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Clinical research specialist

Company: Global Channel Management, Inc.
Location: Irvine
Posted on: October 12, 2019

Job Description:

Clinical research specialist needs 2 years experience in clinical research Clinical research specialist requires: Strong working experience with XML, XSD, JSON, and other formats candidate with prior experience as Study Start-Up Specialist but not mandatory bachelors in life sciences or related field Knowledge, Skills, and Abilities Knowledge of FDA regulations required. Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook Experience with Adobe Acrobat Professional and Microsoft Access a plus Written and Oral Communication Presentation Delivery Planning and Organizing Decision Making, Judgment, and Problem Solving People Relationships, Influencing Others, Motivating Employees, Team Building Initiative and Accountability Proven ability to interact with different functional groups Ability to easily adapt to a changing environment Clinical research specialist duties: Capable of performing all of the activities and responsibilities with direction of the Site Start-Up Unit Manager, Global Monitoring Operations: Director, Associate Director, or designee Monitor project plans and communicates and troubleshoots the leading and lagging indicators to meet Site Initiation Readiness at the Investigator Meeting. Manage information sharing (i.e. Site Start-Up tracker, Site Identification Tracking Tools). Train study team members on current process and study execution modalities Estimated travel may be 10%.

Keywords: Global Channel Management, Inc., Irvine , Clinical research specialist, Healthcare , Irvine, California

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