Description Sr. Clinical Trials Specialist-Neurology JOB SUMMARY: Responsible for the timely preparation, planning and quality control of regulatory documents required for human subjects research. Oversees the preparation and submission of national and international applications and ongoing reports for clinical trials approvals and renewals. Collaborates with all levels of scientific, medical and technical staff to support regulatory strategies, policies and procedures. Interfaces with national and international regulatory agencies and industry sponsors in the approval of Phase I, II, III, and IV clinical studies. Department Summary:
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