples, organize, process, store, and ship human biospecimen from PPRC studies Manage
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the School's research mission. Manage and coordinate the electronic proposal submission process for Principal Investigators; maintain knowledge of complex processes and continually changing sponsor guidelines
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further investigation into variances. This position maintains a key role in the annual budget process, including consultation with Senior Management and the Provost office, in preparation of the budget
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the School’s research mission. Manage and coordinate the electronic proposal submission process for Principal Investigators; maintain knowledge of complex processes and continually changing sponsor guidelines
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, personnel, and related record-keeping functions. This position will maintain and update the payroll and personnel system, process monthly and weekly payroll, run payroll reports, and manage related
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for developing and executing process validation protocol for aNDA product. 2) Perform quality control testing and production of aNDA products and become subject matter expert in aNDA product. 3) Initiate