In-house Clinical Research Associate II - U.S. - Remote

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Requirements:

• Bachelor’s Degree or a Nursing Degree required
• Minimum of two years experience as an In-House CRA or Clinical Research Coordinator (CRC)
• Proficiency in Microsoft Office, CTMS, and EDC Systems

Responsibilities:

• Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
• Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
• Perform feasibility studies/site identification activities for potential sites, as requested