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Clinical Trial Coordinator - Regulatory Documents/ TMF

Company: Tech Observer
Location: New York
Posted on: May 17, 2018

Job Description:

Summary: Basic understanding of clinical study processes, with specialized technical skills to deliver own work within the clinical study team. Effectively manages time to meet project deliverables and deadlines in a manner that minimizes rework. Takes appropriate care to ensure quality of data. Keeps team and supervisor informed and up-to-date on information directly related to own position in the clinical operations study team. Required: Bachelor's degree in relevant scientific discipline preferred. Minimum of 3 years in Pharmaceutical Company with relevant experience. Must possess strong Microsoft Excel and other computer skills. Experience in Oncology preferred. General knowledge of basics of clinical operations. Familiarity and experience with Regulatory Documents/TMF Possible experience with assisting with invoice processing/budgetary support (not oversight)

Keywords: Tech Observer, New York, Clinical Trial Coordinator - Regulatory Documents/ TMF, Healthcare, New York, New York

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