1,004 programming-"https:"-"FEMTO-ST"-"UCL" "https:" "https:" "https:" "https:" "https:" "inserm" positions at Stony Brook University
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experience or a combination of higher education and experience totaling four years may be considered. Seven (7) years of full-time experience in plan review and/or project administration. Current certification
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which would provide training equivalent to that given in a training, apprenticeship, or equivalent program, or an equivalent combination of experience and training gained by completion of technical
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training equivalent to that given in a training, apprenticeship, or equivalent program, or an equivalent combination of experience and training gained by completion of technical courses in the electrical
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would provide training equivalent to that given in a training, apprenticeship, or equivalent program, or an equivalent combination of experience and training gained by completion of technical courses in
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Job Description Required Qualifications (as evidenced by an attached resume): Attorney approved to practice law in NYS. Three (3) years of full-time responsible experience in program development
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-service needs of the staff and the implementation of an effective orientation program. Qualifications Required Qualifications: NYS Registered Nurse License. Clinical practice experience working with
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attending and/or supporting events, activities, and programs sponsored by areas within and outside the Office of Student Life (i.e., campus-wide traditions, events, programs). Other duties or projects as
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, they conduct in-service education programs relating to theories and techniques of phlebotomy, and perform related clerical work. Duties of a Phlebotomists may include the following but are not limited
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would provide training equivalent to that given in a training, apprenticeship, or equivalent program, or an equivalent combination of experience and training gained by completion of technical courses in
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Investigator/Cancer Clinical Trials Administrative Director. Includes screening, eligibility, data collection, adverse event reporting, completion of CRF's and all regulatory requirements per protocol. Plan and